CAS 13242-51-8

Formula: C20H23NO12

InChI: InChI=1S/C20H23NO12/c1-10(22)28-9-16-17(29-11(2)23)18(30-12(3)24)19(31-13(4)25)20(33-16)32-15-7-5-14(6-8-15)21(26)27/h5-8,16-20H,9H2,1-4H3/t16-,17-,18+,19+,20+/m1/s1

InChI key: BEUISCKWILNFIL-SLHNCBLASA-N

SMILES: CC(=O)OC[C@@H]1[C@H]([C@@H]([C@@H]([C@H](O1)OC2=CC=C(C=C2)[N+](=O)[O-])OC(=O)C)OC(=O)C)OC(=O)C

(2R,3R,4S,5S,6R)-2-(ACETOXYMETHYL)-6-(4-NITROPHENOXY)TETRAHYDRO-2H-PYRAN-3,4,5-TRIYL TRIACETATE

CAS: 13242-51-8

Formula: C₂₀H₂₃NO₁₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 469.3961

Ref: IN-DA0010OX

p-Nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside

CAS: 13242-51-8

p-Nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside is a biochemical reagent essential for glycobiology studies. Glycobiology focuses on the structure, synthesis, biology, and evolution of sugars, encompassing carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the roles of glycans in biological systems. This field is closely linked to fundamental research, biomedicine, and biotechnology.

Formula: C₂₀H₂₃NO₁₂

Color and Shape: Solid

Molecular weight: 469.4

Ref: TM-TSW-00377

4-Nitrophenyl 2,3,4,6-Tri-O-acetyl-α-D-mannopyranoside

CAS: 13242-51-8

Molecular weight: 469.40

Ref: 7W-GC8979

4-Nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside

CAS: 13242-51-8

4-Nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside

Formula: C₂₀H₂₃NO₁₂

Purity: 95%

Molecular weight: 469.39611

Ref: 54-BICL2486

4-Nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside

Controlled Product

CAS: 13242-51-8

Applications 4-Nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside (cas# 13242-51-8) is a compound useful in organic synthesis.

Formula: C₂₀H₂₃NO₁₂

Color and Shape: Neat

Molecular weight: 469.4

Ref: TR-N506780

4-Nitrophenyl 2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside

CAS: 13242-51-8

4-Nitrophenyl 2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside is a highly sensitive and efficient chromogenic substrate designed for the detection and quantification of α-D-mannosidases. These enzymes play a crucial role in the degradation and metabolism of glycoproteins and glycolipids, thus having high importance in biotechnology and biochemical research. When acted upon by α-D-mannosidase, this substrate releases a bright yellow product, 4-nitrophenol, which is easily measured spectrophotometrically at 405 nm. This enables quick and accurate analysis in various applications such as enzyme kinetics, inhibitor screening, and activity assays.

Purity: Min. 95%

Molecular weight: 469.4 g/mol

Ref: 3D-EN16817