Cas 1133161-70-2,benzyl 2,6-dideoxy-4-O-benzoyl-2-p-tolylthio-β-D-glucopyranosyl-(1->4)-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranoside

1133161-70-2

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Basic information

Product Name: benzyl 2,6-dideoxy-4-O-benzoyl-2-p-tolylthio-β-D-glucopyranosyl-(1->4)-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranoside
Synonyms:
CAS NO:1133161-70-2
Molecular Formula:
Molecular Weight: 734.649
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: benzyl 2,6-dideoxy-4-O-benzoyl-2-p-tolylthio-β-D-glucopyranosyl-(1->4)-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 2,6-dideoxy-4-O-benzoyl-2-p-tolylthio-β-D-glucopyranosyl-(1->4)-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranoside(1133161-70-2)
EPA Substance Registry System: benzyl 2,6-dideoxy-4-O-benzoyl-2-p-tolylthio-β-D-glucopyranosyl-(1->4)-2,6-dideoxy-2-iodo-3-C-methyl-α-L-mannopyranoside(1133161-70-2)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1133161-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1133161-70-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,3,1,6 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1133161-70:
(9*1)+(8*1)+(7*3)+(6*3)+(5*1)+(4*6)+(3*1)+(2*7)+(1*0)=102
102 % 10 = 2
So 1133161-70-2 is a valid CAS Registry Number.

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1133161-70-2Relevant academic research and scientific papers

2,3-Anhydrosugars in glycoside bond synthesis. Application to 2,6-dideoxypyranosides

Hou, Dianjie,Lowary, Todd L.

supporting information; experimental part, p. 2278 - 2289 (2009/08/07)

We describe here the first use of 2,3-anhydrosugars as glycosylating agents for the preparation of 2-deoxypyranosides. In particular, the methodology was used to assemble 2,6-dideoxysugar glycosides. Glycosylation of a panel of alcohols with one of two 6-

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