Cas 474959-32-5,3,4-di-O-benzoyl-1,2-O-[(R)-ethylidene]-6-O-trityl-β-D-mannopyranose

474959-32-5

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Basic information

Product Name: 3,4-di-O-benzoyl-1,2-O-[(R)-ethylidene]-6-O-trityl-β-D-mannopyranose
Synonyms: 3,4-di-O-benzoyl-1,2-O-[(R)-ethylidene]-6-O-trityl-β-D-mannopyranose
CAS NO:474959-32-5
Molecular Formula:
Molecular Weight: 656.732
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: 3,4-di-O-benzoyl-1,2-O-[(R)-ethylidene]-6-O-trityl-β-D-mannopyranose(CAS DataBase Reference)
NIST Chemistry Reference: 3,4-di-O-benzoyl-1,2-O-[(R)-ethylidene]-6-O-trityl-β-D-mannopyranose(474959-32-5)
EPA Substance Registry System: 3,4-di-O-benzoyl-1,2-O-[(R)-ethylidene]-6-O-trityl-β-D-mannopyranose(474959-32-5)

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: 474959-32-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 474959-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,9,5 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 474959-32:
(8*4)+(7*7)+(6*4)+(5*9)+(4*5)+(3*9)+(2*3)+(1*2)=205
205 % 10 = 5
So 474959-32-5 is a valid CAS Registry Number.

474959-32-5Upstream product

474959-32-5Downstream Products

414878-05-0 1,2,6-tri-O-acetyl-3,4-di-O-benzoyl-α-D-mannopyranose

474959-32-5Relevant academic research and scientific papers

A highly efficient synthesis of an octasaccharide, the repeating unit of the cell-wall mannan of Trichophyton mentagrophytes and T. rubrum

Ning, Jun,Heng, Linsen,Kong, Fanzuo

, p. 1159 - 1164 (2007/10/03)

A highly concise and effective synthesis of the mannose octasaccharide repeating unit of the cell-wall mannan of Trichophyton mentagrophytes and T. rubrum was achieved via 6-O-glycosylation of a tetrasaccharide acceptor with a tetrasaccharide donor, follo

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