Cas 116173-83-2,[(S)-1-((S)-4-Benzyl-4,5-dihydro-oxazol-2-ylmethyl)-2-methyl-propyl]-carbamic acid methyl ester

116173-83-2

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Basic information

Product Name: [(S)-1-((S)-4-Benzyl-4,5-dihydro-oxazol-2-ylmethyl)-2-methyl-propyl]-carbamic acid methyl ester
Synonyms:
CAS NO:116173-83-2
Molecular Formula:
Molecular Weight: 304.389
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)-4-Benzyl-4,5-dihydro-oxazol-2-ylmethyl)-2-methyl-propyl]-carbamic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-1-((S)-4-Benzyl-4,5-dihydro-oxazol-2-ylmethyl)-2-methyl-propyl]-carbamic acid methyl ester(116173-83-2)
EPA Substance Registry System: [(S)-1-((S)-4-Benzyl-4,5-dihydro-oxazol-2-ylmethyl)-2-methyl-propyl]-carbamic acid methyl ester(116173-83-2)

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: 116173-83-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 116173-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,7 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 116173-83:
(8*1)+(7*1)+(6*6)+(5*1)+(4*7)+(3*3)+(2*8)+(1*3)=112
112 % 10 = 2
So 116173-83-2 is a valid CAS Registry Number.

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116173-83-2Relevant academic research and scientific papers

NEW SYNTHESIS OF β-AMINO ACIDS BY NUCLEOPHILIC ADDITION OF ENOLATE ANIONS TO N-METHOXYCARBONYLIMINES GENERATED FROM α-METHOXY CARBAMATES.

Shono, Tatsuya,Kise, Naoki,Sanda, Fumio,Ohi, Satoru,Tsubata, Kenji

, p. 231 - 234 (2007/10/02)

The nucleophilic addition of enolate anions of alkyl acetates to N-methoxycarbonylimines generated from α-methoxy carbamates gave β-amino acid derivates (3) and enantioselective synthesis (72-90percentee) of 3 was achieved by using chiral 2-methyloxazolines instead of acetates.

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