Cas 173910-83-3,methyl 3,4,6-tri-O-benzyl-β-D-mannopyranosyl-(1->6)-2,3-di-O-benzyl-α-D-glucopyranoside

173910-83-3

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Basic information

Product Name: methyl 3,4,6-tri-O-benzyl-β-D-mannopyranosyl-(1->6)-2,3-di-O-benzyl-α-D-glucopyranoside
Synonyms: methyl 3,4,6-tri-O-benzyl-β-D-mannopyranosyl-(1->6)-2,3-di-O-benzyl-α-D-glucopyranoside
CAS NO:173910-83-3
Molecular Formula:
Molecular Weight: 806.95
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 3,4,6-tri-O-benzyl-β-D-mannopyranosyl-(1->6)-2,3-di-O-benzyl-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 3,4,6-tri-O-benzyl-β-D-mannopyranosyl-(1->6)-2,3-di-O-benzyl-α-D-glucopyranoside(173910-83-3)
EPA Substance Registry System: methyl 3,4,6-tri-O-benzyl-β-D-mannopyranosyl-(1->6)-2,3-di-O-benzyl-α-D-glucopyranoside(173910-83-3)

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: 173910-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 173910-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,9,1 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 173910-83:
(8*1)+(7*7)+(6*3)+(5*9)+(4*1)+(3*0)+(2*8)+(1*3)=143
143 % 10 = 3
So 173910-83-3 is a valid CAS Registry Number.

173910-83-3Upstream product

358351-64-1 2-O-prop-1'-enyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl fluoride

173910-83-3Downstream Products

55094-26-3 methyl 2,3,4-tri-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-β-D-mannopyranosyl)-α-D-glucopyranoside

173910-83-3Relevant academic research and scientific papers

Allyl protecting group mediated intramolecular aglycon delivery: Optimisation of mixed acetal formation and mechanistic investigation

Cumpstey, Ian,Chayajarus, Kampanart,Fairbanks, Antony J.,Redgrave, Alison J.,Seward, Christopher M.P.

, p. 3207 - 3221 (2007/10/03)

An efficient protocol for the formation of α-iodo mixed acetals, the first step of allyl-mediated IAD, by reaction of allyl-derived enol ethers and alcohols, using I2, AgOTf and di-tert-butyl methylpyridine as a novel source of I+, i

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