Cas 176165-22-3,p-methoxyphenyl 2,3-di-O-benzoyl-6-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside

176165-22-3

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Basic information

Product Name: p-methoxyphenyl 2,3-di-O-benzoyl-6-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside
Synonyms: p-methoxyphenyl 2,3-di-O-benzoyl-6-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside
CAS NO:176165-22-3
Molecular Formula:
Molecular Weight: 1107.26
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: p-methoxyphenyl 2,3-di-O-benzoyl-6-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: p-methoxyphenyl 2,3-di-O-benzoyl-6-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside(176165-22-3)
EPA Substance Registry System: p-methoxyphenyl 2,3-di-O-benzoyl-6-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside(176165-22-3)

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: 176165-22-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 176165-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,1,6 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 176165-22:
(8*1)+(7*7)+(6*6)+(5*1)+(4*6)+(3*5)+(2*2)+(1*2)=143
143 % 10 = 3
So 176165-22-3 is a valid CAS Registry Number.

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176165-22-3Relevant academic research and scientific papers

Synthesis of double-chain bis-sulfone neoglycolipids of the 2-, 3-, and 6-deoxyglobotrioses

Zhang, Zhiyuan,Magnusson, Goeran

, p. 2383 - 2393 (2007/10/03)

Partially protected 2-(trimethylsilyl)ethyl 2- and 3-deoxyglucosides and 6-deoxylactoside were synthesised via various routes and glycosylated with galabiosyl and galactosyl donors to give the corresponding deoxytrisaccharides. Removal of the protecting g

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