Cas 1032633-93-4,methyl 2,3,4-tri-O-benzoyl-6-S-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-6-thio-α-D-glucopyranose

1032633-93-4

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Basic information

Product Name: methyl 2,3,4-tri-O-benzoyl-6-S-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-6-thio-α-D-glucopyranose
Synonyms: methyl 2,3,4-tri-O-benzoyl-6-S-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-6-thio-α-D-glucopyranose
CAS NO:1032633-93-4
Molecular Formula:
Molecular Weight: 967.016
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 2,3,4-tri-O-benzoyl-6-S-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-6-thio-α-D-glucopyranose(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2,3,4-tri-O-benzoyl-6-S-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-6-thio-α-D-glucopyranose(1032633-93-4)
EPA Substance Registry System: methyl 2,3,4-tri-O-benzoyl-6-S-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-6-thio-α-D-glucopyranose(1032633-93-4)

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: 1032633-93-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1032633-93-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,6,3 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1032633-93:
(9*1)+(8*0)+(7*3)+(6*2)+(5*6)+(4*3)+(3*3)+(2*9)+(1*3)=114
114 % 10 = 4
So 1032633-93-4 is a valid CAS Registry Number.

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1032633-93-4Relevant academic research and scientific papers

Two straightforward strategies for the synthesis of thiodisaccharides with a furanose unit as the nonreducing end

Repetto, Evangelina,Marino, Carla,Uhrig, M. Laura,Varela, Oscar

, p. 540 - 547 (2008/09/18)

Thiodisaccharides having a 1-thiopentofuranose nonreducing end were synthesized by two routes starting from per-O-acylaldofuranoses with arabino, ribo, and xylo configurations. These glycosyl donors were converted into S-glycosyl isothiourea derivatives a

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