Cas 1270152-52-7,N-(((S)-2-(ethylthio)-4-isopropyl-5-oxo-4,5-dihydrothiazol-4-yl)(phenyl)methyl)-4-methylbenzenesulfonamide

1270152-52-7

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Basic information

Product Name: N-(((S)-2-(ethylthio)-4-isopropyl-5-oxo-4,5-dihydrothiazol-4-yl)(phenyl)methyl)-4-methylbenzenesulfonamide
Synonyms:
CAS NO:1270152-52-7
Molecular Formula:
Molecular Weight: 462.658
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: N-(((S)-2-(ethylthio)-4-isopropyl-5-oxo-4,5-dihydrothiazol-4-yl)(phenyl)methyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(((S)-2-(ethylthio)-4-isopropyl-5-oxo-4,5-dihydrothiazol-4-yl)(phenyl)methyl)-4-methylbenzenesulfonamide(1270152-52-7)
EPA Substance Registry System: N-(((S)-2-(ethylthio)-4-isopropyl-5-oxo-4,5-dihydrothiazol-4-yl)(phenyl)methyl)-4-methylbenzenesulfonamide(1270152-52-7)

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: 1270152-52-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1270152-52-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,0,1,5 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1270152-52:
(9*1)+(8*2)+(7*7)+(6*0)+(5*1)+(4*5)+(3*2)+(2*5)+(1*2)=117
117 % 10 = 7
So 1270152-52-7 is a valid CAS Registry Number.

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1270152-52-7Relevant academic research and scientific papers

Asymmetric aza-Mannich addition: Synthesis of modified chiral 2-(ethylthio)-thiazolone derivatives with anticancer potency

Liu, Xiaodong,Deng, Leijiao,Song, Hongjin,Jia, Huazhen,Wang, Rui

, p. 1494 - 1497 (2011)

An easily prepared cinchona alkaloid derivative was found to be an effective organocatalyst in a direct, enantioselective aza-Mannich addition. By establishing a quaternary carbon stereocenter, a series of modified chiral 2-(ethylthio)-thiazolone derivati

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