Cas 497947-62-3,Carbamic acid, [(1S)-1-[cyano(triphenylphosphoranylidene)acetyl]pentyl]-, 1,1-dimethylethyl ester

497947-62-3

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Basic information

Product Name: Carbamic acid, [(1S)-1-[cyano(triphenylphosphoranylidene)acetyl]pentyl]-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:497947-62-3
Molecular Formula: C31H35N2O3P
Molecular Weight: 514.604
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: Carbamic acid, [(1S)-1-[cyano(triphenylphosphoranylidene)acetyl]pentyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [(1S)-1-[cyano(triphenylphosphoranylidene)acetyl]pentyl]-, 1,1-dimethylethyl ester(497947-62-3)
EPA Substance Registry System: Carbamic acid, [(1S)-1-[cyano(triphenylphosphoranylidene)acetyl]pentyl]-, 1,1-dimethylethyl ester(497947-62-3)

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: 497947-62-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 497947-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,9,4 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 497947-62:
(8*4)+(7*9)+(6*7)+(5*9)+(4*4)+(3*7)+(2*6)+(1*2)=233
233 % 10 = 3
So 497947-62-3 is a valid CAS Registry Number.

497947-62-3Upstream product

497947-62-3Downstream Products

497947-62-3Relevant academic research and scientific papers

Design of small molecule ketoamide-based inhibitors of cathepsin K

Catalano, John G.,Deaton, David N.,Long, Stacey T.,McFadyen, Robert B.,Miller, Larry R.,Payne, J. Alan,Wells-Knecht, Kevin J.,Wright, Lois L.

, p. 719 - 722 (2007/10/03)

A novel series of ketoamide-based inhibitors of cathepsin K has been identified. Modifications to P2 and P3 elements were crucial to enhancing inhibitory activity. Although not optimized, a selected inhibitor was effective in attenua

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