Cas 167260-22-2,(1S,3S,4R)-3-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-4-(4-methoxy-benzyloxymethyl)-cyclopentanol

167260-22-2

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Basic information

Product Name: (1S,3S,4R)-3-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-4-(4-methoxy-benzyloxymethyl)-cyclopentanol
Synonyms:
CAS NO:167260-22-2
Molecular Formula:
Molecular Weight: 394.627
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: (1S,3S,4R)-3-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-4-(4-methoxy-benzyloxymethyl)-cyclopentanol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,3S,4R)-3-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-4-(4-methoxy-benzyloxymethyl)-cyclopentanol(167260-22-2)
EPA Substance Registry System: (1S,3S,4R)-3-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-4-(4-methoxy-benzyloxymethyl)-cyclopentanol(167260-22-2)

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: 167260-22-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 167260-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,2,6 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 167260-22:
(8*1)+(7*6)+(6*7)+(5*2)+(4*6)+(3*0)+(2*2)+(1*2)=132
132 % 10 = 2
So 167260-22-2 is a valid CAS Registry Number.

167260-22-2Upstream product

167260-15-3 (3S,4R)-3-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-4-(4-methoxy-benzyloxymethyl)-cyclopentanone

167260-22-2Downstream Products

167260-22-2Relevant academic research and scientific papers

A short, convergent synthesis of two chiral antiviral agents, (+) carbocyclic 2′-deoxy-5-[(E)-2-bromovinyl] uridine and (+) carbocyclic 2′-deoxyguanosine

Borthwick, Alan D.,Crame, Andrew J.,Exall, Anne M.,Weingarten, Gordon G.,Mahmoudian, Mahmuod

, p. 6929 - 6932 (1995)

Stereo selective microbial reduction of ketone 2 gave the alcohol 5 which was coupled under Mitsunobu conditions with the protected pyrimidine 7 and purine 10 to give on deprotection the chiral antiviral nucleosides (+) carbocyclic 2′-deoxy-5-[(E)-2bromov

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