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2-(trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-4-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128200-62-4

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128200-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128200-62-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,2,0 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 128200-62:
(8*1)+(7*2)+(6*8)+(5*2)+(4*0)+(3*0)+(2*6)+(1*2)=94
94 % 10 = 4
So 128200-62-4 is a valid CAS Registry Number.

128200-62-4Upstream product

128200-62-4Relevant academic research and scientific papers

METHOD FOR TREATING GALABIOSE-BINDING BACTERIA INFECTIONS

-

, (2008/06/13)

A method for treating infections caused by galabiose-binding bacteria using galabiose derivatives modified at the 3 and anomeric positions. The galabiose-derivatives and compositions of some are also disclosed

Synthesis of the globotetraose tetrasaccharide and terminal tri- and di-saccharide fragments

Nilsson, Ulf,Ray, Asim K.,Magnusson, Goeran

, p. 117 - 136 (2007/10/02)

The 2-(trimethylsilyl)ethyl (TMSEt) β-glycosides of globotetraose 3)-α-D-Gal-(1 -> 4)-β-D-Gal-(1 -> 4)-D-Glc> and the terminal trisaccharide, as well as the methyl α-glycoside 1 of the terminal disaccharide, were synthesised by silver trifluoromethanesulfonate-promoted β-glycosylation of suitably protected galactoside, galabioside, and globotrioside alcohols with 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl chloride, followed by removal of protecting groups.Removal of the anomeric TMSEt group of the globotetraoside and of the terminal trisaccharide, using trifluoroacetic acid-dichloromethane, gave the corresponding hemiacetal sugars 8 and 3.The TMSEt glycoside of the terminal trisaccharide was converted, via the 1-acetate, into the corresponding isobutyl (4) and 3-butylsulfonyl-2-propyl (5) glycosides and into the TMSEt thioglycoside 6 via the glycosyl bromide.

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