Category: 109-12-6

Pyrimidine is an aromatic heterocyclic organic compound similar to pyridine. 109-12-6, formula is C4H5N3, Name is Pyrimidin-2-amine. In nucleic acids, three types of nucleobases are pyrimidine derivatives: cytosine (C), thymine (T), and uracil (U). Name: Pyrimidin-2-amine.

Sebestyen, Zoltan;Jakab, Emma;Doman, Andrea;Bokrossy, Peter;Bertoti, Imre;Madarasz, Janos;Laszlo, Krisztina research published 《 Thermal degradation of crab shell biomass, a nitrogen-containing carbon precursor》, the research content is summarized as follows. Waste and low-cost lignocellulosic biomasses are well studied and widely used as raw materials for porous carbon adsorbents. Much less attention is given to the exploration of the potential of marine biomasses, though these materials contain also nitrogen, which-if preserved during the processing-has a beneficial influence on the sorption properties of the porous carbon obtained. Here, we report a multi-technique investigation into the conversion of crab shell to porous carbon adsorbent. Thermogravimetry and pyrolysis-GC/MS studies were used to reveal the thermal degradation of this natural polymer and follow the decomposition process through the identification of the products. Almost 40 various volatile degradation products were distinguished released at 500°C pyrolysis temperature Based on the TGA/DTG results, two temperatures, 350 and 500°C, were selected to obtain pyrolytic samples in macroscopic quantities in order to characterize the morphol. and surface chem. of the solid fraction. More than 50% of the nitrogen atoms were still in the carbonaceous matrix after the 500°C pyrolysis in the C-N=C, C-NH and 3C-N-type bonds. The ash content < 1% included hydroxylapatite-type crystalline matter. Based on these results, we may conclude that crab shells have a high potential as precursor of nitrogen-containing biochar.

Name: Pyrimidin-2-amine, 2-Aminopyrimidine is a useful research compound. Its molecular formula is C4H5N3 and its molecular weight is 95.1 g/mol. The purity is usually 95%.
2-Aminopyrimidine is an organic compound that belongs to the group of pyridines. It has been shown to have antimicrobial, antitumor, and antiviral properties. 2-Aminopyrimidine has been used as a fungicide and herbicide in horticulture and agriculture, respectively. The molecular geometry of this molecule is octahedral with coordination geometry C2v. This chemical binds to the BCR-ABL kinase receptor and inhibits its activity by competitive inhibition of ATP binding. 2-Aminopyrimidine has been shown to have a hematologic response in vivo models and in vitro assays. It also has anti-inflammatory effects when it is taken orally or applied topically., 109-12-6.

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Pyrimidine is a nitrogenous base similar to benzene (a six-membered ring) and includes cytosine, thymine, and uracil as bases used for DNA or RNA. 109-12-6, formula is C4H5N3, Name is Pyrimidin-2-amine. Pyrimidine also found in many synthetic compounds such as barbiturates and the HIV drug, zidovudine. Application In Synthesis of 109-12-6.

Puckowska, Anna;Gawel, Magdalena;Komorowska, Marlena;Drozdzal, Pawel;Arning, Aleksandra;Pawelski, Damian;Brzezinski, Krzysztof;Plonska-Brzezinska, Marta E. research published 《 Synthesis and Structural Characterization of Pyridine-2,6-dicarboxamide and Furan-2,5-dicarboxamide Derivatives》, the research content is summarized as follows. This work aimed to obtain a series of sym. pyridine-2-6-dicarboxamides I (Ar = pyrazin-2-yl, pyridin-4-yl, 3-nitrophenyl, etc.) and furan-2,5-dicarboxamides II through a condensation reaction of the appropriate acyl chlorides such as 2,5-furandicarbonyl dichloride, 2,6-pyridinedicarbonyl dichloride and aromatic amines ArNH₂. The crystal structures were solved for seven compounds; two pyridine derivatives I (Ar = pyridin-4-yl, 4-aminophenyl) and five furan derivatives II (Ar = pyrimidin-5-yl, pyridin-4-yl, pyridin-3-yl, 1,3-thiazol-2-yl, 3-nitrophenyl). Based on this crystallog. studies were able to indicate supramol. features of the crystals under investigation. Addnl., Hirshfeld surface anal. allowed to calculate a distribution of intermol. contacts in the dicarboxamide crystals.

