Cas 120629-64-3,<(S)-(benzyloxycarbonyl)-L-valyl>-N-<1-<<5-<<(tert-butyldimethylsilyl)oxy>methyl>benzoxazol-2-yl>carbonyl>-2-methylpropyl>-L-prolinamide

120629-64-3

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Basic information

Product Name: <(S)-(benzyloxycarbonyl)-L-valyl>-N-<1-<<5-<<(tert-butyldimethylsilyl)oxy>methyl>benzoxazol-2-yl>carbonyl>-2-methylpropyl>-L-prolinamide
Synonyms: <(S)-(benzyloxycarbonyl)-L-valyl>-N-<1-<<5-<<(tert-butyldimethylsilyl)oxy>methyl>benzoxazol-2-yl>carbonyl>-2-methylpropyl>-L-prolinamide
CAS NO:120629-64-3
Molecular Formula:
Molecular Weight: 692.928
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)-(benzyloxycarbonyl)-L-valyl>-N-<1-<<5-<<(tert-butyldimethylsilyl)oxy>methyl>benzoxazol-2-yl>carbonyl>-2-methylpropyl>-L-prolinamide(CAS DataBase Reference)
NIST Chemistry Reference: <(S)-(benzyloxycarbonyl)-L-valyl>-N-<1-<<5-<<(tert-butyldimethylsilyl)oxy>methyl>benzoxazol-2-yl>carbonyl>-2-methylpropyl>-L-prolinamide(120629-64-3)
EPA Substance Registry System: <(S)-(benzyloxycarbonyl)-L-valyl>-N-<1-<<5-<<(tert-butyldimethylsilyl)oxy>methyl>benzoxazol-2-yl>carbonyl>-2-methylpropyl>-L-prolinamide(120629-64-3)

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: 120629-64-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 120629-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,6,2 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 120629-64:
(8*1)+(7*2)+(6*0)+(5*6)+(4*2)+(3*9)+(2*6)+(1*4)=103
103 % 10 = 3
So 120629-64-3 is a valid CAS Registry Number.

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120629-64-3Relevant academic research and scientific papers

Peptidyl α-Ketoheterocyclic Inhibitors of Human Neutrophil Elastase. 3. In Vitro and in Vivo Potency of a Series of Peptidyl α-Ketobenzoxazoles

Edwards, Philip D.,Zottola, Mark A.,Davis, Matthew,Williams, Joseph,Tuthill, Paul A.

, p. 3972 - 3982 (2007/10/03)

A series of peptidyl α-ketobenzoxazoles were synthesized and evaluated for their in vitro and in vivo inhibition of human neutrophil elastase (HNE).These compounds inhibit HNE by forming both a covalent bond between the ketone carbonyl carbon atom and the

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