Cas 335336-95-3,(1-benzylaminooxalyl-3,3,3-trifluoro-propyl)-carbamic acid <i>tert</i>-butyl ester

335336-95-3

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Basic information

Product Name: (1-benzylaminooxalyl-3,3,3-trifluoro-propyl)-carbamic acid tert-butyl ester
Synonyms: (1-benzylaminooxalyl-3,3,3-trifluoro-propyl)-carbamic acid tert-butyl ester
CAS NO:335336-95-3
Molecular Formula:
Molecular Weight: 374.36
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: (1-benzylaminooxalyl-3,3,3-trifluoro-propyl)-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1-benzylaminooxalyl-3,3,3-trifluoro-propyl)-carbamic acid tert-butyl ester(335336-95-3)
EPA Substance Registry System: (1-benzylaminooxalyl-3,3,3-trifluoro-propyl)-carbamic acid tert-butyl ester(335336-95-3)

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: 335336-95-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 335336-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,3,3 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 335336-95:
(8*3)+(7*3)+(6*5)+(5*3)+(4*3)+(3*6)+(2*9)+(1*5)=143
143 % 10 = 3
So 335336-95-3 is a valid CAS Registry Number.

335336-95-3Upstream product

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335336-95-3Relevant academic research and scientific papers

The identification of α-ketoamides as potent inhibitors of hepatitis C virus NS3-4A proteinase

Bennett,Campbell,Campbell,Carr,Dunsdon,Greening,Hurst,Jennings,Jones,Jordan,Kay,O'Brien,King-Underwood,Raynham,Wilkinson,Wilkinson,Wilson

, p. 355 - 357 (2001)

Peptides based upon the non-prime side residues of the NS4A-4B cleavage site of hepatitis C virus (HCV) NS3-4A proteinase containing an α-ketoamide moiety in place of the scissile amide bond are potent inhibitors of this enzyme.

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