109-12-6, 2-Aminopyrimidine is a useful research compound. Its molecular formula is C4H5N3 and its molecular weight is 95.1 g/mol. The purity is usually 95%.
2-Aminopyrimidine is an organic compound that belongs to the group of pyridines. It has been shown to have antimicrobial, antitumor, and antiviral properties. 2-Aminopyrimidine has been used as a fungicide and herbicide in horticulture and agriculture, respectively. The molecular geometry of this molecule is octahedral with coordination geometry C2v. This chemical binds to the BCR-ABL kinase receptor and inhibits its activity by competitive inhibition of ATP binding. 2-Aminopyrimidine has been shown to have a hematologic response in vivo models and in vitro assays. It also has anti-inflammatory effects when it is taken orally or applied topically., Application In Synthesis of 109-12-6

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Pyrimidine is an aromatic heterocyclic organic compound similar to pyridine. One of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring), it has the nitrogen atoms at positions 1 and 3 in the ring. 109-12-6, formula is C4H5N3, Name is Pyrimidin-2-amine. The pyrimidine ring system has wide occurrence in nature as substituted and ring fused compounds and derivatives, including the nucleotides cytosine, thymine and uracil, thiamine (vitamin B1) and alloxan. Application In Synthesis of 109-12-6.

Rai, Sunil K.;Baidya, Debjani;Nangia, Ashwini K. research published 《 Salts, solvates and hydrates of the multi-kinase inhibitor drug pazopanib with hydroxybenzoic acids》, the research content is summarized as follows. The marketed formulation of pazopanib (PAZ) suffers from low and variable bioavailability because of its poor dissolution rate and photostability issues. The drug falls under Biopharmaceutics Classification System (BCS) class II of low solubility and good permeability. The hydrogen bonds and supramol. interactions in crystalline forms of PAZ with hydroxybenzoic acids (HBAs) and dihydroxybenzoic acids (DHBAs), as well as its salts are analyzed. Ten X-ray crystal structures of PAZ which include the reference drug, a THF solvate (PAZ·THF) and eight salts with HBAs/DHBAs are reported. There is proton transfer from the carboxylic group of the coformer acid to the most basic nitrogen atom of the 2-aminopyrimidine ring of PAZ in all cases. Two salts were crystallized in neat form, while the remaining six are solvates and hydrates. The crystal structure of PAZ is stabilized by sulfonamide and 2-aminopyrimidine homosynthons of N-H···O and N-H···N hydrogen bonds in an R22(8) ring motif. PAZ·HBA/DHBA salts consistently contain the aminopyridinium···carboxylate N+-H···O- synthon of the R22(8) ring. The sulfonamide homosynthon of PAZ is disrupted in preference to the formation of N-H···O and N-H···N hydrogen bonds in salt structures. The presence of an addnl. basic nitrogen atom in the indazole ring of PAZ promotes hydration and solvation through the O-H···N hydrogen bond. Whereas the formation of salts is desirable for pharmaceutical formulation, the inclusion of adventitious solvent and/or water mols. with hydroxybenzoic acid coformers in the cocrystal-salt products is a limitation for this class of coformers. The stability problem faced with hydrates and solvates of PAZ·HBA/DHBA salts means that their formation must be carried out by strictly anhydrous procedures. The consistent occurrence of the aminopyridinium···carboxylate N+-H···O- ring synthon is discussed in relation to the previous results of Aakeroy, Nangia and Zaworotko groups on similar acid-base multi-component systems.

Application In Synthesis of 109-12-6, 2-Aminopyrimidine is a useful research compound. Its molecular formula is C4H5N3 and its molecular weight is 95.1 g/mol. The purity is usually 95%.
2-Aminopyrimidine is an organic compound that belongs to the group of pyridines. It has been shown to have antimicrobial, antitumor, and antiviral properties. 2-Aminopyrimidine has been used as a fungicide and herbicide in horticulture and agriculture, respectively. The molecular geometry of this molecule is octahedral with coordination geometry C2v. This chemical binds to the BCR-ABL kinase receptor and inhibits its activity by competitive inhibition of ATP binding. 2-Aminopyrimidine has been shown to have a hematologic response in vivo models and in vitro assays. It also has anti-inflammatory effects when it is taken orally or applied topically., 109-12-6.

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

The systematic study of pyrimidines began in 1884 with Pinner, who synthesized derivatives by condensing ethyl acetoacetate with amidines. Pinner first proposed the name “pyrimidin” in 1885. 109-12-6, formula is C4H5N3, Name is Pyrimidin-2-amine. The parent compound was first prepared by Gabriel and Colman in 1900, by conversion of barbituric acid to 2,4,6-trichloropyrimidine followed by reduction using zinc dust in hot water. Synthetic Route of 109-12-6.

Rani, Sudesh;Luxami, Vijay;Paul, Kamaldeep research published 《 Synthesis of Triphenylethylene-Naphthalimide Conjugates as topoisomerase-II α inhibitor and HSA binder》, the research content is summarized as follows. A series of triphenylethylene-naphthalimide (TPE-naph) conjugates I [R = morpholin-4-yl, cyclohexylamino, butylamino, benzylamino, etc.] was synthesized by a mol. hybridization technique, and their anticancer activity was evaluated in vitro on 60 human cancer cell lines through their cytotoxicity. The ratios of E and Z isomers were determined on the basis of HPLC methodol. and NMR spectroscopy. The structure-activity relationship for anticancer activity was deduced on the basis of the nature and bulkiness of the amine attached to the C-4 position of the naphthalene ring. Exptl. and mol. modeling studies of the most active TPE-naph conjugate bearing a morpholinyl group showed that it was able to inhibit topoisomerase-II (TOPO-II) as a possible intracellular target. Moreover, the transportation behavior of TPE-naph conjugate towards human serum albumin (HSA) indicated efficient binding affinity. The steady-state and time-dependent fluorescent results suggested that this conjugate quenched HSA significantly through static as well as dynamic quenching. Thus, this report discloses the scope of TPE-naph conjugates I as efficient anticancer agents.

Synthetic Route of 109-12-6, 2-Aminopyrimidine is a useful research compound. Its molecular formula is C4H5N3 and its molecular weight is 95.1 g/mol. The purity is usually 95%.
2-Aminopyrimidine is an organic compound that belongs to the group of pyridines. It has been shown to have antimicrobial, antitumor, and antiviral properties. 2-Aminopyrimidine has been used as a fungicide and herbicide in horticulture and agriculture, respectively. The molecular geometry of this molecule is octahedral with coordination geometry C2v. This chemical binds to the BCR-ABL kinase receptor and inhibits its activity by competitive inhibition of ATP binding. 2-Aminopyrimidine has been shown to have a hematologic response in vivo models and in vitro assays. It also has anti-inflammatory effects when it is taken orally or applied topically., 109-12-6.

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

The pyrimidine ring system has wide occurrence in nature as substituted and ring fused compounds and derivatives, 109-12-6, formula is C4H5N3, Name is Pyrimidin-2-amine. including the nucleotides cytosine, thymine and uracil, thiamine (vitamin B1) and alloxan. HPLC of Formula: 109-12-6.

Rehan, Thamer A.;Al-Lami, Naeemah;Khudhair, Noor Ali research published 《 Synthesis, characterization and anti-corrosion activity of new triazole, thiadiazole and thiazole derivatives containing imidazo[1,2-a]pyrimidine moiety》, the research content is summarized as follows. In this research, several heterocyclic rings (triazole, thiadiazol, thiazol) containing imidazo (1,2-a) pyrimidine moiety have been prepared via a series of reactions. To do this, synthesis of 2-substituted imidazo (1,2-a) pyrimidine was performed by condensation of 2-aminopyrimidine with (4-bromo phenacyl bromide) or (4-Ph phenacyl bromide). Carbaldehyde group was prepared at position-3 of 2-substituted imidazo/pyrimidine rings by Vilsmeier-Haak reaction. Thiosemicarbazon derivatives (Schiff bases) were synthesized by condensation of 3-carbaldehyde derivatives with thiosemicarbazide. Cyclization of thiosemicarbazone derivatives with Ac₂O, 4-bromophenacyl bromide and HCl afforded the corresponding thiadiazole(diacetyl) derivatives, 1,3-thiazole derivatives and 1,2,4-triazole derivatives resp. Structures of the new derivatives were confirmed via FT-IR spectroscopy, some of which were confirmed via 1H-NMR spectroscopy. Three of these new derivatives were evaluated by their anti-corrosion activity.

