Cas 1366127-32-3,benzyl [(2S)-1-amino-1-oxo-4-phenylbutan-2-yl]carbamate

1366127-32-3

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Basic information

Product Name: benzyl [(2S)-1-amino-1-oxo-4-phenylbutan-2-yl]carbamate
Synonyms: benzyl [(2S)-1-amino-1-oxo-4-phenylbutan-2-yl]carbamate
CAS NO:1366127-32-3
Molecular Formula:
Molecular Weight: 312.368
EINECS: N/A
Product Categories: N/A
Mol File: 1366127-32-3.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: benzyl [(2S)-1-amino-1-oxo-4-phenylbutan-2-yl]carbamate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl [(2S)-1-amino-1-oxo-4-phenylbutan-2-yl]carbamate(1366127-32-3)
EPA Substance Registry System: benzyl [(2S)-1-amino-1-oxo-4-phenylbutan-2-yl]carbamate(1366127-32-3)

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: 1366127-32-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1366127-32-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,6,1,2 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1366127-32:
(9*1)+(8*3)+(7*6)+(6*6)+(5*1)+(4*2)+(3*7)+(2*3)+(1*2)=153
153 % 10 = 3
So 1366127-32-3 is a valid CAS Registry Number.

1366127-32-3Upstream product

83793-44-6 Z-homophenylalanine

1366127-32-3Downstream Products

1366127-32-3Relevant articles and documents

Predicting and improving the membrane permeability of peptidic small molecules

Rafi, Salma B.,Hearn, Brian R.,Vedantham, Punitha,Jacobson, Matthew P.,Renslo, Adam R.

experimental part, p. 3163 - 3169 (2012/06/18)

We evaluate experimentally and computationally the membrane permeability of matched sets of peptidic small molecules bearing natural or bioisosteric unnatural amino acids. We find that the intentional introduction of hydrogen bond acceptor-donor pairs in

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