Cas 1272660-75-9,(2R,1'S)-2-benzyl-1-benzyloxycarbonyl-2-[(1'-benzylcarbamoyl)ethyl]carbamoylazetidine

1272660-75-9

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Basic information

Product Name: (2R,1'S)-2-benzyl-1-benzyloxycarbonyl-2-[(1'-benzylcarbamoyl)ethyl]carbamoylazetidine
Synonyms: (2R,1'S)-2-benzyl-1-benzyloxycarbonyl-2-[(1'-benzylcarbamoyl)ethyl]carbamoylazetidine
CAS NO:1272660-75-9
Molecular Formula:
Molecular Weight: 485.583
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: (2R,1'S)-2-benzyl-1-benzyloxycarbonyl-2-[(1'-benzylcarbamoyl)ethyl]carbamoylazetidine(CAS DataBase Reference)
NIST Chemistry Reference: (2R,1'S)-2-benzyl-1-benzyloxycarbonyl-2-[(1'-benzylcarbamoyl)ethyl]carbamoylazetidine(1272660-75-9)
EPA Substance Registry System: (2R,1'S)-2-benzyl-1-benzyloxycarbonyl-2-[(1'-benzylcarbamoyl)ethyl]carbamoylazetidine(1272660-75-9)

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: 1272660-75-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1272660-75-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,2,6,6 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1272660-75:
(9*1)+(8*2)+(7*7)+(6*2)+(5*6)+(4*6)+(3*0)+(2*7)+(1*5)=159
159 % 10 = 9
So 1272660-75-9 is a valid CAS Registry Number.

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1272660-75-9Relevant academic research and scientific papers

Synthesis and SAR studies on azetidine-containing dipeptides as HCMV inhibitors

Pérez-Faginas, Paula,Aranda, M. Teresa,García-López, M. Teresa,Snoeck, Robert,Andrei, Graciela,Balzarini, Jan,González-Mu?iz, Rosario

, p. 1155 - 1161 (2011/03/22)

SAR studies on an azetidine-containing dipeptide prototype inhibitor of HCMV are described. Three series of structurally modified analogues, involving substitutions at the N- and C-terminus, and at the C-terminal side-chain were synthesized and evaluated

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