Cas 112271-10-0,(4S)-4-<(tert-butyloxycarbonyl)amino>-5-<1-<(4-methylphenylsulphonyl)>imidazol-4-yl>-3-oxopentanoic acid ethyl ester

112271-10-0

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Basic information

Product Name: (4S)-4-<(tert-butyloxycarbonyl)amino>-5-<1-<(4-methylphenylsulphonyl)>imidazol-4-yl>-3-oxopentanoic acid ethyl ester
Synonyms:
CAS NO:112271-10-0
Molecular Formula:
Molecular Weight: 479.554
EINECS: N/A
Product Categories: N/A
Mol File: 112271-10-0.mol
Article Data: 1

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: (4S)-4-<(tert-butyloxycarbonyl)amino>-5-<1-<(4-methylphenylsulphonyl)>imidazol-4-yl>-3-oxopentanoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4S)-4-<(tert-butyloxycarbonyl)amino>-5-<1-<(4-methylphenylsulphonyl)>imidazol-4-yl>-3-oxopentanoic acid ethyl ester(112271-10-0)
EPA Substance Registry System: (4S)-4-<(tert-butyloxycarbonyl)amino>-5-<1-<(4-methylphenylsulphonyl)>imidazol-4-yl>-3-oxopentanoic acid ethyl ester(112271-10-0)

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: 112271-10-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112271-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,7 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112271-10:
(8*1)+(7*1)+(6*2)+(5*2)+(4*7)+(3*1)+(2*1)+(1*0)=70
70 % 10 = 0
So 112271-10-0 is a valid CAS Registry Number.

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112271-10-0Relevant articles and documents

A Facile Synthesis of Statine and Analogues by Reduction of β-Keto Esters Derived from Boc-Protected Amino Acids. HPLC Analyses of Their Enantiomeric Purity

Maibaum, Juergen,Rich, Daniel H.

, p. 869 - 873 (1988)

The synthesis of γ-amino-β-keto ester derivatives 3a-e from N-Boc-protected L-amino acids by N,N'-carbonyldiimidazole activation and treatment with the magnesium enolate of hydrogen ethyl malonate is described.Racemization during activation, which depende

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