Cas 104017-01-8,(2S,4R,5R,6R)-2-Benzenesulfonyl-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-pyran-2-carboxylic acid methyl ester

104017-01-8

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Basic information

Product Name: (2S,4R,5R,6R)-2-Benzenesulfonyl-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-pyran-2-carboxylic acid methyl ester
Synonyms:
CAS NO:104017-01-8
Molecular Formula:
Molecular Weight: 689.146
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: (2S,4R,5R,6R)-2-Benzenesulfonyl-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-pyran-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,4R,5R,6R)-2-Benzenesulfonyl-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-pyran-2-carboxylic acid methyl ester(104017-01-8)
EPA Substance Registry System: (2S,4R,5R,6R)-2-Benzenesulfonyl-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-6-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-pyran-2-carboxylic acid methyl ester(104017-01-8)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 104017-01-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104017-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,1 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104017-01:
(8*1)+(7*0)+(6*4)+(5*0)+(4*1)+(3*7)+(2*0)+(1*1)=58
58 % 10 = 8
So 104017-01-8 is a valid CAS Registry Number.

104017-01-8Upstream product

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104017-01-8Relevant academic research and scientific papers

D-GLYCOPYRANOSYL PHENYLSULPHONES: ACYLATION OF THEIR LITHIATED ANIONS AND REDUCTIVE DESULFONYLATION OF THE RESULTING ACYLATED SULFONES. A SYNTHESIS OF α-D-GLYCOSIDES

Beau, Jean-Marie,Sinay, Pierre

, p. 6193 - 6196 (1985)

The lithiated anion of 3,4,6-tri-O-t-butyldimethylsilyl-2-deoxy-α,β-D-glucopyranosyl phenylsulfone reacts with dimethylcarbonate and various phenyl esters to give stable acylated products.Subsequent reductive lithiation leads to enolates which ungergo kin

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