Cas 146548-60-9,[(S)-5-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-5-(2,4,6-trimethoxy-benzylcarbamoyl)-pentyl]-carbamic acid benzyl ester

146548-60-9

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Basic information

Product Name: [(S)-5-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-5-(2,4,6-trimethoxy-benzylcarbamoyl)-pentyl]-carbamic acid benzyl ester
Synonyms:
CAS NO:146548-60-9
Molecular Formula:
Molecular Weight: 706.836
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: [(S)-5-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-5-(2,4,6-trimethoxy-benzylcarbamoyl)-pentyl]-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-5-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-5-(2,4,6-trimethoxy-benzylcarbamoyl)-pentyl]-carbamic acid benzyl ester(146548-60-9)
EPA Substance Registry System: [(S)-5-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-5-(2,4,6-trimethoxy-benzylcarbamoyl)-pentyl]-carbamic acid benzyl ester(146548-60-9)

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: 146548-60-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 146548-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,5,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 146548-60:
(8*1)+(7*4)+(6*6)+(5*5)+(4*4)+(3*8)+(2*6)+(1*0)=149
149 % 10 = 9
So 146548-60-9 is a valid CAS Registry Number.

146548-60-9Upstream product

146548-60-9Downstream Products

146548-60-9Relevant academic research and scientific papers

Novel Chemoenzymatic Synthesis of Peptide C-Terminal Amides from Ester Precursors

Green, Jeremy,Margolin, Alexey L.

, p. 7759 - 7760 (1992)

A novel two step chemoenzymatic procedure for the preparation of peptide C-terminal amides has been developed.

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