Cas 323582-16-7,Methanesulfonic acid (1S,2S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-4,4-bis-ethylsulfanyl-butyl ester

323582-16-7

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Basic information

Product Name: Methanesulfonic acid (1S,2S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-4,4-bis-ethylsulfanyl-butyl ester
Synonyms:
CAS NO:323582-16-7
Molecular Formula:
Molecular Weight: 647.009
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: Methanesulfonic acid (1S,2S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-4,4-bis-ethylsulfanyl-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Methanesulfonic acid (1S,2S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-4,4-bis-ethylsulfanyl-butyl ester(323582-16-7)
EPA Substance Registry System: Methanesulfonic acid (1S,2S)-2-benzyloxy-1-(tert-butyl-diphenyl-silanyloxymethyl)-4,4-bis-ethylsulfanyl-butyl ester(323582-16-7)

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: 323582-16-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 323582-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,3,5,8 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 323582-16:
(8*3)+(7*2)+(6*3)+(5*5)+(4*8)+(3*2)+(2*1)+(1*6)=127
127 % 10 = 7
So 323582-16-7 is a valid CAS Registry Number.

323582-16-7Upstream product

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323582-16-7Relevant academic research and scientific papers

A novel synthesis of 4'-thionucleosides and a potential stereospecific route to pyrimidine nucleosides

Miller,Pugh,Ullah,Gutteridge

, p. 10099 - 10105 (2007/10/03)

Starting with the L-ascorbate derived epoxide 1, a di-t-butyl dithioacetal cyclisation route to 2'-deoxy-4'-thionucleosides has been developed. Based on an intermediate in this route, a novel and stereospecific route to α- or β-pyrimidine nucleosides has been conceived, but its implementation failed at a key ring-closure step. (C) 2000 Elsevier Science Ltd.

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