Cas 951132-65-3,2-chloro-N-(5-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-4-methyl-thiazol-2-yl)-benzamide

951132-65-3

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Basic information

Product Name: 2-chloro-N-(5-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-4-methyl-thiazol-2-yl)-benzamide
Synonyms: 2-chloro-N-(5-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-4-methyl-thiazol-2-yl)-benzamide
CAS NO:951132-65-3
Molecular Formula:
Molecular Weight: 402.748
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-chloro-N-(5-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-4-methyl-thiazol-2-yl)-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-chloro-N-(5-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-4-methyl-thiazol-2-yl)-benzamide(951132-65-3)
EPA Substance Registry System: 2-chloro-N-(5-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-4-methyl-thiazol-2-yl)-benzamide(951132-65-3)

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: 951132-65-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 951132-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,1,3 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 951132-65:
(8*9)+(7*5)+(6*1)+(5*1)+(4*3)+(3*2)+(2*6)+(1*5)=153
153 % 10 = 3
So 951132-65-3 is a valid CAS Registry Number.

951132-65-3Upstream product

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951132-65-3Relevant academic research and scientific papers

Synthesis and photosynthetic inhibition activity of substituted 5-(bis-trifluoromethyl)methyl)-2-aminothiazoles

Boyer, Cécile,Finazzi, Giovanni,Laurent, Philippe,Haas, Alois,Blancou, Hubert

, p. 1522 - 1527 (2006)

The reaction of 5,5,5-trifluoro-4-trifluoromethyl-pent-3-en-2-one with aminothiocarbonyls yielded aminothiourea precursors which readily cyclised to the corresponding thiazole derivatives, 5-(bis-trifluoromethyl)methyl)-2-aminothiazoles. The inhibitory po

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