Cas 78452-50-3,(S)-2-(4-Methoxy-benzyloxycarbonylamino)-4-methylsulfanyl-butyric acid methyl ester

78452-50-3

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Basic information

Product Name: (S)-2-(4-Methoxy-benzyloxycarbonylamino)-4-methylsulfanyl-butyric acid methyl ester
Synonyms: (S)-2-(4-Methoxy-benzyloxycarbonylamino)-4-methylsulfanyl-butyric acid methyl ester
CAS NO:78452-50-3
Molecular Formula:
Molecular Weight: 327.401
EINECS: N/A
Product Categories: N/A
Mol File: 78452-50-3.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: (S)-2-(4-Methoxy-benzyloxycarbonylamino)-4-methylsulfanyl-butyric acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-(4-Methoxy-benzyloxycarbonylamino)-4-methylsulfanyl-butyric acid methyl ester(78452-50-3)
EPA Substance Registry System: (S)-2-(4-Methoxy-benzyloxycarbonylamino)-4-methylsulfanyl-butyric acid methyl ester(78452-50-3)

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: 78452-50-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78452-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,5 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78452-50:
(7*7)+(6*8)+(5*4)+(4*5)+(3*2)+(2*5)+(1*0)=153
153 % 10 = 3
So 78452-50-3 is a valid CAS Registry Number.

78452-50-3Upstream product

78452-50-3Downstream Products

78452-51-4 Z(OMe)-Met-ol

78452-50-3Relevant articles and documents

CONVENIENT PROCEDURE FOR THE PREPARATION OF α-AMINO ALCOHOLS

Kubota, Minoru,Nagase, Osamu,Yajima, Haruaki

, p. 1169 - 1171 (2007/10/02)

Various Nα-protected amino acid active esters used in peptide chemistry were found to be excellent source materials for the preparation of the coresponding amino alcohols by reduction with sodium borohydride.The validity of this procedure for the convenient preparation of aliphatic alcohols was demonstrated by taking stearyl alcohol as an example.Keywords: sodium borohydride reduction; Nα-protected L-amino alcohols; Nα-protected amino acid ative esters; stearyl alcohol; stearic acid

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