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benzyl O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-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.

62867-79-2

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62867-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62867-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,6 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62867-79:
(7*6)+(6*2)+(5*8)+(4*6)+(3*7)+(2*7)+(1*9)=162
162 % 10 = 2
So 62867-79-2 is a valid CAS Registry Number.

62867-79-2Relevant academic research and scientific papers

Synthesis of Globotriaosylceramide (Gb3) and Isoglobotriaosylceramide (isoGb3)

Qiu, Dongxu,Schmidt, Richard R.

, p. 217 - 224 (2007/10/02)

The synthesis of globotriaosylceramide (1) was based on O-galactosyl trichloroacetimidate 5α as donor and 4b-O-unprotected lactose 7 as acceptor; 7 was readily accessible from lactose.Glycosylation by an "inverted procedure" afforded preferentially the α-

Glycosyl Imidates, 42.- Selectively Protected Lactose and 2-Azido Lactose, Building Blocks for Glycolipid Synthesis

Jung, Karl-Heinz,Hoch, Monika,Schmidt, Richard R.

, p. 1099 - 1106 (2007/10/02)

Performing regioselective alkylation at 3'-OH of benzyl β-lactoside 1 by the stannylation method we prepared the 3'-OH- and 4'-OH-unprotected lactose derivatives 5 and 10 and the 4'-OH-unprotected lactose derivative 9 containing a different protecting gro

Total synthesis of globotriaosyl-E and Z-ceramides and isoglobotriaosyl-E-ceramide.

Koike,Sugimoto,Sato,Ito,Nakahara,Ogawa

, p. 189 - 208 (2007/10/02)

Stereoselective, total synthesis of O-alpha-D-galactopyranosyl-(1----4) -O-beta-D-galactopyranosyl-(1----4)-O-beta-D-glucopyranosyl-(1----1)-N -tetracosanoyl-[2S,3R,4E (and 4Z)]-sphingenine and O-alpha-D -galactopyranosyl-(1----3)-O-beta-D-galactopyranosyl-(1----4)-O-beta-D -glucopyranosyl-(1----1)-N-tetracosanoyl-(2S,3R,4E)-sphin gen ine was achieved by using O-(2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranosyl) -(1----4)-O-(2,3,6-tri-O-acetyl-beta-D-galactopyranosyl)-(1----4)-2,3,6- tri-O-acetyl-alpha-D-glucopyranosyl trichloroacetimidate, O-(2,3,4,6-tetra-O-acetyl-alpha-D-galactopyranosyl) -(1----4)-O-(2,3,6-tri-O-acetyl-beta-D-galactopyranosyl)-(1----4)-2,3,6- tri-O-acetyl-alpha (and beta)-D-glucopyranosyl fluoride, and O-(2,3,4,6-tetra-O-acetyl-alpha-D -galactopyranosyl)-(1----3)-O-(2,3,6-tri-O-acetyl-beta-D-galactopyran osyl)-(1----4)-2,3,6-tri-O-acetyl-alpha-D-glucopyranosyl trichloroacetimidate.

Building Units of Oligosaccharides, XXXVI. - Investigation of Reactivity in Tri-and Pentasaccharide Syntheses. Improved Synthesis of the Pentasaccharide Chain of the Forssman Antigen

Paulsen, Hans,Buensch, Almuth

, p. 2204 - 2215 (2007/10/02)

The dependence of selectivity and yield upon the initial saccharide's reactivity is shown for the syntheses of the trisaccharides 7, 8, 9, and 12.From 8 comes the trisaccharide halide 15 which, together with 22 in a block synthesis, yields the pentasaccha

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