Cas 208102-18-5,2-[(2S,3R,4S,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-sulfonyl]-pyridine

208102-18-5

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Basic information

Product Name: 2-[(2S,3R,4S,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-sulfonyl]-pyridine
Synonyms: 2-[(2S,3R,4S,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-sulfonyl]-pyridine
CAS NO:208102-18-5
Molecular Formula:
Molecular Weight: 689.945
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: 2-[(2S,3R,4S,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-sulfonyl]-pyridine(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(2S,3R,4S,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-sulfonyl]-pyridine(208102-18-5)
EPA Substance Registry System: 2-[(2S,3R,4S,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-sulfonyl]-pyridine(208102-18-5)

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: 208102-18-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 208102-18-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,1,0 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 208102-18:
(8*2)+(7*0)+(6*8)+(5*1)+(4*0)+(3*2)+(2*1)+(1*8)=85
85 % 10 = 5
So 208102-18-5 is a valid CAS Registry Number.

208102-18-5Upstream product

18162-48-6 tert-butyldimethylsilyl chloride

208102-18-5Downstream Products

80040-79-5 3,4,6-tri-O-benzyl-D-galactal

208102-18-5Relevant academic research and scientific papers

A general approach to 1,2-trans-C-glycosides via glycosyl samarium(III) compounds

Skrydstrup, Troels,Jarreton, Olivier,Mazéas, Daniel,Urban, Dominique,Beau, Jean-Marie

, p. 655 - 671 (2007/10/03)

The samarium diiodide reduction of glycosyl pyridyl sulfones with ketones or aldehydes under Barbier conditions leads to the instantaneous and stereospecific formation of 1,2trans-C-glycosides in good to acceptable yields. Mannosyl pyridyl sulfones 5ac,h

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