Cas 901284-58-0,3-Oxazolidinecarboxylic acid, 4-[[[[[(1S)-2-methoxy-2-oxo-1-(phenylmethyl)ethyl]amino]carbonyl]amino ]methyl]-5-oxo-, 1,1-dimethylethyl ester, (4S)-

901284-58-0

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Basic information

Product Name: 3-Oxazolidinecarboxylic acid, 4-[[[[[(1S)-2-methoxy-2-oxo-1-(phenylmethyl)ethyl]amino]carbonyl]amino ]methyl]-5-oxo-, 1,1-dimethylethyl ester, (4S)-
Synonyms:
CAS NO:901284-58-0
Molecular Formula: C20H27N3O7
Molecular Weight: 421.45
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: 3-Oxazolidinecarboxylic acid, 4-[[[[[(1S)-2-methoxy-2-oxo-1-(phenylmethyl)ethyl]amino]carbonyl]amino ]methyl]-5-oxo-, 1,1-dimethylethyl ester, (4S)-(CAS DataBase Reference)
NIST Chemistry Reference: 3-Oxazolidinecarboxylic acid, 4-[[[[[(1S)-2-methoxy-2-oxo-1-(phenylmethyl)ethyl]amino]carbonyl]amino ]methyl]-5-oxo-, 1,1-dimethylethyl ester, (4S)-(901284-58-0)
EPA Substance Registry System: 3-Oxazolidinecarboxylic acid, 4-[[[[[(1S)-2-methoxy-2-oxo-1-(phenylmethyl)ethyl]amino]carbonyl]amino ]methyl]-5-oxo-, 1,1-dimethylethyl ester, (4S)-(901284-58-0)

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 901284-58-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 901284-58-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,1,2,8 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 901284-58:
(8*9)+(7*0)+(6*1)+(5*2)+(4*8)+(3*4)+(2*5)+(1*8)=150
150 % 10 = 0
So 901284-58-0 is a valid CAS Registry Number.

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901284-58-0Relevant academic research and scientific papers

A general and facile synthetic approach to Nα-Boc ureidoalanine derivatives

Teng, Hanbing,He, Yunjiao,Wu, Lamei,Su, Jiangtao,Feng, Xichun,Qiu, Guofu,Liang, Shucai,Hu, Xianming

, p. 877 - 880 (2006)

We report a new and facile synthetic approach to Nα-Boc ureidoalanine derivatives from commercially available Boc-L-aspartic acid. Not only N′-substituted but also N′,N′-disubstituted ureidoalanine derivatives may be obtained by this method. Th

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