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benzyl 2,3,4-tri-O-acetyl-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29868-41-5

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29868-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29868-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,6 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29868-41:
(7*2)+(6*9)+(5*8)+(4*6)+(3*8)+(2*4)+(1*1)=165
165 % 10 = 5
So 29868-41-5 is a valid CAS Registry Number.

29868-41-5Relevant academic research and scientific papers

Chemoenzymatic synthesis of naturally occurring benzyl 6-O-glycosyl-β- D-glucopyranosides

Kawahara, Eiji,Fujii, Mikio,Kato, Keisuke,Ida, Yoshiteru,Akita, Hiroyuki

, p. 1058 - 1061 (2007/10/03)

Direct β-glucosidation between benzyl alcohol and D-glucose (5) using the immobilized β-glucosidase from almonds with the synthetic prepolymer ENTP-4000 gave a benzyl β-D-glucoside (1) in 53% yield. The coupling of the benzyl β-D-glucopyranoside congener

Synthesis of Ganglioside M5 from Sea Urchin Egg

Yamamoto, Toshihiro,Teshima, Tadashi,Saitoh, Umihito,Hoshi, Motonori,Shiba, Tetsuo

, p. 2701 - 2704 (2007/10/02)

A main component of ganglioside M5 from egg of the sea urchin, Anthocidaris crassispina, Neu5Gcα2->6Glcβ1->1Cer (1), which has N-glycolyl group in neuraminic acid part, as well as phytosphingosine and saturated nonhydroxy fatty acid in ceramide part was f

Syntheses of Benzyl 6-O-Sulfo-β-D-glucopyranoside Salts and Their 6S-Deuterated Analogues. Conformational Preferences of Their (Sulfonyloxy)methyl Group

Meyer, Bernd,Stuike-Prill, Rainer

, p. 902 - 906 (2007/10/02)

The syntheses of benzyl 6-O-sulfo-β-D-glucopyranoside as the sodium (7), lithium (8), potassium (9), and calcium (10) salts in 30percent total yield from D-glucose are described.Sulfation of the 6-hydroxy compounds 5 and 17 involved quenching of the react

A New Method for Cleaving Carbohydrate Triphenylmethyl and Benzyl Ethers

Klemer, Almuth,Bieber, Michael,Wilbers, Hubert

, p. 1416 - 1421 (2007/10/02)

Carbohydrate triphenylmethyl and benzyl ethers are converted into their trimethylsilyl ethers by iodotrimethylsilane.The silyl ethers are hydrolysed to give partially free sugars.From multiple benzylated glycosides it is possible to remove selectively the primary benzyl group, under more vigorous conditions total debenzylation occurs.

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