Cas 927691-95-0,Pentanethioic acid, 5-amino-5-oxo-2-[[(phenylmethoxy)carbonyl]amino]-, S-[2-(acetylamino)ethyl] ester, (2S)-

927691-95-0

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Basic information

Product Name: Pentanethioic acid, 5-amino-5-oxo-2-[[(phenylmethoxy)carbonyl]amino]-, S-[2-(acetylamino)ethyl] ester, (2S)-
Synonyms:
CAS NO:927691-95-0
Molecular Formula: C17H23N3O5S
Molecular Weight: 381.453
EINECS: N/A
Product Categories: N/A
Mol File: 927691-95-0.mol
Article Data: 1

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: Pentanethioic acid, 5-amino-5-oxo-2-[[(phenylmethoxy)carbonyl]amino]-, S-[2-(acetylamino)ethyl] ester, (2S)-(CAS DataBase Reference)
NIST Chemistry Reference: Pentanethioic acid, 5-amino-5-oxo-2-[[(phenylmethoxy)carbonyl]amino]-, S-[2-(acetylamino)ethyl] ester, (2S)-(927691-95-0)
EPA Substance Registry System: Pentanethioic acid, 5-amino-5-oxo-2-[[(phenylmethoxy)carbonyl]amino]-, S-[2-(acetylamino)ethyl] ester, (2S)-(927691-95-0)

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: 927691-95-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 927691-95-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,7,6,9 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 927691-95:
(8*9)+(7*2)+(6*7)+(5*6)+(4*9)+(3*1)+(2*9)+(1*5)=220
220 % 10 = 0
So 927691-95-0 is a valid CAS Registry Number.

927691-95-0Upstream product

132388-60-4 (S)-2-(((benzyloxy)carbonyl)amino)-5-oxo-5-(tritylamino)pentanoic acid

927691-95-0Downstream Products

927691-95-0Relevant articles and documents

Biomimetic catalysis of intermodular aminoacyl transfer

Wilcoxen, Keith M.,Leman, Luke J.,Weinberger, Dana A.,Huang, Zheng-Zheng,Ghadiri, M. Reza

, p. 748 - 749 (2007/10/03)

Intermodular aminoacyl transfer is the fundamental bond-forming reaction in the biosynthesis of polypeptides by ribosomes and nonribosomal peptide synthetases (NRPS). Here we report the design and functional characterizations of short synthetic α-helical

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