Cas 220835-89-2,methyl 2-O-diphenylmethoxymethyl-4,6-O-diphenylmethylene-α-D-glucopyranoside

220835-89-2

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Basic information

Product Name: methyl 2-O-diphenylmethoxymethyl-4,6-O-diphenylmethylene-α-D-glucopyranoside
Synonyms: methyl 2-O-diphenylmethoxymethyl-4,6-O-diphenylmethylene-α-D-glucopyranoside
CAS NO:220835-89-2
Molecular Formula:
Molecular Weight: 554.64
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-O-diphenylmethoxymethyl-4,6-O-diphenylmethylene-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-O-diphenylmethoxymethyl-4,6-O-diphenylmethylene-α-D-glucopyranoside(220835-89-2)
EPA Substance Registry System: methyl 2-O-diphenylmethoxymethyl-4,6-O-diphenylmethylene-α-D-glucopyranoside(220835-89-2)

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: 220835-89-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 220835-89-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,8,3 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 220835-89:
(8*2)+(7*2)+(6*0)+(5*8)+(4*3)+(3*5)+(2*8)+(1*9)=122
122 % 10 = 2
So 220835-89-2 is a valid CAS Registry Number.

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220835-89-2Relevant academic research and scientific papers

A simple procedure for the development of acld-labile protecting groups on position 2 and 3 of methyl α-D-glucopyranoside

Di Donna, Leonardo,Napoli, Anna,Siciliano, Carlo,Sindona, Giovanni

, p. 1013 - 1014 (1999)

Building blocks of methyl α-D-glucopyranoside possessing free hydroxyl functions in the position 2 or 3 and orthogonal acid-labile protecting groups on the other reacting sites can be conveniently prepared by means of benzophenone dimethyl ketal under ver

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