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1-[4-(4-CHLOROPHENYL)-1,3-THIAZOL-2-YL]-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

159885-82-2

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159885-82-2 Usage

Chemical class

Pyrazole carboxylic acids

Molecular structure

Contains a thiazole ring, a chlorophenyl group, and a trifluoromethyl group

Pharmacological activity

Potential due to the presence of a carboxylic acid moiety

Chemical interactions

Can participate in various interactions with biological molecules

Further research

Specific properties and potential applications may be studied in the fields of chemistry and pharmaceuticals

Check Digit Verification of cas no

The CAS Registry Mumber 159885-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,8,8 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 159885-82:
(8*1)+(7*5)+(6*9)+(5*8)+(4*8)+(3*5)+(2*8)+(1*2)=202
202 % 10 = 2
So 159885-82-2 is a valid CAS Registry Number.

159885-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-(4-chlorophenyl)-1,3-thiazol-2-yl]-5-(trifluoromethyl)pyrazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names HMS2864G19

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:159885-82-2 SDS

159885-82-2Downstream Products

159885-82-2Relevant academic research and scientific papers

Novel thiazole-based heterocycles as selective inhibitors of fibrinogen- mediated platelet aggregation

Sanfilippo,Urbanski,Beers,Eckardt,Falotico,Ginsberg,Offord,Press,Tighe,Tomko,Andrade-Gordon

, p. 34 - 41 (2007/10/02)

The synthesis and biological activity of novel thiazole-based heterocycles as inhibitors of thrombin-induced human platelet aggregation are described. Further evaluation of selected compounds show they inhibit platelet aggregation as stimulated by a varie

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