Cas 113247-53-3,(S)-1-[(S)-2-((S)-3-tert-Butoxycarbonylamino-2-hydroxy-2-methyl-4-phenyl-butylamino)-propionyl]-pyrrolidine-2-carboxylic acid tert-butyl ester

113247-53-3

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Basic information

Product Name: (S)-1-[(S)-2-((S)-3-tert-Butoxycarbonylamino-2-hydroxy-2-methyl-4-phenyl-butylamino)-propionyl]-pyrrolidine-2-carboxylic acid tert-butyl ester
Synonyms:
CAS NO:113247-53-3
Molecular Formula:
Molecular Weight: 519.682
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)-1-[(S)-2-((S)-3-tert-Butoxycarbonylamino-2-hydroxy-2-methyl-4-phenyl-butylamino)-propionyl]-pyrrolidine-2-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-[(S)-2-((S)-3-tert-Butoxycarbonylamino-2-hydroxy-2-methyl-4-phenyl-butylamino)-propionyl]-pyrrolidine-2-carboxylic acid tert-butyl ester(113247-53-3)
EPA Substance Registry System: (S)-1-[(S)-2-((S)-3-tert-Butoxycarbonylamino-2-hydroxy-2-methyl-4-phenyl-butylamino)-propionyl]-pyrrolidine-2-carboxylic acid tert-butyl ester(113247-53-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 113247-53-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 113247-53-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,2,4 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113247-53:
(8*1)+(7*1)+(6*3)+(5*2)+(4*4)+(3*7)+(2*5)+(1*3)=93
93 % 10 = 3
So 113247-53-3 is a valid CAS Registry Number.

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113247-53-3Relevant academic research and scientific papers

SYNTHESIS OF PEPTIDE DERIVED AMINO ALCOHOLS II. SYNTHETIC METHODOLOGY FOR THE PREPARATION OF TERTIARY ALCOHOLS

Godfrey, Lollie D.,Gordon, Eric M.,Langen, Derek J. Von

, p. 1603 - 1606 (2007/10/02)

Synthetic methods are described for the preparation of a series of tripeptide derived aminoalcohols (i.e., 2).These novel peptidyl tetiary alcohols are potential inhibitors of angiotensin converting enzyme (ACE).The synthetic targets resemble acyltripepti

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