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O-(6-O-acetyl-2,3,4-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-6-O-acetyl-2,3-di-O-benzyl-D-galactopyranosylfluoride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135503-34-3

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135503-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135503-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,5,0 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 135503-34:
(8*1)+(7*3)+(6*5)+(5*5)+(4*0)+(3*3)+(2*3)+(1*4)=103
103 % 10 = 3
So 135503-34-3 is a valid CAS Registry Number.

135503-34-3Relevant academic research and scientific papers

Synthesis of (1----4)-linked galacturonic acid trisaccharides, a proposed plant wound-hormone and a stereoisomer.

Nakahara,Ogawa

, p. 363 - 375 (2007/10/02)

Syntheses of alpha-GalA-(1----4)-alpha-GalA-(1----4)-GalA, a proposed plant wound-hormone, and its stereoisomer beta-GalA-(1----4)-alpha-GalA-(1----4)-GalA are described. The key intermediates, tert-butyldiphenylsilyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-alpha-D-galactopyranosyl)-(1----4)-O-(6 -O- acetyl-2,3-di-O-benzyl-alpha-D-galactopyranosyl)-(1----4)-6-O-acetyl-2,3 -di-O- benzyl-beta-D-galactopyranoside and tert-butyldiphenylsilyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-beta-D-galactopyranosyl)-(1----4)-O-(6- O- acetyl-2,3-di-O-benzyl-alpha-D-galactopyranosyl)-(1----4)-6-O-acetyl-2,3 -di-O- benzyl-beta-D-galactopyranoside, were prepared by stereoselective alpha-glycosylation of tert-butyldiphenylsilyl 6-O-acetyl-2,3-di-O-benzyl-beta-D-galactopyranoside with O-(6-O-acetyl-2,3,4-tri-O-benzyl-alpha-D-galactopyranosyl)-(1----4)-6-O- acetyl-2,3-di-O-benzyl-D-galactopyranosyl fluoride and O-(6-O-acetyl-2,3,4-tri-O-benzyl-beta-D-galactopyranosyl)-(1----4)-6-O-a cetyl- 2,3-di-O-benzyl-D-galactopyranosyl fluoride, respectively. The corresponding beta isomers were minor products. Characteristic features in the n.m.r. data of the key intermediates are discussed.

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