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136547-20-1

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136547-20-1 Usage

General Description

4-trifluoromethyl-2-methylthio-pyrimidine is a specific chemical compound derived from pyrimidine, a heterocyclic organic molecule. It is characterized by the presence of a trifluoromethyl group and a methylthio group, which are both important for its chemical and biological properties. 4-trifluoromethyl-2-methylthio-pyrimidine has shown potential in various applications, including pharmaceuticals and agrochemicals. It may exhibit biological activity, such as as an antiviral or antibacterial agent, due to its structural features. Additionally, 4-trifluoromethyl-2-methylthio-pyrimidine may serve as a precursor or intermediate in the synthesis of more complex organic compounds for further research and development purposes. Despite its potential benefits, the chemical should be handled and used with caution due to its potential hazards and risks.

Check Digit Verification of cas no

The CAS Registry Mumber 136547-20-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,5,4 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 136547-20:
(8*1)+(7*3)+(6*6)+(5*5)+(4*4)+(3*7)+(2*2)+(1*0)=131
131 % 10 = 1
So 136547-20-1 is a valid CAS Registry Number.

136547-20-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylsulfanyl-4-(trifluoromethyl)pyrimidine

1.2 Other means of identification

Product number -
Other names 4-trifluoromethyl-2-methylthiopyrimidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:136547-20-1 SDS

136547-20-1Relevant articles and documents

Triphenylethanamine Derivatives as Cholesteryl Ester Transfer Protein Inhibitors: Discovery of N-[(1R)-1-(3-Cyclopropoxy-4-fluorophenyl)-1-[3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)phenyl]-2-phenylethyl]-4-fluoro-3-(trifluoromethyl)benzamide (BMS-795311)

Qiao, Jennifer X.,Wang, Tammy C.,Adam, Leonard P.,Chen, Alice Ye A.,Taylor, David S.,Yang, Richard Z.,Zhuang, Shaobin,Sleph, Paul G.,Li, Julia P.,Li, Danshi,Yin, Xiaohong,Chang, Ming,Chen, Xue-Qing,Shen, Hong,Li, Jianqing,Smith, Daniel,Wu, Dauh-Rurng,Leith, Leslie,Harikrishnan, Lalgudi S.,Kamau, Muthoni G.,Miller, Michael M.,Bilder, Donna,Rampulla, Richard,Li, Yi-Xin,Xu, Carrie,Lawrence, R. Michael,Poss, Michael A.,Levesque, Paul,Gordon, David A.,Huang, Christine S.,Finlay, Heather J.,Wexler, Ruth R.,Salvati, Mark E.

, p. 9010 - 9026 (2015)

Cholesteryl ester transfer protein (CETP) inhibitors raise HDL-C in animals and humans and may be antiatherosclerotic by enhancing reverse cholesterol transport (RCT). In this article, we describe the lead optimization efforts resulting in the discovery o

Haloacetylated Enol Ethers: 4. Synthesis of 4-Trihalomethyl-2-methylthiopyrimidines

Madruga, Claudia da C.,Clerici, Edflia,Martins, Marcos A. P.,Zanatta, Nilo

, p. 735 - 738 (2007/10/02)

The synthesis of a series of 5- and 6-substituted 4-trihalomethyl-2-methylthiopyrimidines, prepared from the cyclocondensation reaction of β-alkoxyvinyl trichloromethyl ketones with 2-methyl-2-thiopseudourea sulfate, are reported.A systematic study to find the best reation conditions werre carried out.

4-TRIFLUOROMETHYLPYRIMIDINES

Gerus, I. I.,Vdovenko, S. I.,Gorbunova, M. G.,Kukhar', V. P.

, p. 398 - 406 (2007/10/02)

It is shown that β-alkoxyvinyl trifluoromethyl ketones are convenient reagents for the synthesis of 4-trifluoromethylpyrimidines that contain a hydrogen atom or hydroxy, mercapto, and amino groups in the 2 position.The NMR, IR, and UV spectra of the synth

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