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16097-63-5

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16097-63-5 Usage

Chemical Properties

Colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 16097-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,9 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16097-63:
(7*1)+(6*6)+(5*0)+(4*9)+(3*7)+(2*6)+(1*3)=115
115 % 10 = 5
So 16097-63-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H4ClF3N2S/c1-13-5-11-3(6(8,9)10)2-4(7)12-5/h2H,1H3

16097-63-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H61620)  4-Chloro-2-methylthio-6-(trifluoromethyl)pyrimidine, 97%   

  • 16097-63-5

  • 1g

  • 743.0CNY

  • Detail
  • Alfa Aesar

  • (H61620)  4-Chloro-2-methylthio-6-(trifluoromethyl)pyrimidine, 97%   

  • 16097-63-5

  • 5g

  • 2975.0CNY

  • Detail

16097-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-2-(Methylsulfanyl)-6-(Trifluoromethyl)Pyrimidine

1.2 Other means of identification

Product number -
Other names 4-chloro-2-methylsulfanyl-6-(trifluoromethyl)pyrimidine

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:16097-63-5 SDS

16097-63-5Relevant articles and documents

PYRIMIDINE AND FIVE-MEMBERED NITROGEN HETEROCYCLE DERIVATIVE, PREPARATION METHOD THEREFOR, AND MEDICAL USES THEREOF

-

Paragraph 0140; 0141, (2021/10/07)

The present invention relates to a pyrimidine and a five-membered nitrogen heterocycle derivative, a preparation method therefor, and the medical uses thereof. Particularly, the present invention relates to a pyrimidine and a five-membered nitrogen hetero

Discovery of Highly Potent 2-Sulfonyl-Pyrimidinyl Derivatives for Apoptosis Inhibition and Ischemia Treatment

Li, Li,Jiang, Xian,Huang, Shaoqiang,Ying, Zhengxin,Zhang, Zhaolan,Pan, Chenjie,Li, Sisi,Wang, Xiaodong,Zhang, Zhiyuan

supporting information, p. 407 - 412 (2017/04/21)

A series of 2-sulfonyl-pyrimidinyl derivatives was developed as apoptosis inhibitors. These represent the first class of apoptosis inhibitors that function through stabilizing mitochondrial respiratory complex II. Starting from a phenotypic screen hit with micromolar activity, we optimized the cellular apoptosis inhibition activity of 2-sulfonyl-pyrimidinyl derivatives to picomolar level (compound 42, also named as TC9-305). The therapeutic potential of these new apoptosis inhibitors was further demonstrated by their neuroprotective effect on an ischemic animal model.

Synthesis and Metalation of Trifluoromethylpyrimidines. Metalation of Diazines. XVI

Ple, N.,Turck, A.,Heynderickx, A.,Queguiner, G.

, p. 551 - 556 (2007/10/03)

A new route to trifluoromethylpyrimidines is described.Lithiation of trifluoromethylpyrimidines was successfully achieved and was used to synthesize new pyrimidine derivatives.A new synthetic route to a biologically active molecule with antimycotic activi

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