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Methyl 2,3,6-tri-O-benzoyl-alpha-D-mannopyranoside is a complex organic compound that belongs to the class of glycosides, specifically a derivative of alpha-D-mannopyranose, a monosaccharide. Methyl 2,3,6-tri-O-benzoyl-alpha-D-mannopyranoside is characterized by the presence of three benzoyl groups attached to the 2nd, 3rd, and 6th carbon atoms of the mannopyranose ring, with a methyl group at the anomeric carbon (1st carbon). The benzoyl groups serve as protecting groups, which are commonly used in organic synthesis to prevent unwanted reactions at specific hydroxyl groups. Methyl 2,3,6-tri-O-benzoyl-alpha-D-mannopyranoside is of interest in the field of carbohydrate chemistry, particularly in the synthesis of more complex oligosaccharides and polysaccharides, as well as in the study of enzyme interactions with carbohydrates.

3396-68-7

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3396-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3396-68-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,9 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3396-68:
(6*3)+(5*3)+(4*9)+(3*6)+(2*6)+(1*8)=107
107 % 10 = 7
So 3396-68-7 is a valid CAS Registry Number.

3396-68-7Relevant academic research and scientific papers

Synthesis of pentasaccharide and heptasaccharide derivatives and their effects on plant growth

Liu, Hongmei,Cheng, Shuihong,Liu, Jun,Du, Yuguang,Bai, Zhihui,Du, Yuguo

scheme or table, p. 5634 - 5638 (2010/03/30)

Two oligosaccharide derivatives, β-D-Glcp-(1-6)-β-D-Glcp-(1-6)- β-D-Glcp-(1-6)-β-D-Glcp-(1-4)-α-D-ManpOMe (1) and β-D-Glcp-(1-6)-β-D-Glcp-(1-6)-β-D-Glcp-(1-6)-β-D-Glcp-(1-6) -β-D-Glcp-(1-6)-β-D-Glcp-(1-4)-α-D-ManpOMe (2), have been synthesized efficiently using a convergent glycosylation strategy of 2 + 3 and 2 + 5.1,6-Anhydro-β-D-glucopyranose, which was prepared from cotton pyrolysis, was applied as a key synthon in the synthesis, significantly simplifying the preparation. The bioassay suggested that these two oligosaccharides can both stimulate the growth of maize cultured in liquid medium at a concentration of 3 ppm.

Synthesis of the C-linked disaccharide α-D-man-(1→4)-D-man employing a SmI2-mediated C-glycosylation step: En route to cyclic C-oligosaccharides

Mikkelsen, Lise Munch,Skrydstrup, Troels

, p. 2123 - 2128 (2007/10/03)

Investigations are reported on the assembly of the C-linked disaccharide α-D-Man-(1→4)-D-Man, representing the first steps in our projected synthesis of a cyclic C-oligomer containing repeating units of this C-dimer. The key step in this synthesis uses a

Regioselective benzoylation of sugars mediated by excessive Bu2SnO: Observation of temperature promoted migration

Zhang, Zhiyuan,Wong, Chi-Huey

, p. 6513 - 6519 (2007/10/03)

Regioselective benzoylation of carbohydrates using an excess of dibutyltin oxide (Bu2SnO) at increased reaction temperatures has been developed for the synthesis of several glycoside benzoates with one or two free hydroxyl groups, including gal

Parasite glycoconjugates. Part 6. Chemical synthesis of phosphorylated penta- and hepta-saccharide fragments of Leishmania major antigenic lipophosphoglycan

Nikolaev, Andrei V.,Watt, Gregory M.,Ferguson, Michael A. J.,Brimacombe, John S.

, p. 969 - 979 (2007/10/03)

The phosphorylated branched oligosaccharides 1 and 2, fragments of the phosphoglycan portion of Leishmania major lipophosphoglycan, have been synthesized using the trichloroacetimidate method for the glycosylation reactions and the phosphoramidite and hydrogenphosphonate methods for phosphorylation.

Synthesis of mono- and dimannoside phosphoramidite derivatives for solid-phase conjugation to oligonucleotides

Akhtar,Akhtar, Saghir,Routledge,Routledge, Anne,Patel,Patel, Ramila,Gardiner,Gardiner, John M.

, p. 7333 - 7336 (2007/10/02)

Mannose and dimannose derivatives have been prepared with an anomerically-linked hydrophobic spacer, and converted to phoshoramidite derivatives suitable for conjugation to oligoribodeoxynucleotides on a DNA/RNA synthesizer. Synthesis of a monomannoside-linked 15-mer oligoribodeoxynucleotide is reported.

Oxidative Cleavage of 4,6-O-Benzylidene Ring with t-Butyl Hydroperoxide and Copper(II) Chloride. Preparation of Methyl 4-O- and 6-O-Benzoylhexopyranoside Derivatives

Sato, Ken-ichi,Igarashi, Tetsutaro,Yanagisawa, Yukio,Kawauchi, Nobuya,Hashimoto, Hironobu,Yoshimura, Juji

, p. 1699 - 1702 (2007/10/02)

Copper(II) chloride and palladium(II) acetate were found to be highly effective catalysts for oxidative cleavage of O-benzylidene ring with t-butyl hydroperoxide.Using the former catalyst 4,6-O-benzylidenehexopyranoside derivatives were converted into the

Dioxolanylium Ions Derived from Carbohydrates. IX. Rearrangement between Dioxolanylium and Dioxanylium Ions

Jacobsen, Steffen

, p. 157 - 164 (2007/10/02)

The formation of 4,6-acetoxonium and benzoxonium ion derivatives of methyl gluco-, manno-, galacto- and idopyranosides from the 6-azido-6-deoxy compounds on treatment with nitrosonium ion is described and the formation and rearrangement of the 3,5-benzoxonium ion derived from methyl α-d-xylofuranoside discussed.

REGIOSELECTIVE O-DEACYLATION OF FULLY ACYLATED GLYCOSIDES AND 1,2-O-ISOPORPYLIDENEALDOFURANOSE DERIVATIVES WITH HYDRAZINE HYDRATE

Ishido, Yoshiharu,Sakairi, Nobuo,Sekiya, Masao,Nakazaki, Nobuo

, p. 51 - 80 (2007/10/02)

On hydrazinolyis in 1:4 acetic acid-pyridine, and in pyridine, partisl O-deacylation of fully acylated methyl glycosides and some other glycosyl compounds ( 23 compounds ) was found to be induced, to give, in good yields, products bearing one free hydroxy

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