CAS 77640-21-2

4-nitrophenyl 2-O-(6-deoxyhexopyranosyl)hexopyranoside

Description:

4-Nitrophenyl 2-O-(6-deoxyhexopyranosyl)hexopyranoside is a glycoside compound characterized by the presence of a nitrophenyl group and a sugar moiety. The structure features a 4-nitrophenyl group, which is known for its electron-withdrawing properties due to the nitro group, enhancing the compound's reactivity in various chemical reactions. The sugar component is a hexopyranoside, indicating that it is derived from a six-membered pyranose ring, and the presence of a 6-deoxy sugar suggests that one hydroxyl group has been replaced by a hydrogen atom, which can influence the compound's solubility and biological activity. This compound may exhibit specific interactions in biochemical pathways, making it of interest in fields such as medicinal chemistry and biochemistry. Its CAS number, 77640-21-2, allows for easy identification in chemical databases. Overall, the unique combination of functional groups in this compound contributes to its potential applications in research and industry.

Formula: C₁₈H₂₅NO₁₂

InChI: InChI=1/C18H25NO12/c1-7-11(21)13(23)15(25)17(28-7)31-16-14(24)12(22)10(6-20)30-18(16)29-9-4-2-8(3-5-9)19(26)27/h2-5,7,10-18,20-25H,6H2,1H3

SMILES: CC1C(C(C(C(O1)OC1C(C(C(CO)OC1Oc1ccc(cc1)N(=O)=O)O)O)O)O)O

4-Nitrophenyl 2-O-(b-L-fucopyranosyl)-b-D-galactopyranoside

CAS: 77640-21-2

Ref: 7W-GC7934

p-Nitrophenyl 2-O-(β-L-Fucopyranosyl)-β-D-galactopyranoside

Controlled Product

CAS: 77640-21-2

Applications A synthetic chromogenic substrate for the assay of α-fucosidases.
References DiCioccio, R.A., et al.: Anal. Biochem., 11, 176 (1981)

Formula: C₁₈H₂₅NO₁₂

Color and Shape: Neat

Molecular weight: 447.39

Ref: TR-N503558

4-Nitrophenyl 2-O-(b-L-fucopyranosyl)-b-D-galactopyranoside

CAS: 77640-21-2

4-Nitrophenyl 2-O-(b-L-fucopyranosyl)-b-D-galactopyranoside is a high-quality chromogenic substrate with excellent sensitivity specifically designed for enzymes' activity detection. This pNP substrate enables rapid, accurate, and measurable colorimetric visualization of enzymatic hydrolysis reactions. Researchers can easily and effectively monitor the release of 4-nitrophenol as a yellow product under laboratory conditions, allowing for convenient comparative analysis and identification of enzyme levels in various samples.

Purity: Min. 95%

Color and Shape: White Solid

Molecular weight: 447.39 g/mol

Ref: 3D-EN04839