HPLC of Formula: 109-12-6, 2-Aminopyrimidine is a useful research compound. Its molecular formula is C4H5N3 and its molecular weight is 95.1 g/mol. The purity is usually 95%.
2-Aminopyrimidine is an organic compound that belongs to the group of pyridines. It has been shown to have antimicrobial, antitumor, and antiviral properties. 2-Aminopyrimidine has been used as a fungicide and herbicide in horticulture and agriculture, respectively. The molecular geometry of this molecule is octahedral with coordination geometry C2v. This chemical binds to the BCR-ABL kinase receptor and inhibits its activity by competitive inhibition of ATP binding. 2-Aminopyrimidine has been shown to have a hematologic response in vivo models and in vitro assays. It also has anti-inflammatory effects when it is taken orally or applied topically., 109-12-6.

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

The systematic study of pyrimidines began in 1884 with Pinner, who synthesized derivatives by condensing ethyl acetoacetate with amidines. Pinner first proposed the name “pyrimidin” in 1885. 109-12-6, formula is C4H5N3, Name is Pyrimidin-2-amine. The parent compound was first prepared by Gabriel and Colman in 1900, by conversion of barbituric acid to 2,4,6-trichloropyrimidine followed by reduction using zinc dust in hot water. Product Details of C4H5N3.

Rehan, Thamer A.;Al-Lami, Naeemah;Alanee, Rafal Shakeeb research published 《 Anti-cancer and antioxidant activities of some new synthesized 3-secondary amine derivatives bearing imidazo[1,2-a]pyrimidine》, the research content is summarized as follows. In this study, new series of 2-aryl-3-(pyrimidin-2-ylamino)imidazo[1,2-a]pyrimidine derivatives I (R = H, Br, NO₂, OH, NH₂; R¹ = H) were synthesized through one-pot reaction of aromatic ketones 4-RC₆H₄C(O)Me and 2-aminopyrimidine. These reactions were performed in the presence of I₂ and DMSO. Derivatives of 3-amine compound I were reacted with propargyl bromide to yield 2-phenyl-N-(prop-2-yn-1-yl)-N-(pyrimidin-2-yl) derivatives of imidazo/pyrimidine rings. I (R¹ = CH₂CCH). Then, by Mannich reaction, one of 3-secondary amine derivatives I (R = NH₂, R¹ = H) was reacted with different aromatic amines to form Mannich bases II (R² = benzo[d]thiazol-2-ylamino, morpholino, 2-methoxy-4-nitrophenylamino, etc.). Other derivatives of imidazo(1,2-a)pyrimidine I (R = NO₂, R¹ = H; R = NO₂, R¹ = CH₂CCH; R = NHCH₂CCH, R¹ = CH₂CCH), II (R² = 2-methoxy-4-nitrophenylamino) were evaluated for anti-oxidant activity and one of these derivatives I (R = NHCH₂CCH, R¹ = CH₂CCH) was tested for cytotoxic activity against breast cancer using MTT assay.

Product Details of C4H5N3, 2-Aminopyrimidine is a useful research compound. Its molecular formula is C4H5N3 and its molecular weight is 95.1 g/mol. The purity is usually 95%.
2-Aminopyrimidine is an organic compound that belongs to the group of pyridines. It has been shown to have antimicrobial, antitumor, and antiviral properties. 2-Aminopyrimidine has been used as a fungicide and herbicide in horticulture and agriculture, respectively. The molecular geometry of this molecule is octahedral with coordination geometry C2v. This chemical binds to the BCR-ABL kinase receptor and inhibits its activity by competitive inhibition of ATP binding. 2-Aminopyrimidine has been shown to have a hematologic response in vivo models and in vitro assays. It also has anti-inflammatory effects when it is taken orally or applied topically., 109-12-6.

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

The pyrimidine ring system has wide occurrence in nature as substituted and ring fused compounds and derivatives, including the nucleotides cytosine, thymine and uracil, thiamine (vitamin B1) and alloxan. 109-12-6, formula is C4H5N3, Name is Pyrimidin-2-amine. It is also found in many synthetic compounds such as barbiturates and the HIV drug, zidovudine. Formula: C4H5N3.

