Category: 908240-50-6

Related Products of 908240-50-6 ,Some common heterocyclic compound, 908240-50-6, molecular formula is C7H3Cl2N3, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route.

2,4-Dichloropyrido[3,4-d]pyrimidine (49.8 g, 250 mmol),28percent ammonia (94g, 750mmol was added to a flask containing 500mL of ethanol,The reaction was stirred for 48 hours with stirring at room temperature.TLC monitors the endpoint of the reaction.The precipitated solid was filtered, and the ethanol was rinsed.Drying gave Compound 16-1 (27 g, yield 60percent).

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,908240-50-6, its application will become more common.

Reference:
Patent; Beijing Dingcai Technology Co., Ltd.; Gu’an Dingcai Technology Co., Ltd.; Sun Entao; Liu Song; Xing Qifeng; Zhang Xianghui; (189 pag.)CN109020975; (2018); A;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 908240-50-6, name is 2,4-Dichloropyrido[3,4-d]pyrimidine, the common compound, a new synthetic route is introduced below. Recommanded Product: 908240-50-6

A mixture of 2,4-dichloropyrido[3,4-d]pyrimidine (250 mg, 1.25 mmol), 4-(1H- pyrazol-4-yl)aniline (199, 1.25 mmol), and iPr2NEt (0.44 mL, 2.50 mmol) in DIVIF (2.5 mL) was heated at 100 C for 5h, cooled to rt, and diluted with water. The precipitate formed was collected by filtration and washed with water and dried in vacuo to provide the title compound (400 mg,99%). MS 19S+) m/e 323 (M+H) .

The synthetic route of 908240-50-6 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; KADMON CORPORATION, LLC; OLSZEWSKI, Kellen; POYUROVSKY, Masha; BARSOTTI, Anthony; KIM, Ji-In; LIU, Kevin; MORRIS, Koi; (143 pag.)WO2016/210331; (2016); A1;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 908240-50-6, Name is 2,4-Dichloropyrido[3,4-d]pyrimidine, SMILES is ClC1=NC2=C(C=CN=C2)C(Cl)=N1, in an article , author is Xu, Xu, once mentioned of 908240-50-6, Category: pyrimidines.

Ruthenium-Catalyzed Meta-Selective C-H Difluoromethylation of Phenol Derivatives

With pyrimidine as the directing group, we achieved the meta-selective difluoromethylation of phenol derivatives using ruthenium as a catalyst. This synthetic scheme provided an efficient method for the syntheses of fluorine-containing phenol derivatives. A wide variety of phenol derivatives were well-suited, affording the corresponding products in moderate-to-good yields.

But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 908240-50-6, you can contact me at any time and look forward to more communication. Category: pyrimidines.

Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Product Details of 908240-50-6, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 908240-50-6, Name is 2,4-Dichloropyrido[3,4-d]pyrimidine, molecular formula is C7H3Cl2N3. In an article, author is Yang, Liuqing,once mentioned of 908240-50-6.

High-Performance Red Quantum-Dot Light-Emitting Diodes Based on Organic Electron Transporting Layer

High-performance red quantum dot light-emitting diodes (QLEDs) are demonstrated based on nitrogen heterocycle-containing compounds as the organic electron transporting layer (ETL). Unlike ZnO, the adoption of organic ETL can eliminate unwanted photoluminescence quenching of colloidal quantum dots (QDs) due to the prevented electron transfer between QDs and organic ETL. Most importantly, when the central core is varied from benzene and pyrimidine to triazine, their lowest unoccupied molecular orbital energy levels are found to be well tuned to facilitate electron injection. Consequently, a triazine-cored organic ETL (denoted as TmPPPyTz) achieves a restored charge balance, giving a record-high external quantum efficiency of 13.4% (18.8 cd A(-1), 23.9 lm W-1) and Commission Internationale de l’Eclairage coordinates of (0.68, 0.32). The obtained state-of-art performance clearly indicates the great potential of organic ETL towards efficient QLEDs.

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Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia

Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. , Recommanded Product: 908240-50-6, 908240-50-6, Name is 2,4-Dichloropyrido[3,4-d]pyrimidine, molecular formula is C7H3Cl2N3, belongs to pyrimidines compound. In a document, author is Abou-Elkhair, Reham A. I., introduce the new discover.

