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Methyl 2,3-di-O-benzoyl-6-deoxy-4-O-(p-tolylsulfonyl)-α-D-glucopyranoside is a complex organic compound with the molecular formula C27H28O9S. It is a derivative of α-D-glucopyranoside, a monosaccharide, with modifications at the 2,3, and 6 positions. Specifically, the 2 and 3 positions are each substituted with a benzoyl group, while the 6 position is deoxygenated. Additionally, the 4 position is substituted with a p-tolylsulfonyl group, which introduces a toluene sulfonate moiety. methyl 2,3-di-O-benzoyl-6-deoxy-4-O-(p-tolylsulfonyl)-α-D-glucopyranoside is significant in organic chemistry, particularly in the synthesis of complex carbohydrates and as a potential intermediate in the preparation of pharmaceuticals and other bioactive molecules. Its structure provides a platform for further functionalization and modification, making it a valuable building block in the field of carbohydrate chemistry.

6893-93-2

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6893-93-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6893-93-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,9 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6893-93:
(6*6)+(5*8)+(4*9)+(3*3)+(2*9)+(1*3)=142
142 % 10 = 2
So 6893-93-2 is a valid CAS Registry Number.

6893-93-2Downstream Products

6893-93-2Relevant academic research and scientific papers

Synthesis of furanoid and pyranoid derivatives of 6-deoxy-4-thio-D-galactose

Cicero, Daniel,Varela, Oscar,De Lederkremer, Rosa M.

, p. 1131 - 1144 (2007/10/02)

The synthesis of pyranoid and furanoid derivatives of 6-deoxy-4-thio-D-galactose from methyl α-D-glucopyranoside (1) is described. A key intermediate for the synthesis, methyl 2,3-di-O-benzoyl-6-deoxy-4-thio-α-D-galactopyranoside (15) was prepared by diff

SYNTHESIS OF STEREOSPECIFICALLY LABELED CARBOHYDRATES II: PREPARATION OF (3S)- AND (3R)-ABEQUOSE

Weigel, Theresa M.,Liu, Hung-wen

, p. 4221 - 4224 (2007/10/02)

Preparation of methyl 3,6-dideoxy-D-xylo-hexapyranoside (methyl abequoside) having deuterium stereospecifically labeled at the 3S (1) and 3R (2) position, respectively, via three different routes is described.

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