Ostrovsky, Serghei research published 《 Magnetostructural study of four-coordinated Co(II) complexes with mixed ligand surrounding》, the research content is summarized as follows. The dependence of the zero-field splitting parameters on the structural modification of the nearest ligands surrounding in the [CoCl₂L₂] complexes (with L being the N-donor ligand) is studied. The modification was modeled by the variations of the NCoN and ClCoCl angles, by the rotation of the chlorido ligands with respect to other ligand groups as well as by the strength of the N-donor ligands. The found tendency was compared with the exptl. data for this type of cobalt complexes known from literature.

Formula: C4H5N3, 2-Aminopyrimidine is a useful research compound. Its molecular formula is C4H5N3 and its molecular weight is 95.1 g/mol. The purity is usually 95%.
2-Aminopyrimidine is an organic compound that belongs to the group of pyridines. It has been shown to have antimicrobial, antitumor, and antiviral properties. 2-Aminopyrimidine has been used as a fungicide and herbicide in horticulture and agriculture, respectively. The molecular geometry of this molecule is octahedral with coordination geometry C2v. This chemical binds to the BCR-ABL kinase receptor and inhibits its activity by competitive inhibition of ATP binding. 2-Aminopyrimidine has been shown to have a hematologic response in vivo models and in vitro assays. It also has anti-inflammatory effects when it is taken orally or applied topically., 109-12-6.

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Pyrimidine is an aromatic heterocyclic organic compound similar to pyridine. One of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring), it has the nitrogen atoms at positions 1 and 3 in the ring. 109-12-6, formula is C4H5N3, Name is Pyrimidin-2-amine. The pyrimidine ring system has wide occurrence in nature as substituted and ring fused compounds and derivatives, including the nucleotides cytosine, thymine and uracil, thiamine (vitamin B1) and alloxan. Quality Control of 109-12-6.

Panigrahi, Ahwan;Sharanappa Sherikar, Mahadev;Ramaiah Prabhu, Kandikere research published 《 ZnBr₂ Mediated C-N Bond Formation using Cinnamyl Alcohol and 2-Amino Pyridines》, the research content is summarized as follows. A simple method for C-N bond formation is disclosed by using cinnamyl alcs. and 2-amino pyridine derivatives in the presence of stoichiometric amount of zinc bromide. This reaction works with a wide range of substrates, and is compatible with primary, secondary, and homoallylic alcs. To the best of our knowledge, this is the first report for C-N bond formation using cinnamyl alc. and 2-amino pyridines using zinc bromide as a Lewis acid.

109-12-6, 2-Aminopyrimidine is a useful research compound. Its molecular formula is C4H5N3 and its molecular weight is 95.1 g/mol. The purity is usually 95%.
2-Aminopyrimidine is an organic compound that belongs to the group of pyridines. It has been shown to have antimicrobial, antitumor, and antiviral properties. 2-Aminopyrimidine has been used as a fungicide and herbicide in horticulture and agriculture, respectively. The molecular geometry of this molecule is octahedral with coordination geometry C2v. This chemical binds to the BCR-ABL kinase receptor and inhibits its activity by competitive inhibition of ATP binding. 2-Aminopyrimidine has been shown to have a hematologic response in vivo models and in vitro assays. It also has anti-inflammatory effects when it is taken orally or applied topically., Quality Control of 109-12-6

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

The systematic study of pyrimidines began in 1884 with Pinner, who synthesized derivatives by condensing ethyl acetoacetate with amidines. Pinner first proposed the name “pyrimidin” in 1885. 109-12-6, formula is C4H5N3, Name is Pyrimidin-2-amine. The parent compound was first prepared by Gabriel and Colman in 1900, by conversion of barbituric acid to 2,4,6-trichloropyrimidine followed by reduction using zinc dust in hot water. Recommanded Product: Pyrimidin-2-amine.

