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

167260-15-3

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Basic information

Product Name: (3S,4R)-3-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-4-(4-methoxy-benzyloxymethyl)-cyclopentanone
Synonyms: (3S,4R)-3-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-4-(4-methoxy-benzyloxymethyl)-cyclopentanone
CAS NO:167260-15-3
Molecular Formula:
Molecular Weight: 392.611
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: (3S,4R)-3-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-4-(4-methoxy-benzyloxymethyl)-cyclopentanone(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4R)-3-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-4-(4-methoxy-benzyloxymethyl)-cyclopentanone(167260-15-3)
EPA Substance Registry System: (3S,4R)-3-[Dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-4-(4-methoxy-benzyloxymethyl)-cyclopentanone(167260-15-3)

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: 167260-15-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 167260-15-3 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, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 167260-15:
(8*1)+(7*6)+(6*7)+(5*2)+(4*6)+(3*0)+(2*1)+(1*5)=133
133 % 10 = 3
So 167260-15-3 is a valid CAS Registry Number.

167260-15-3Upstream product

167260-15-3Downstream Products

167260-15-3Relevant academic research and scientific papers

An efficient synthesis of a chiral carbocyclic 2'-deoxyribonucleoside synthon by directed reduction

Borthwick,Crame,Exall,Weingarten

, p. 7677 - 7680 (1994)

Directed reduction of the 1,4 hydroxy-ketone 9 and the 1,4 aldehydo-ketone 12 with NaBH(OAc)3 gave stereoselectively in high yield the 1,4 diol 10, a key intermediate required in our synthesis of chiral carbocyclic 2'-deoxyribonucleosides

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