2-Hydroxyimino-6-aza-pyrimidine nucleosides: synthesis, DFT calculations, and antiviral evaluations

The global public health concerns and economic impact caused by emerging outbreaks of RNA viruses call for the search for new direct acting antiviral agents. Herein, we describe the synthesis, DFT calculations, and antiviral evaluation of a series of novel 2-hydroxyimino-6-aza-pyrimidine ribonucleosides. DFT//B3LYP/6-311+G** calculations of the tautomeric distributions of the 2-hydroxyimino nucleosides 7, 8, and 9 in aqueous environments indicate a predominance of the canonical 2-(E)-hydroxyimino structure, where the hydroxyl group points away from the sugar moiety. The conformer distributions of the latter geometrical isomers of 7, 8, and 9 support the formation of five membered rings via hydrogen bonding between the (E)-C-2 = N-O-H moiety and N-3-H of 7 and 8 and between (E)-C-2 = N-O-H and N-3 of 9, creating purine shaped nucleosides with the glycosidic linkage at the pyrimidine ring. The newly synthesized nucleosides were screened against an RNA viral panel, of which moderate antiviral activity was observed against Zika virus (ZIKV) and human respiratory syncytial virus (HRSV). 6-Aza-2-hydroxyimino-5-methyluridine derivative 18 showed activity against ZIKV (EC50 3.2 mu M), while its peracetylated derivative 19 showed activity against HRSV (EC50 5.2 mu M). The corresponding 4-thiono-2-hydroxyimino derivative 8 showed activity against HRSV (EC50 6.1 mu M) and against ZIKA (EC50 2.4 mu M). This study shows that the 6-aza-2-hydroxyimino-5-methyluracil derived nucleosides can be further optimized to provide potent antiviral agents.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 908240-50-6. Recommanded Product: 908240-50-6.

Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia

In an article, author is Shahbazi-Alavi, Hossein, once mentioned the application of 908240-50-6, Name is 2,4-Dichloropyrido[3,4-d]pyrimidine, molecular formula is C7H3Cl2N3, molecular weight is 200.0248, MDL number is MFCD10699461, category is pyrimidines. Now introduce a scientific discovery about this category, Product Details of 908240-50-6.

Co3O4/NiO@GQDs@SO3H nanocomposite as high performance catalyst for the preparation of pyrimidines

Co3O4/NiO@GQDs@SO3H nanocatalyst has been used as an effective catalyst for the preparation of 2,4-diamino-6-arylpyrimidine-5-carbonitrile derivatives through a three-component reaction of malononitrile, aromatic aldehydes and guanidine hydrochloride under reflux conditions in ethanol. The catalyst has been characterized by FT-IR, XRD, SEM, EDS, BET, TGA, XPS and VSM. Atom economy, reusable catalyst, low catalyst loading, applicability to a wide range of substrates and high yields of products are some of the notable features of this protocol.

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Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels. 908240-50-6, Name is 2,4-Dichloropyrido[3,4-d]pyrimidine, molecular formula is C7H3Cl2N3. In an article, author is Shiraiwa, Ken,once mentioned of 908240-50-6, Recommanded Product: 908240-50-6.

Effect of S-1 on blood levels of phenobarbital and phenytoin: A case report

Drug-drug interaction of fluorinated pyrimidine anticancer agents with phenytoin is well known, but interaction with phenobarbital is limited. We describe a case showing increases in plasma phenobarbital as well as phenytoin concentrations during preoperative S-1 (tegafur/gimeracil/oteracil) and radiation therapy for rectal cancer.

Interested yet? Keep reading other articles of 908240-50-6, you can contact me at any time and look forward to more communication. Recommanded Product: 908240-50-6.

Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia

Synthetic Route of 908240-50-6, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C¨CH bond functionalisation has revolutionised modern synthetic chemistry. 908240-50-6, Name is 2,4-Dichloropyrido[3,4-d]pyrimidine, SMILES is ClC1=NC2=C(C=CN=C2)C(Cl)=N1, belongs to pyrimidines compound. In a article, author is Song, Da-Wei, introduce new discover of the category.

In vitro and in vivo evaluation of antiviral activity of a phenylpropanoid derivative against spring viraemia of carp virus

Phenylpropanoids, common natural compounds, possess many different biological activities such as antioxidant, anti-inflammatory and antiviral. Spring viraemia of carp virus (SVCV) can cause a high mortality in common carp (Cyprinus carpio). However, there are currently no licenced drugs that effectively cure this disease. In this study, we designed and synthesized a phenylpropanoid derivative 4-(4-methoxyphenyl)-3,4-dihydro-2H-chromeno[4,3-d]pyrimidine-2,5(1 H)-dione (E2), and explored the antiviral effect against SVCV in vitro and in vivo. Up to 25 mg/L of E2 significantly inhibited the expression levels of SVCV protein genes in the epithelioma papulosum cyprini (EPC) cell line by a maximum inhibitory rate of >90%. As expected, E2 remarkably declined the apoptotic of SVCV-infected cells and suppressed potential enhancement of the mitochondrial membrane potential (Delta Psi m), these data implied that E2 could protect mitochondria from structural damage in response to SVCV. Meanwhile, E2 was added to EPC cells under four different conditions: time-of-addition, time-of-removal, pre-treatment of viruses and pre-treatment of cells indicated that E2 may block the post-entry transport process of the virus. Additionally, the up-regulation of six interferon (IFN)-related genes also demonstrated that E2 indirectly activated IFNs for the clearance of SVCV in common carp. Drug cure effect showed that treatment with E2 at 0.5 d post infection (dpi) is more effective than at 0, 1 or 2 dpi. Most importantly, intraperitoneal therapy of E2 markedly improved common carp survival rate and reduced virus copies in body. Therefore, the E2 has potential to be developed into a novel anti-SVCV agent.

Synthetic Route of 908240-50-6, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 908240-50-6.

Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia

Chemistry is traditionally divided into organic and inorganic chemistry. The former is the study of compounds containing at least one carbon-hydrogen bonds. 908240-50-6, Name is 2,4-Dichloropyrido[3,4-d]pyrimidine, molecular formula is C7H3Cl2N3, belongs to pyrimidines compound, is a common compound. In a patnet, author is Chiari, Laise P. A., once mentioned the new application about 908240-50-6, Recommanded Product: 2,4-Dichloropyrido[3,4-d]pyrimidine.

Drug design of new sigma-1 antagonists against neuropathic pain: A QSAR study using partial least squares and artificial neural networks

Neuropathic pain is a cureless syndrome and affects considerably the life quality of people stricken by it. Drugs currently used for its treatment do not significantly reduce the symptoms and/or have many side effects. In the search for other therapeutic approaches, the sigma-1 receptor has been pointed out as a promising drug target for the treatment of neuropathic pain. As part of our effort to help the development of new therapeutic agents against neuropathic pain, we have applied techniques of quantitative structure-activity relationships (QSAR) to a series of compounds having the pyrimidine as scaffold using Partial Least Squares (PLS) and Artificial Neural Networks (ANN) to design new sigma-1R antagonists. Next, we have calculated a plethora of descriptors, which were selected from correlation matrix and genetic algorithm (AG). The selected descriptors were used to construct PLS and ANN models and, from them, various results were used to design new antagonists. At last, the designed compounds were subjected to the our QSAR models to predict their biological activity values. The new compounds exhibited significant biological affinity values, and among them we can highlight the compounds L2, L4, L14, L17, and L18 with excellent predicted pK i values confirmed by both PLS and ANN models. Therefore, the predictive ability of the PLS and ANN models here presented and their robustness allowed to extract important information that can be used in the design of new compounds as well as to predict their biological activity values. (C) 2020 Published by Elsevier B.V.

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, 908240-50-6. The above is the message from the blog manager. Recommanded Product: 2,4-Dichloropyrido[3,4-d]pyrimidine.

Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia

Chemistry is traditionally divided into organic and inorganic chemistry. The former is the study of compounds containing at least one carbon-hydrogen bonds. 908240-50-6, Name is 2,4-Dichloropyrido[3,4-d]pyrimidine, molecular formula is C7H3Cl2N3, belongs to pyrimidines compound, is a common compound. In a patnet, author is de Souza, Cesar A. S., once mentioned the new application about 908240-50-6, Product Details of 908240-50-6.

ASARONE-DERIVED PHENYLPROPANOIDS AND ISOQUINOLINE-DERIVED ALKALOIDS FROM THE BARK OF Duguetia pycnastera (Annonaceae) AND THEIR CYTOTOXICITIES

The phytochemical investigation of the hexane and methanol extracts from the bark of Duguetia pycnastera Sandwith (Annonaceae) afforded seven known compounds, two asarone-derived phenylpropanoids and five isoquinoline-derived alkaloids. The asarones, gamma-asarone (1-allyl-2,4,5-trimethoxybenzene) and 2,4,5-trimethoxy-styrene were isolated of the hexane extract while the aporphine alkaloids, O-methylmoschatoline, lysicamine, nornuciferidine, and guatterine N-oxide, and the benzyltetrahydroisoquinoline alkaloid, (S)-reticuline were isolated of the alkaloid fraction of the methanol extract. This is the first report of these compounds in D. pycnastera. gamma-Asarone is being reported for the first time in the Annonaceae. Nornuciferidine is described for the second time in the Annonaceae while guatterine N-oxide is the third register. The structures of the isolated compounds were established by extensive analyses using 1D and 2D NMR spectroscopy in combination with MS. The cytotoxic activity of the isolated compounds (except for nornuciferidine) was evaluated against cancer and non-cancerous cell lines, in which lysicamine was the most active compound, mainly against HL-60, HepG2, and K562 with IC50 values of 24.40, 28.86 and 38.75 mu mol L-1, respectively.

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, 908240-50-6. The above is the message from the blog manager. Product Details of 908240-50-6.

Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia