Cas 763129-73-3,phenyl 2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-1-thio-6-O-trifluoroethylsulfonate-α-D-glucopyranoside

763129-73-3

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Basic information

Product Name: phenyl 2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-1-thio-6-O-trifluoroethylsulfonate-α-D-glucopyranoside
Synonyms: phenyl 2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-1-thio-6-O-trifluoroethylsulfonate-α-D-glucopyranoside
CAS NO:763129-73-3
Molecular Formula:
Molecular Weight: 669.7
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: phenyl 2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-1-thio-6-O-trifluoroethylsulfonate-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: phenyl 2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-1-thio-6-O-trifluoroethylsulfonate-α-D-glucopyranoside(763129-73-3)
EPA Substance Registry System: phenyl 2-azido-3-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-1-thio-6-O-trifluoroethylsulfonate-α-D-glucopyranoside(763129-73-3)

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: 763129-73-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 763129-73-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,3,1,2 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 763129-73:
(8*7)+(7*6)+(6*3)+(5*1)+(4*2)+(3*9)+(2*7)+(1*3)=173
173 % 10 = 3
So 763129-73-3 is a valid CAS Registry Number.

763129-73-3Upstream product

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763129-73-3Relevant academic research and scientific papers

Trifluoroethylsulfonate protected monosaccharides in glycosylation reactions

Karst, Nathalie A.,Islam, Tasneem F.,Avci, Fikri Y.,Linhardt, Robert J.

, p. 6433 - 6437 (2007/10/03)

A variety of sulfo-protected monosaccharide donors and acceptors were investigated in glycosylation reactions. Trifluoroethylsulfonate (SO 3TFE) group was compatible with a wide range of activation conditions commonly used with fluoride, imidat

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