Cas 1363732-67-5,methyl 3,4-di-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->2)-3-O-benzyl-4,6-O-benylidene-α-D-galactopyranoside

1363732-67-5

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Basic information

Product Name: methyl 3,4-di-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->2)-3-O-benzyl-4,6-O-benylidene-α-D-galactopyranoside
Synonyms: methyl 3,4-di-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->2)-3-O-benzyl-4,6-O-benylidene-α-D-galactopyranoside
CAS NO:1363732-67-5
Molecular Formula:
Molecular Weight: 816.902
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: methyl 3,4-di-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->2)-3-O-benzyl-4,6-O-benylidene-α-D-galactopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 3,4-di-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->2)-3-O-benzyl-4,6-O-benylidene-α-D-galactopyranoside(1363732-67-5)
EPA Substance Registry System: methyl 3,4-di-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(1->2)-3-O-benzyl-4,6-O-benylidene-α-D-galactopyranoside(1363732-67-5)

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: 1363732-67-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1363732-67-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,7,3 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1363732-67:
(9*1)+(8*3)+(7*6)+(6*3)+(5*7)+(4*3)+(3*2)+(2*6)+(1*7)=165
165 % 10 = 5
So 1363732-67-5 is a valid CAS Registry Number.

1363732-67-5Upstream product

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1363732-67-5Relevant academic research and scientific papers

Solvent-induced anomeric diastereoselectivity switching using a single glycosyl donor

Fujiwara, Ryuta,Horito, Shigeomi

, p. 2098 - 2103 (2011/11/06)

Highly diastereoselective glycosylation reactions have been developed; however, not all glycosylation reactions are diastereoselective and these reactions have probably not been reported. For some fucosylation reactions, unusually low or abnormally opposi

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