Cas 85386-53-4,allyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->2)-O-(3,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside

85386-53-4

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Basic information

Product Name: allyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->2)-O-(3,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside
Synonyms:
CAS NO:85386-53-4
Molecular Formula:
Molecular Weight: 1200.43
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: allyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->2)-O-(3,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: allyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->2)-O-(3,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside(85386-53-4)
EPA Substance Registry System: allyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->2)-O-(3,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside(85386-53-4)

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: 85386-53-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85386-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,8 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85386-53:
(7*8)+(6*5)+(5*3)+(4*8)+(3*6)+(2*5)+(1*3)=164
164 % 10 = 4
So 85386-53-4 is a valid CAS Registry Number.

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85386-53-4Relevant academic research and scientific papers

Oligosaccharides from "standardized intermediates". Synthesis of a branched tetrasaccharide glycoside isomeric with the blood-group B, type 2 determinant.

Nashed,Anderson

, p. 43 - 52 (2007/10/02)

Building block derivatives of the component monosaccharides were used to construct the tetrasaccharide glycoside 15, in which an alpha-D-Galp-(1 leads to 4)-D-Gal linkage replaces the alpha-(1 leads to 3) linkage of the human blood-group B, type 2, determ

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