Cas 321848-16-2,1-[4-(4-METHOXYPHENYL)-1,3-THIAZOL-2-YL]-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID

321848-16-2

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Basic information

Product Name: 1-[4-(4-METHOXYPHENYL)-1,3-THIAZOL-2-YL]-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID
Synonyms: 1-[4-(4-METHOXYPHENYL)-1,3-THIAZOL-2-YL]-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID
CAS NO:321848-16-2
Molecular Formula: C15H10F3N3O3S
Molecular Weight: 369.32
EINECS: N/A
Product Categories: N/A
Mol File: 321848-16-2.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-[4-(4-METHOXYPHENYL)-1,3-THIAZOL-2-YL]-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID(CAS DataBase Reference)
NIST Chemistry Reference: 1-[4-(4-METHOXYPHENYL)-1,3-THIAZOL-2-YL]-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID(321848-16-2)
EPA Substance Registry System: 1-[4-(4-METHOXYPHENYL)-1,3-THIAZOL-2-YL]-5-(TRIFLUOROMETHYL)-1H-PYRAZOLE-4-CARBOXYLIC ACID(321848-16-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 321848-16-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 321848-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,8,4 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 321848-16:
(8*3)+(7*2)+(6*1)+(5*8)+(4*4)+(3*8)+(2*1)+(1*6)=132
132 % 10 = 2
So 321848-16-2 is a valid CAS Registry Number.

321848-16-2Upstream product

159885-66-2 1-[4-(4-Methoxy-phenyl)-thiazol-2-yl]-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid ethyl ester

321848-16-2Downstream Products

321848-16-2Relevant 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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