Cas 437757-84-1,benzyl 2,3,6-tri-O-benzyl-4-O-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside

437757-84-1

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Basic information

Product Name: benzyl 2,3,6-tri-O-benzyl-4-O-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside
Synonyms: benzyl 2,3,6-tri-O-benzyl-4-O-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside
CAS NO:437757-84-1
Molecular Formula:
Molecular Weight: 1079.36
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: benzyl 2,3,6-tri-O-benzyl-4-O-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 2,3,6-tri-O-benzyl-4-O-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside(437757-84-1)
EPA Substance Registry System: benzyl 2,3,6-tri-O-benzyl-4-O-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside(437757-84-1)

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: 437757-84-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 437757-84-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,7,7,5 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 437757-84:
(8*4)+(7*3)+(6*7)+(5*7)+(4*5)+(3*7)+(2*8)+(1*4)=191
191 % 10 = 1
So 437757-84-1 is a valid CAS Registry Number.

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437757-84-1Relevant academic research and scientific papers

A new route to exo-glycals using the Ramberg-Baecklund rearrangement

Griffin, Frank K.,Paterson, Duncan E.,Murphy, Paul V.,Taylor, Richard J. K.

, p. 1305 - 1322 (2007/10/03)

A new route to exo-glycals 4 is described in which glycosyl sulfones 3 are subjected to the Meyers variant of the Ramberg-Baecklund rearrangement. The conversion of sulfones derived from glucose, galactose, mannose, cellobiose, and ribose into di-, tri-, and tetra-substituted alkenes is reported. Preliminary mechanistic studies of this process are also described. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

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