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Ethyl 2-(methylsulfanyl)-4-{[3-(trifluoromethyl)phenyl]amino}pyrimidine-5-carboxylate is a complex organic compound with the molecular formula C15H15F3N4O2S. It is characterized by a pyrimidine core, which is a heterocyclic aromatic organic compound consisting of a six-membered ring with four carbon atoms and two nitrogen atoms. The compound features a methylsulfanyl group (CH3S) at the 2-position, an amino group attached to a trifluoromethylphenyl group at the 4-position, and a carboxylate group at the 5-position. The trifluoromethylphenyl group (C6H4CF3) is a phenyl ring with three fluorine atoms attached to one of the carbon atoms. This chemical is likely to be used in pharmaceutical or chemical research due to its unique structure and potential reactivity, but its specific applications or properties are not detailed in the provided information.

3859-55-0

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3859-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3859-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,5 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3859-55:
(6*3)+(5*8)+(4*5)+(3*9)+(2*5)+(1*5)=120
120 % 10 = 0
So 3859-55-0 is a valid CAS Registry Number.

3859-55-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-methylsulfanyl-4-[3-(trifluoromethyl)anilino]pyrimidine-5-carboxylate

1.2 Other means of identification

Product number -
Other names 4-(3-Trifluormethyl-anilino)-2-methylmercapto-5-ethoxycarbonyl-pyrimidin

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:3859-55-0 SDS

3859-55-0Relevant academic research and scientific papers

Synthetic studies on novel Syk inhibitors. Part 1: Synthesis and structure-activity relationships of pyrimidine-5-carboxamide derivatives

Hisamichi, Hiroyuki,Naito, Ryo,Toyoshima, Akira,Kawano, Noriyuki,Ichikawa, Atsushi,Orita, Akiko,Orita, Masaya,Hamada, Noritaka,Takeuchi, Makoto,Ohta, Mitsuaki,Tsukamoto, Shin-Ichi

, p. 4936 - 4951 (2007/10/03)

Spleen tyrosine kinase (Syk) is a non-receptor-type tyrosine kinase which mediates diverse responses in haematopoietic cells. Therefore, Syk is an attractive therapeutic target, and in a study of Syk inhibitors as potentially new therapeutic agents, we di

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