CAS 35023-71-3

[(3R,4S,5S,6S)-3,4,5-triacetoxy-6-(2-chloro-4-nitro-phenoxy)tetrahydropyran-2-yl]methyl acetate

Description:

The chemical substance with the name "[(3R,4S,5S,6S)-3,4,5-triacetoxy-6-(2-chloro-4-nitro-phenoxy)tetrahydropyran-2-yl]methyl acetate" and CAS number 35023-71-3 is a complex organic compound characterized by its tetrahydropyran ring structure, which is a six-membered cyclic ether. This compound features multiple acetoxy groups, indicating the presence of acetyl functional groups that can influence its reactivity and solubility. The presence of a chloro and nitro substituent on the phenoxy group suggests potential biological activity, as such groups can enhance the compound's interaction with biological targets. The stereochemistry, denoted by the R and S configurations, indicates specific spatial arrangements of atoms, which can significantly affect the compound's properties and behavior in chemical reactions. Overall, this compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry and drug development. Its unique structural features contribute to its potential applications in various fields, including pharmaceuticals and agrochemicals.

Formula: C₂₀H₂₂ClNO₁₂

InChI: InChI=1/C20H22ClNO12/c1-9(23)29-8-16-17(30-10(2)24)18(31-11(3)25)19(32-12(4)26)20(34-16)33-15-6-5-13(22(27)28)7-14(15)21/h5-7,16-20H,8H2,1-4H3/t16?,17-,18+,19+,20-/m1/s1

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

CAS: 35023-71-3

Molecular weight: 503.84

Ref: 7W-GC2778

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

CAS: 35023-71-3

2-Chloro-4-nitrophenyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside is a chromogenic enzyme substrate used in the biochemical characterization of various enzymes. It produces a yellow color when cleaved by enzymes and is commonly used in assays to study enzyme kinetics and activity. It is commonly used is used to study the biochemical and physiological effects of glycosylation and acts as a substrate for glycosylation-dependent enzymes involved in carbohydrate metabolism. Glycosidases hydrolyse 2-Chloro-4-nitrophenyl-2,3,4,6-tetra-O-acetyl-beta-D-glucopyranoside, releasing 2-chloro-4-nitrophenyl moiety, and the substrate can then be further metabolized by other enzymes. It is also used in the investigate the effects and activity on glycoproteins and glycolipids.

Purity: Min. 95%

Molecular weight: 503.84 g/mol

Ref: 3D-EC03194