Cas 329901-76-0,(R)-N-[2-chloro-3-methyl-4-(chlorosulphonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide

329901-76-0

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Basic information

Product Name: (R)-N-[2-chloro-3-methyl-4-(chlorosulphonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide
Synonyms: (R)-N-[2-chloro-3-methyl-4-(chlorosulphonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide
CAS NO:329901-76-0
Molecular Formula:
Molecular Weight: 380.172
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: (R)-N-[2-chloro-3-methyl-4-(chlorosulphonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide(CAS DataBase Reference)
NIST Chemistry Reference: (R)-N-[2-chloro-3-methyl-4-(chlorosulphonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide(329901-76-0)
EPA Substance Registry System: (R)-N-[2-chloro-3-methyl-4-(chlorosulphonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-methylpropanamide(329901-76-0)

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: 329901-76-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 329901-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,9,0 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 329901-76:
(8*3)+(7*2)+(6*9)+(5*9)+(4*0)+(3*1)+(2*7)+(1*6)=160
160 % 10 = 0
So 329901-76-0 is a valid CAS Registry Number.

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329901-76-0Relevant academic research and scientific papers

Chemical compounds

-

, (2008/06/13)

A compound of formula (I) wherein: R1, R2, R3, R4, R5, R6and R7are as defined within; or a pharmaceutically acceptable salt or an in vivo hydrolysable ester thereof is described. The use of compounds of formula (I) in the production of an elevation of PDH activity in a warm-blooded animal such as a human being are also described. Pharmaceutical compositions, methods and processes for preparation of compounds of formula (I) are detailed.

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