Cas 664341-76-8,Imidazo[4,5-d][1,3]diazepine, 8-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[(1S,3R)-3-[[[(1,1-dimethylethyl )diphenylsilyl]oxy]methyl]cyclopentyl]-3,4,7,8-tetrahydro-, (8R)-

664341-76-8

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Basic information

Product Name: Imidazo[4,5-d][1,3]diazepine, 8-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[(1S,3R)-3-[[[(1,1-dimethylethyl )diphenylsilyl]oxy]methyl]cyclopentyl]-3,4,7,8-tetrahydro-, (8R)-
Synonyms:
CAS NO:664341-76-8
Molecular Formula: C34H50N4O2Si2
Molecular Weight: 602.968
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: Imidazo[4,5-d][1,3]diazepine, 8-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[(1S,3R)-3-[[[(1,1-dimethylethyl )diphenylsilyl]oxy]methyl]cyclopentyl]-3,4,7,8-tetrahydro-, (8R)-(CAS DataBase Reference)
NIST Chemistry Reference: Imidazo[4,5-d][1,3]diazepine, 8-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[(1S,3R)-3-[[[(1,1-dimethylethyl )diphenylsilyl]oxy]methyl]cyclopentyl]-3,4,7,8-tetrahydro-, (8R)-(664341-76-8)
EPA Substance Registry System: Imidazo[4,5-d][1,3]diazepine, 8-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-[(1S,3R)-3-[[[(1,1-dimethylethyl )diphenylsilyl]oxy]methyl]cyclopentyl]-3,4,7,8-tetrahydro-, (8R)-(664341-76-8)

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: 664341-76-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 664341-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,4,3,4 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 664341-76:
(8*6)+(7*6)+(6*4)+(5*3)+(4*4)+(3*1)+(2*7)+(1*6)=168
168 % 10 = 8
So 664341-76-8 is a valid CAS Registry Number.

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664341-76-8Relevant academic research and scientific papers

An efficient procedure for the preparation of (1S,3R)- and (1S,3S)-1-amino-3-(hydroxymethyl)cyclopentanes

Rapoport, Henry,Chen, Yuewu,Mohareb, Rafat M.,Ahn, Jin Hee,Sim, Tae Bo,Ho, Jonathan Z.

, p. 1153 - 1156 (2007/10/03)

Enantiomerically pure (1S,3S)- and (1S,3R)-1-amino-3-(hydroxymethyl) cyclopentanes have been efficiently synthesized from L-aspartic acid. The title compounds are isosteres of ribose and may be used to construct nucleoside analogs with important antiviral

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