Cas 120199-98-6,(S)-1-[(S)-6-tert-Butoxycarbonylamino-2-((R)-1-ethoxycarbonyl-3-phenyl-propylamino)-hexanoyl]-pyrrolidine-2-carboxylic acid tert-butyl ester

120199-98-6

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Basic information

Product Name: (S)-1-[(S)-6-tert-Butoxycarbonylamino-2-((R)-1-ethoxycarbonyl-3-phenyl-propylamino)-hexanoyl]-pyrrolidine-2-carboxylic acid tert-butyl ester
Synonyms:
CAS NO:120199-98-6
Molecular Formula:
Molecular Weight: 589.773
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)-6-tert-Butoxycarbonylamino-2-((R)-1-ethoxycarbonyl-3-phenyl-propylamino)-hexanoyl]-pyrrolidine-2-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-[(S)-6-tert-Butoxycarbonylamino-2-((R)-1-ethoxycarbonyl-3-phenyl-propylamino)-hexanoyl]-pyrrolidine-2-carboxylic acid tert-butyl ester(120199-98-6)
EPA Substance Registry System: (S)-1-[(S)-6-tert-Butoxycarbonylamino-2-((R)-1-ethoxycarbonyl-3-phenyl-propylamino)-hexanoyl]-pyrrolidine-2-carboxylic acid tert-butyl ester(120199-98-6)

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: 120199-98-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 120199-98-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,1,9 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 120199-98:
(8*1)+(7*2)+(6*0)+(5*1)+(4*9)+(3*9)+(2*9)+(1*8)=116
116 % 10 = 6
So 120199-98-6 is a valid CAS Registry Number.

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120199-98-6Downstream Products

120199-98-6Relevant academic research and scientific papers

A Stereoselective Synthesis of N--L-alanine Derivatives by Means of Reductive Amination

Iwasaki, Genji,Kimura, Rieko,Numao, Naganori,Kondo, Kiyoshi

, p. 1691 - 1694 (1988)

A stereoselective synthesis of N--L-alanine, a portion of the molecule of angiotensin converting-enzyme(ACE) inhibitors, by reductive amination utilizing catecholborane and further applications of the reaction to the synthesis of ACE inhibitors are described.

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