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methyl 3,4-di-O-benzyl-α-D-xylopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81307-68-8

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81307-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81307-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,0 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81307-68:
(7*8)+(6*1)+(5*3)+(4*0)+(3*7)+(2*6)+(1*8)=118
118 % 10 = 8
So 81307-68-8 is a valid CAS Registry Number.

81307-68-8Relevant academic research and scientific papers

Total synthesis and structural revision of the presumed aeruginosins 205A and B

Hanessian, Stephen,Wang, Xiaotian,Ersmark, Karolina,Del Valle, Juan R.,Klegraf, Ellen

supporting information; experimental part, p. 4232 - 4235 (2009/12/30)

A stereoselective synthesis of enantiopure aeruginosin 205B aglycon confirms the presence of a (3R,2S)-3-chloroleucine amide residue and a (6R)-hydroxy (4aR,7aS)-octahydroindole-(2S)-2-carboxamide (Choi) subunit instead of a 6-chloro-substituted core (Cco

Oligosaccharides related to xyloglucan: synthesis and X-ray crystal structure of methyl alpha-L-fucopyranosyl-(1-->2)-beta-D-galactopyranosyl-(1-->2)-alpha-D-x ylopyranoside and the synthesis of methyl alpha-L-fucopyranosyl-(1-->2)-beta-D-galactopyranosyl

Watt,Brasch,Larsen,Melton,Simpson

, p. 300 - 312 (2007/10/03)

Trisaccharides, methyl alpha-L-fucopyranosyl-(1-->2)-beta-D-galactopyranosyl-(1-->2)-alpha-D-xy lopyranoside and methyl alpha-L-fucopyranosyl-(1-->2)-beta-D-galactopyranosyl-(1-->2)-beta-D-xyl opyranoside, which are related to the side chain of xyloglucan

The Direct Synthesis of Methyl 2,4-Di-O-benzyl-α-D-xylopyranoside by the Regiospecific Benzylation of Methyl α-D-Xylopyranoside

Morishima, Naohiko,Koto, Shinkiti,Kusuhara, Chiharu,Zen, Shonosuke

, p. 631 - 632 (2007/10/02)

The regiospecific benzylation of methyl α-D-xylopyranoside with benzyl chloride and sodium hydride produces methyl 2,4-di-O-benzyl-α-D-xylopyranoside in a 70percent yield, together with the by-products, methyl 2,3- and 3,4-di-O-benzyl-α-D-xylopyranosides.The structure of the 2,4-di-O-benzyl derivative was confirmed through the alternative synthesis of the 2,3- and 3,4-di-O-benzyl derivatives via the O-isopropylidene and O-cyclohexylidene derivatives of methyl α-D-xylopyranoside.

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