Cas 1225199-10-9,methyl 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-6-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-glucopyranoside

1225199-10-9

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Basic information

Product Name: methyl 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-6-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-glucopyranoside
Synonyms:
CAS NO:1225199-10-9
Molecular Formula:
Molecular Weight: 1227.37
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-di-O-benzyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-6-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-6-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-glucopyranoside(1225199-10-9)
EPA Substance Registry System: methyl 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-6-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-α-D-glucopyranoside(1225199-10-9)

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: 1225199-10-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1225199-10-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,5,1,9 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1225199-10:
(9*1)+(8*2)+(7*2)+(6*5)+(5*1)+(4*9)+(3*9)+(2*1)+(1*0)=139
139 % 10 = 9
So 1225199-10-9 is a valid CAS Registry Number.

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1225199-10-9Relevant academic research and scientific papers

[bmim][OTf] as co-solvent/promoter in room temperature reactivity-based one-pot glycosylation reactions

Galan, M. Carmen,Tran, Anh Tuan,Whitaker, Simon

supporting information; experimental part, p. 2106 - 2108 (2010/07/14)

[bmim][OTf] can promote regio- and chemo-selective glycosylation reactions at room temperature. Furthermore, the applicability to ambient three-component reactivity-based one-pot glycosylation reactions is demonstrated for the synthesis of several trisacc

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