2-Chloro-4-nitrophenyl-2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranoside is a chemical compound that belongs to the class of glycosides, specifically a glucoside derivative. This compound features a glucopyranoside moiety, which is a six-membered cyclic form of glucose, acetylated at four hydroxyl groups, enhancing its stability and lipophilicity. The presence of a chloro and a nitro group on the aromatic ring contributes to its reactivity and potential applications in organic synthesis. The acetyl groups can be hydrolyzed under basic or enzymatic conditions, releasing the parent glucopyranoside. This compound may be utilized in various fields, including medicinal chemistry and biochemistry, particularly in studies involving glycosylation reactions or as a substrate for glycosidases. Its specific properties, such as solubility, melting point, and reactivity, would depend on the solvent and conditions used in experiments. As with many chemical substances, appropriate safety measures should be taken when handling this compound due to its potential toxicity and reactivity.

2-CHLORO-4-NITROPHENYL-2,3,4,6-TETRA-O-ACETYL-ALPHA-D-GLUCOPYRANOSIDE

153823-58-6: 2-Chloro-4-nitrophenyl-2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranoside is a chemical compound that belongs to the class of glycosides, specifically a glucoside derivative. This compound features a glucopyranoside moiety, which is a six-membered cyclic form of glucose, acetylated at four hydroxyl groups, enhancing its stability and lipophilicity. The presence of a chloro and a nitro group on the aromatic ring contributes to its reactivity and potential applications in organic synthesis. The acetyl groups can be hydrolyzed under basic or enzymatic conditions, releasing the parent glucopyranoside. This compound may be utilized in various fields, including medicinal chemistry and biochemistry, particularly in studies involving glycosylation reactions or as a substrate for glycosidases. Its specific properties, such as solubility, melting point, and reactivity, would depend on the solvent and conditions used in experiments. As with many chemical substances, appropriate safety measures should be taken when handling this compound due to its potential toxicity and reactivity.

2-Chloro-4-nitrophenyl-2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside

2-Chloro-4-nitrophenyl 2,3,4,6-tetra-O-acetyl-a-D-glucopyranoside is a chromogenic substrate used to characterize enzymes in biochemical assays. The substrate is cleaved by enzymes, such as esterases and glycosidases, releasing the chromogenic group, which can be detected by its yellow color.

CAS 153823-58-6

2-CHLORO-4-NITROPHENYL-2,3,4,6-TETRA-O-ACETYL-ALPHA-D-GLUCOPYRANOSIDE

2-Chloro-4-nitrophenyl-2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside

Ref: 7W-GC3725

2-Chloro-4-nitrophenyl 2,3,4,6-tetra-O-acetyl-a-D-glucopyranoside

Ref: 3D-EC06599