Cas 876322-97-3,Carbamic acid, [(1S)-2-oxo-1-(phenylmethyl)-2-[[1-(phenylsulfonyl)propyl]amino]ethyl]-, phenylmethyl ester

876322-97-3

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Basic information

Product Name: Carbamic acid, [(1S)-2-oxo-1-(phenylmethyl)-2-[[1-(phenylsulfonyl)propyl]amino]ethyl]-, phenylmethyl ester
Synonyms:
CAS NO:876322-97-3
Molecular Formula: C26H28N2O5S
Molecular Weight: 480.585
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: Carbamic acid, [(1S)-2-oxo-1-(phenylmethyl)-2-[[1-(phenylsulfonyl)propyl]amino]ethyl]-, phenylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [(1S)-2-oxo-1-(phenylmethyl)-2-[[1-(phenylsulfonyl)propyl]amino]ethyl]-, phenylmethyl ester(876322-97-3)
EPA Substance Registry System: Carbamic acid, [(1S)-2-oxo-1-(phenylmethyl)-2-[[1-(phenylsulfonyl)propyl]amino]ethyl]-, phenylmethyl ester(876322-97-3)

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: 876322-97-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 876322-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,3,2 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 876322-97:
(8*8)+(7*7)+(6*6)+(5*3)+(4*2)+(3*2)+(2*9)+(1*7)=203
203 % 10 = 3
So 876322-97-3 is a valid CAS Registry Number.

876322-97-3Upstream product

876322-97-3Downstream Products

876322-97-3Relevant academic research and scientific papers

α-Amido sulfones from natural α-amino acids and their reaction with carbon nucleophiles

Petrini, Marino,Seri, Mirko

, p. 960 - 967 (2006)

Amides obtained from N-carbamoyl α-amino acids react with aldehydes in the presence of benzenesulfinic acid to give α-amido sulfones in good yield. These derivatives act as equivalents of N-acylimines in the reaction with nucleophiles leading to the corre

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