Panigrahi, Uttam Kumar;Bhat, Venugopal T.;Ramakrishnan, Vengadesh Kumara Mangalam research published 《 Magnetically Recyclable Heterogeneous Cobalt Ferrite Catalyst for the Direct N-Alkylation of (Hetero)aryl Amines with Alcohols》, the research content is summarized as follows. Herein we report the use of spinel cobalt ferrite nanoparticles as an efficient and selective catalyst for the mono N-alkylation of aryl and hetero aryl amines with various aromatic and aliphatic alcs. Based on our experiments, the optimum condition for good to excellent yield were observed with alc. (1.0 mmol), aniline (1.2 mmol), KOH (0.5 equiv), and CoFe2O4 nanocatalyst (10 mol%) in toluene at 130°C in 24 h. Further control experiment studies revealed that the reaction does not proceed in the absence of the catalyst or a strong base. This magnetically recyclable nanocatalyst does not require any ligands and is easily synthesized at low temperature The reutilization of the recovered catalyst in a fresh reaction gave good to excellent yield. The experiment results strongly suggest a borrowing hydrogen pathway for N-alkylation under our standard conditions. The utility of these nanocatalysts was also demonstrated for the dehydrogenative synthesis of heterocycles like indole and quinolines.

Recommanded Product: Pyrimidin-2-amine, 2-Aminopyrimidine is a useful research compound. Its molecular formula is C4H5N3 and its molecular weight is 95.1 g/mol. The purity is usually 95%.
2-Aminopyrimidine is an organic compound that belongs to the group of pyridines. It has been shown to have antimicrobial, antitumor, and antiviral properties. 2-Aminopyrimidine has been used as a fungicide and herbicide in horticulture and agriculture, respectively. The molecular geometry of this molecule is octahedral with coordination geometry C2v. This chemical binds to the BCR-ABL kinase receptor and inhibits its activity by competitive inhibition of ATP binding. 2-Aminopyrimidine has been shown to have a hematologic response in vivo models and in vitro assays. It also has anti-inflammatory effects when it is taken orally or applied topically., 109-12-6.

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Pyrimidine is a nitrogenous base similar to benzene (a six-membered ring) and includes cytosine, thymine, and uracil as bases used for DNA or RNA. 109-12-6, formula is C4H5N3, Name is Pyrimidin-2-amine. Pyrimidine also found in many synthetic compounds such as barbiturates and the HIV drug, zidovudine. SDS of cas: 109-12-6.

Pankratova, E. V.;Portseva, T. N.;Makarova, A. A.;Ilyin, Yu. V.;Stepchenko, A. G.;Georgieva, S. G. research published 《 Glycogen synthase kinase 3 Inhibitor, CHIR, Suppress Transcription of Tissue Specific POU2F1 Isoform in Burkitt Namalwa Lymphoma Cells》, the research content is summarized as follows. POU2F1 (Oct-1) is a transcription factor, the overexpression of which is found in many human malignant tumors; a significant increase in its level in cells determines the malignant potential of the tumor. POU2F1 is represented in cells by several isoforms that are transcribed from alternative promoters. In Burkitt’s B-cell lymphoma Namalwa, the concentration of tissue-specific isoform Oct-1L is several times higher than in normal B cells. We tested the potential to inhibit the transcription of individual Oct-1 isoforms using the GSK3 kinase inhibitor CHIR, an aminopyrimidine derivatives We have shown that CHIR specifically affects the expression of the tissue-specific isoform Oct-1L, significantly reducing the level of mRNA and Oct-1L protein. However, CHIR does not change the amount of mRNA and protein of the ubiquitous isoform Oct-1A in Namalwa tumor cells. The results obtained show that it is possible to develop a system for selective inhibition of Oct-1 transcription factor isoforms in human cells to suppress drug resistance of tumor cells with a high POU2F1 content.

109-12-6, 2-Aminopyrimidine is a useful research compound. Its molecular formula is C4H5N3 and its molecular weight is 95.1 g/mol. The purity is usually 95%.
2-Aminopyrimidine is an organic compound that belongs to the group of pyridines. It has been shown to have antimicrobial, antitumor, and antiviral properties. 2-Aminopyrimidine has been used as a fungicide and herbicide in horticulture and agriculture, respectively. The molecular geometry of this molecule is octahedral with coordination geometry C2v. This chemical binds to the BCR-ABL kinase receptor and inhibits its activity by competitive inhibition of ATP binding. 2-Aminopyrimidine has been shown to have a hematologic response in vivo models and in vitro assays. It also has anti-inflammatory effects when it is taken orally or applied topically., SDS of cas: 109-12-6

Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia