Category: 4318-56-3

Chemistry, like all the natural sciences, SDS of cas: 4318-56-3, begins with the direct observation of nature¡ª in this case, of matter.4318-56-3, Name is 6-Chloro-3-methylpyrimidine-2,4(1H,3H)-dione, SMILES is O=C1N(C)C(C=C(Cl)N1)=O, belongs to pyrimidines compound. In a document, author is Da Silva, Andreia M. P. W., introduce the new discover.

Design, Synthesis, and Cholinesterase Inhibitory Activity of 4-Substituted-6-(trihalomethyl)-2-methylsulfanyl Pyrimidines

A chemoselective approach is reported for the synthesis of 4-(bromo/chloro)methyl-2-methylsulfanyl-6-trihalomethyl pyrimidines and subsequent nucleophilic substitution of the halomethyl moiety with aminoalcohols. The final compounds were choline derivatives (bearing a pyrimidine ring). These were tested as AChE and BChE inhibitors, and presented IC50 values in the range of 13.8-81.6 mu M. Remarkably, the trichloromethyl pyrimidines were the most active compounds. Docking studies and ADMET properties are also reported.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 4318-56-3. SDS of cas: 4318-56-3.

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

Synthetic Route of 4318-56-3, Chemo-enzymatic cascade processes are invaluable due to their ability to rapidly construct high-value products from available feedstock chemicals in a one-pot relay manner. 4318-56-3, Name is 6-Chloro-3-methylpyrimidine-2,4(1H,3H)-dione, SMILES is O=C1N(C)C(C=C(Cl)N1)=O, belongs to pyrimidines compound. In a article, author is Park, Jun Hyung, introduce new discover of the category.

Synthesis of a DNA-Encoded Library of Pyrrolo[2,3-d]pyrimidines

Developing DNA-encoded libraries of privileged scaffolds, such as pyrrolopyrimidines, is of great interest in drug discovery and chemical biology as a powerful tool to rapidly and inexpensively discover potent drug candidates. However, it is often challenging to construct such DNA-encoded libraries because many reaction conditions are not compatible with DNA. Here, we describe the development of a convenient solid-phase synthetic strategy that overcomes the current limitations and allows the efficient synthesis of a DNA-encoded combinatorial library of structurally diverse tetra-substituted pyrrolo[2,3-d]pyrimidines.

Synthetic Route of 4318-56-3, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 4318-56-3.

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

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 4318-56-3, Name is 6-Chloro-3-methylpyrimidine-2,4(1H,3H)-dione, SMILES is O=C1N(C)C(C=C(Cl)N1)=O, in an article , author is El Faydy, M., once mentioned of 4318-56-3, Product Details of 4318-56-3.

An experimental-coupled empirical investigation on the corrosion inhibitory action of 7-alkyl-8-Hydroxyquinolines on C35E steel in HCl electrolyte

Two 8-Hydroxyquinoline-based piperazine, 7-((4-(4-chloro phenyl)piperazin-1-yl) methyl) quinolin-8-ol (CPQ) and 7-((4-methyl piperazin-1-yl) methyl)quinolin-8-ol (MPQ) were prepared, identified and investigated as corrosion inhibiting additives of C35E steel in HCl electrolyte using experimental and theoretical tools. All outcomes findings confirm that CPQ and MPQ significantly improved anti-corrosion properties of C35E steel and CPQ performed better than MPQ and their inhibition efficiency depends on the temperature, the amount, and the chemical structure of the inhibitor. The eta(max) of CPQ and MPQ reaches as much as 91.5% and 86.3% at 10(-3) M, respectively. EIS outcomes revealed that the corrosion of C35E steel is controlled by only one charge transfer mechanism and the adsorbed CPQ and MPQ molecules decreased the steel dissolution by developing a pseudo-capacitive film on the steel surface. Both additives revealed mixed-type inhibitory activity, lowering of cathodic and anodic corrosion reactions rate, as proposed from the polarization investigation. The UV-Visible spectra suggest the existence of strong interaction between iron cations and 7-(4-alkylpiperazinylmethyl)-8-Hydroxyquinolines molecules. The 7-(4-alkylpiperazinylmethyl)-8-Hydroxyquinolines were chemisorbed on the C35E steel surface in accordance with Langmuir adsorption isotherm. Temperature influence studies of CPQ and MPQ adsorption behavior, as well as estimated thermodynamic magnitudes, are consistent with a physisorption process. The computational correlations (DFT, Monte Carlo, and Molecular Dynamic simulations) justify the experimental observations. (C) 2020 Elsevier B.V. All rights reserved.

