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Triphenylmethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-thio-β-D-glucopyranoside is a complex organic compound with the molecular formula C36H37NO8S. It is a derivative of a sugar molecule, specifically a thio-glycoside, where the oxygen atom in the glycosidic linkage has been replaced by a sulfur atom. The compound features a triphenylmethyl group, which is a phenyl group (a benzene ring) attached to three methyl groups, providing steric hindrance and stability. The 2-acetamido group indicates the presence of an acetamide group at the second carbon position, while the 3,4,6-tri-O-acetyl groups signify the acetylation of the hydroxyl groups at the third, fourth, and sixth carbon positions. triphenylmethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-thio-β-D-glucopyranoside is of interest in the field of carbohydrate chemistry and may have applications in the synthesis of complex glycoconjugates and as a potential intermediate in the preparation of biologically active molecules.

91288-33-4

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91288-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91288-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,8 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91288-33:
(7*9)+(6*1)+(5*2)+(4*8)+(3*8)+(2*3)+(1*3)=144
144 % 10 = 4
So 91288-33-4 is a valid CAS Registry Number.

91288-33-4Relevant academic research and scientific papers

Combining Click Reactions for the One-Pot Synthesis of Modular Biomolecule Mimetics

Brink?, Anne,Risinger, Christian,Lambert, Annie,Blixt, Ola,Grandjean, Cyrille,Jensen, Henrik H.

supporting information, p. 7544 - 7548 (2019/10/08)

Here, we report on the first combined one-pot use of the two so-called "click reactions": The thiol-ene coupling and the copper-catalyzed alkyne-azide cycloaddition. These reactions were employed in an alternating and one-pot fashion to combine appropriately functionalized monomeric carbohydrate building blocks to create mimics of trisaccharides and tetrasaccharides as single anomers, with only minimal purification necessary. The deprotected oligosaccharide mimics were found to bind both plant lectins and human galectin-3.

S-, N-, and O-glycosyl derivatives of 2-acetamido-2-deoxy-D-glucose with hydrophobic aglycons as potential chemotherapeutic agents and N-acetyl-beta-D-glucosaminidase inhibitors.

Paul,Korytnyk

, p. 27 - 43 (2007/10/02)

S-, N-, and O-Glycosyl derivatives of 2-acetamido-2-deoxy-D-glucose with hydrophobic aglycons have been obtained as potential, plasma-membrane active agents. 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-thio-beta-D-glucopyranose (6) was converted into benzyl,

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