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methyl O-(2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129796-72-1

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129796-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129796-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,9 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 129796-72:
(8*1)+(7*2)+(6*9)+(5*7)+(4*9)+(3*6)+(2*7)+(1*2)=181
181 % 10 = 1
So 129796-72-1 is a valid CAS Registry Number.

129796-72-1Downstream Products

129796-72-1Relevant articles and documents

Synthesis of β-D-ribofuranosyl-(1→3)-α-L-rhamnopyranose by in situ activating glycosylation using 1-OH sugar derivative and Me3SiBr-CoBr2-Bu4NBr-molecular sieves 4A system

Hirooka,Mori,Sasaki,Koto,Shinoda,Morinaga

, p. 1679 - 1694 (2007/10/03)

Β-D-Ribofuranosyl-(1→3)-α-L-rhamnopyranosyl-(1→3)- L-rhamnopyranose, the trisaccharide repeating unit of the C. freundii O28, 1c O-specific polysaccharide, was synthesized using in situ activating glycosylation of the 1-OH sugar derivatives and a reagent mixture of trimethylsilyl bromide, cobalt(II) bromide, tetrabutylammonium bromide, and molecular sieves 4A. Regioselective tritylation was useful for synthesizing the 3-OH derivatives of methyl, allyl, and benzyl α-L-rhamnosides.

α-Selective thermal glycosidation of rhamnosyl and mannosyl chlorides

Nishizawa, Mugio,Kan, Yukiko,Shimomoto, Waka,Yamada, Hidetoshi

, p. 2431 - 2434 (2007/10/02)

Stereoselective thermal glycosylation of a variety of alcohols with 2,3,4-tri-O-benzylα-L-rhamnopyranosyl chloride and 2,3,4,6-tstra-O-benzyl-α-D-mannopyranosyl chloride have achieved to give α-glycosides in high selectivity.

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