Interested yet? Read on for other articles about 4318-56-3, you can contact me at any time and look forward to more communication. Product Details of 4318-56-3.

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

Synthetic Route of 4318-56-3, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 4318-56-3, name is 6-Chloro-3-methylpyrimidine-2,4(1H,3H)-dione. This compound has unique chemical properties. The synthetic route is as follows.

7.71 g of 2-cyanobenzyl bromide (R1 is H and R2 is Br), 6.00 g of 3-methyl-6-chlorouracil and 4.20 g of triethylamine were dissolved in a mixed solution of 78 ml of DMSO and THF, and the temperature was raised The reaction was stirred at 50 C for 1 h, and the reaction was cooled to room temperature. 80 ml of ice water was slowly added dropwise, and the mixture was stirred for 1 h under ice-cooling. The crude product of compound III was 9.15 g. The yield was 88.81%. The crude compound III was rinsed with ethyl acetate at 25 C, filtered, washed and dried to give pure Compound III 8.94. The purification yield was 97.90%. The total yield of compound was 86.77% and the purity was 89.70%.

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 4318-56-3, 6-Chloro-3-methylpyrimidine-2,4(1H,3H)-dione.

Reference:
Patent; Beijing Wansheng Pharmaceutical Co., Ltd.; Lin Guoliang; Wang Qiang; Jiang Yugang; Wang Yiping; Kang Yi; Lv Xiaona; (10 pag.)CN106608853; (2017); A;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia

Reference of 4318-56-3, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 4318-56-3, name is 6-Chloro-3-methylpyrimidine-2,4(1H,3H)-dione. This compound has unique chemical properties. The synthetic route is as follows.

Step 1 : 6-Chloro-3-methylpyrimidine-2,4 (l/7,3/7)-dione (43 g, 267 mmol), (1192) K2C03 (92.1 g, 667 mmol) and PMB-C1 (1.4 g, 28.0 mmol) were taken up in DMF (500 mL). The reaction mixture was stirred at 50 C for 16 hours. The mixture was partitioned between H20 (1000 mL) and EtOAc (1500 mL) and the aqueous phase was extracted with EtOAc (800 mL x 2). The combined organics were washed with brine (500 mL x 2), dried over anhydrous Na2S04, filtered, and concentrated under reduced pressure to give a residue.Trituration with petroleum ether/EtOAc (10 : 1) resulted in the formation of a precipitate which was collected by filtration, washed with petroleum ether/EtOAc (10 : l, 100 mL), and dried to give 6-chloro-l-(4-methoxybenzyl)-3-methylpyrimidine-2, 4(1/7, 3/7)-dione (50.0 g, 66.7% yield) as a white solid.

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 4318-56-3, 6-Chloro-3-methylpyrimidine-2,4(1H,3H)-dione.

Reference:
Patent; RELAY THERAPEUTICS, INC.; D.E. SHAW RESEARCH, LLC; WALTERS, W., Patrick; LESCARBEAU, Andre; KELLEY, Elizabeth, H.; SHORTSLEEVES, Kelley, C.; TAYLOR, Alexander, M.; PIERCE, Levi Charles, Thomas; MURCKO, Mark, Andrew; GIORDANETTO, Fabrizio; GREISMAN, Jack, Benjamin; MARAGAKIS, Paul; BHAT, Sathesh; KONZE, Kyle; DAHLGREN, Markus, Kristofer; THERRIEN, Eric; (0 pag.)WO2019/165073; (2019); A1;,
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia