Cas 136090-75-0,6'-O-acetyl-2',3'-di-O-benzyl-α-D-glucopyranosyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside

136090-75-0

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Basic information

Product Name: 6'-O-acetyl-2',3'-di-O-benzyl-α-D-glucopyranosyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside
Synonyms: 6'-O-acetyl-2',3'-di-O-benzyl-α-D-glucopyranosyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside
CAS NO:136090-75-0
Molecular Formula:
Molecular Weight: 832.945
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: 6'-O-acetyl-2',3'-di-O-benzyl-α-D-glucopyranosyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 6'-O-acetyl-2',3'-di-O-benzyl-α-D-glucopyranosyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside(136090-75-0)
EPA Substance Registry System: 6'-O-acetyl-2',3'-di-O-benzyl-α-D-glucopyranosyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside(136090-75-0)

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: 136090-75-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 136090-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,0,9 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 136090-75:
(8*1)+(7*3)+(6*6)+(5*0)+(4*9)+(3*0)+(2*7)+(1*5)=120
120 % 10 = 0
So 136090-75-0 is a valid CAS Registry Number.

136090-75-0Upstream product

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136090-75-0Relevant academic research and scientific papers

α-D-Glycosyl-Substituted α,α-D-Trehaloses with (1 -> 4)-Linkage: Syntheses and NMR Investigations

Wessel, Hans Peter,Englert, Gerhard,Stangier, Peter

, p. 682 - 696 (2007/10/02)

Two symmetrical trehalose glycosyl 'acceptors' 4 and 6 were prepared and three of the unsymmetrical type, 8, 10, and 11.Glucosylation of symmetrical 'acceptor'4 gave a higher yield of trisaccharide (44percent) than protective-group manipulation, namely vi

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