Cas 666258-34-0,4-methoxyphenyl 3-O-allyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2,4,6-tri-O-acetyl-β-D-glucopyranoside

666258-34-0

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Basic information

Product Name: 4-methoxyphenyl 3-O-allyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2,4,6-tri-O-acetyl-β-D-glucopyranoside
Synonyms: 4-methoxyphenyl 3-O-allyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2,4,6-tri-O-acetyl-β-D-glucopyranoside
CAS NO:666258-34-0
Molecular Formula:
Molecular Weight: 806.818
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: 4-methoxyphenyl 3-O-allyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2,4,6-tri-O-acetyl-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 4-methoxyphenyl 3-O-allyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2,4,6-tri-O-acetyl-β-D-glucopyranoside(666258-34-0)
EPA Substance Registry System: 4-methoxyphenyl 3-O-allyl-2-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1->3)-2,4,6-tri-O-acetyl-β-D-glucopyranoside(666258-34-0)

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: 666258-34-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 666258-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,6,2,5 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 666258-34:
(8*6)+(7*6)+(6*6)+(5*2)+(4*5)+(3*8)+(2*3)+(1*4)=190
190 % 10 = 0
So 666258-34-0 is a valid CAS Registry Number.

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666258-34-0Relevant academic research and scientific papers

Synthesis of 3,6-Branched β-D-Glucose Oligosaccharides

Zeng, Youlin,Kong, Fanzuo

, p. 881 - 890 (2003)

A glucohexasaccharide, β-D-Glcp-(1→3)-[β-D-Glcp-(1→3)- β-D-Glcp-(1→6)]-β-D-Glcp-(1→3)-β-D-Glcp-(1→3) -β-D-Glcp was synthesized as its 4-methoxyphenyl glycosidevia 2 + 2 + 2 strategy with benzylidenated glucose mono- and disaccharides as the key intermedia

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