Cas 79218-69-2,methyl 6-O-(2-O-acetyl-3,4,6-O-benzyl-α-D-mannopyranosyl)-2,4-di-O-benzyl-α-D-mannopyranoside

79218-69-2

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Basic information

Product Name: methyl 6-O-(2-O-acetyl-3,4,6-O-benzyl-α-D-mannopyranosyl)-2,4-di-O-benzyl-α-D-mannopyranoside
Synonyms:
CAS NO:79218-69-2
Molecular Formula:
Molecular Weight: 848.987
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 6-O-(2-O-acetyl-3,4,6-O-benzyl-α-D-mannopyranosyl)-2,4-di-O-benzyl-α-D-mannopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 6-O-(2-O-acetyl-3,4,6-O-benzyl-α-D-mannopyranosyl)-2,4-di-O-benzyl-α-D-mannopyranoside(79218-69-2)
EPA Substance Registry System: methyl 6-O-(2-O-acetyl-3,4,6-O-benzyl-α-D-mannopyranosyl)-2,4-di-O-benzyl-α-D-mannopyranoside(79218-69-2)

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: 79218-69-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79218-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,1 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79218-69:
(7*7)+(6*9)+(5*2)+(4*1)+(3*8)+(2*6)+(1*9)=162
162 % 10 = 2
So 79218-69-2 is a valid CAS Registry Number.

79218-69-2Upstream product

68601-71-8 C₇₉H₈₆O₁₈

79218-69-2Downstream Products

79218-69-2Relevant academic research and scientific papers

Syntheses of model oligosaccharides of biological significance. Synthesis of methyl 3,6-di-O-(alpha-D-mannopyranosyl)-alpha-d-mannopyranoside and the corresponding mannobiosides.

Winnik,Brisson,Carver,Krepinsky

, p. 15 - 28 (1982)

Methyl 2-O-allyl-4,6-O-benzylidene-3-O-(2,3,4,6-tetra-O-acetyl-alpha-D-mannopyranosyl) -alpha-D-mannopyranoside (12) was prepared in 90% yield by Helferich glycosylation of methyl 2-O-allyl-4,6-O-benzylidene-alpha-D-mannopyranoside (9) with tetra-O-acetyl

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