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159885-80-0

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159885-80-0 Usage

General Description

1-(4-Phenyl-thiazol-2-yl)-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid is a complex organic compound which consists of a fusion of three distinct chemical structures: pyrazole, thiazole and a phenyl ring. The compound has a carboxylic acid group which tends to make it acidic in nature. As an organic compound with a fluorine atom, it exhibits the property of trifluoromethyl. It is designed in the laboratories and used primarily in research. Information about its exact application in a specific industry or research area is sparse, however, such complex organic molecules are commonly explored in drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 159885-80-0 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 159885-80:
(8*1)+(7*5)+(6*9)+(5*8)+(4*8)+(3*5)+(2*8)+(1*0)=200
200 % 10 = 0
So 159885-80-0 is a valid CAS Registry Number.

159885-80-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 1-(4-phenyl-1,3-thiazol-2-yl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid

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:159885-80-0 SDS

159885-80-0Downstream Products

159885-80-0Relevant articles and documents

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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