CAS 13089-23-1

4-Nitrophenyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside

Description:

4-Nitrophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyranoside is a synthetic compound that belongs to the class of glycosides, specifically a derivative of glucosamine. This compound features a glucopyranoside backbone, which is a six-membered cyclic structure derived from glucose, modified with an acetamido group and multiple acetyl groups at specific hydroxyl positions. The presence of the nitrophenyl group indicates that it has potential applications in biochemical assays, particularly as a substrate for glycosidase enzymes. The acetylation of hydroxyl groups enhances the compound's stability and solubility in organic solvents, making it useful in various chemical reactions and studies. Its structural complexity allows for specific interactions in biological systems, which can be exploited in research related to carbohydrate chemistry and enzyme kinetics. Overall, this compound serves as a valuable tool in the study of glycosylation processes and enzyme activity in biochemical research.

p-Nitrophenyl 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-glucopyranoside

CAS: 13089-23-1

Molecular weight: 468.41

Ref: 7W-GC2865

p-Nitrophenyl 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-glucopyranoside

Controlled Product

CAS: 13089-23-1

Applications p-Nitrophenyl 2-Acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-glucopyranoside (cas# 13089-23-1) is a compound useful in organic synthesis.

Formula: C₂₀H₂₄N₂O₁₁

Color and Shape: Neat

Molecular weight: 468.41

Ref: TR-N502095

4-Nitrophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside

CAS: 13089-23-1

4-Nitrophenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside is a synthetic compound with the ability to inhibit the enzyme glutamicum. It is a radionuclide that can be used as a focusing agent for gamma cameras and has been shown to be effective against corynebacterium glutamicum and other organisms. 4NP2AG was synthesized by reacting nitrophenol with acetamide in the presence of an acid catalyst and hydrogenating the product. The synthesis employs precession chemistry, which involves rotating a molecule around its axis at high speed to increase its concentration in one area. This treatment leads to a higher yield of desired product. 4NP2AG contains two acetamido groups on the glucopyranoside moiety, which are esterified with nitrophenol and acetic acid respectively. These moieties are

Purity: Min. 95%

Molecular weight: 468.41 g/mol

Ref: 3D-EN06131