Cas 1260110-29-9,[6-(2,3-di-O-benzyl-1-ethylthio-β-D-glucopyranos-6-yl)-6-oxohexyl]-1-methyl-1H-imidazol-3-ium bromide

1260110-29-9

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Basic information

Product Name: [6-(2,3-di-O-benzyl-1-ethylthio-β-D-glucopyranos-6-yl)-6-oxohexyl]-1-methyl-1H-imidazol-3-ium bromide
Synonyms: [6-(2,3-di-O-benzyl-1-ethylthio-β-D-glucopyranos-6-yl)-6-oxohexyl]-1-methyl-1H-imidazol-3-ium bromide
CAS NO:1260110-29-9
Molecular Formula:
Molecular Weight: 663.673
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: [6-(2,3-di-O-benzyl-1-ethylthio-β-D-glucopyranos-6-yl)-6-oxohexyl]-1-methyl-1H-imidazol-3-ium bromide(CAS DataBase Reference)
NIST Chemistry Reference: [6-(2,3-di-O-benzyl-1-ethylthio-β-D-glucopyranos-6-yl)-6-oxohexyl]-1-methyl-1H-imidazol-3-ium bromide(1260110-29-9)
EPA Substance Registry System: [6-(2,3-di-O-benzyl-1-ethylthio-β-D-glucopyranos-6-yl)-6-oxohexyl]-1-methyl-1H-imidazol-3-ium bromide(1260110-29-9)

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: 1260110-29-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1260110-29-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,1,1 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1260110-29:
(9*1)+(8*2)+(7*6)+(6*0)+(5*1)+(4*1)+(3*0)+(2*2)+(1*9)=89
89 % 10 = 9
So 1260110-29-9 is a valid CAS Registry Number.

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1260110-29-9Relevant academic research and scientific papers

First examples of α-(1a→4)-Glycosylation reactions on ionic liquid supports

Pepin, Matthieu,Hubert-Roux, Marie,Martin, Claudette,Guillen, Frederic,Lange, Catherine,Gouhier, Geraldine

, p. 6366 - 6371 (2010)

We have developed the first α-(1a→4)-glycosylation reactions on ionic liquid supports. The purification steps involve simple liquid/liquid extractions. The positive influence of the soluble support on the stereoselectivity was proved, and the recyclable c

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