Cas 1309834-91-0,p-tolyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzyl-thio-β-D-glucopyranoside

1309834-91-0

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Basic information

Product Name: p-tolyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzyl-thio-β-D-glucopyranoside
Synonyms: p-tolyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzyl-thio-β-D-glucopyranoside
CAS NO:1309834-91-0
Molecular Formula:
Molecular Weight: 1079.36
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-tolyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzyl-thio-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: p-tolyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzyl-thio-β-D-glucopyranoside(1309834-91-0)
EPA Substance Registry System: p-tolyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzyl-thio-β-D-glucopyranoside(1309834-91-0)

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: 1309834-91-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1309834-91-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,8,3 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1309834-91:
(9*1)+(8*3)+(7*0)+(6*9)+(5*8)+(4*3)+(3*4)+(2*9)+(1*1)=170
170 % 10 = 0
So 1309834-91-0 is a valid CAS Registry Number.

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1309834-91-0Relevant academic research and scientific papers

Dimethylformamide: An unusual glycosylation modulator

Lu, Shao-Ru,Lai, Yen-Hsun,Chen, Jiun-Han,Liu, Chih-Yueh,Mong, Kwok-Kong Tony

supporting information; experimental part, p. 7315 - 7320 (2011/10/04)

A simple solution: When N,N-dimethylformamide was used to direct the stereochemical course of glycosylation reactions, 1,2-cis glycosylation products were formed with excellent selectivity. A straightforward highly α-stereoselective glycosylation involvin

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