CAS 57783-81-0
:Phenylmethyl 2,3,6-tris-O-(phenylmethyl)-β-D-galactopyranoside
Description:
Phenylmethyl 2,3,6-tris-O-(phenylmethyl)-β-D-galactopyranoside, with the CAS number 57783-81-0, is a glycoside compound derived from galactose. It features a galactopyranoside backbone, which is a six-membered cyclic form of galactose, substituted at the 2, 3, and 6 positions with phenylmethyl (benzyl) groups. This structure contributes to its solubility and reactivity, making it a useful compound in various biochemical applications. The presence of multiple phenylmethyl groups enhances its hydrophobic character, potentially influencing its interaction with biological membranes and proteins. This compound may exhibit specific biological activities, such as enzyme inhibition or modulation of cellular processes, due to its glycosidic nature. Additionally, it can serve as a substrate or inhibitor in glycosylation reactions, making it relevant in the study of carbohydrate chemistry and biochemistry. Its synthesis and characterization are of interest in the field of medicinal chemistry, particularly for the development of glycosylated drugs or probes for biological research.
Formula:C34H36O6
InChI:InChI=1S/C34H36O6/c35-31-30(25-36-21-26-13-5-1-6-14-26)40-34(39-24-29-19-11-4-12-20-29)33(38-23-28-17-9-3-10-18-28)32(31)37-22-27-15-7-2-8-16-27/h1-20,30-35H,21-25H2/t30-,31+,32+,33-,34-/m1/s1
InChI key:InChIKey=HYZRJGYIUDQFSY-BWNLSPMZSA-N
SMILES:O(CC1=CC=CC=C1)[C@@H]2[C@@H](OCC3=CC=CC=C3)[C@@H](O)[C@@H](COCC4=CC=CC=C4)O[C@H]2OCC5=CC=CC=C5
Synonyms:- β-D-Galactopyranoside, phenylmethyl 2,3,6-tris-O-(phenylmethyl)-
- Phenylmethyl 2,3,6-tris-O-(phenylmethyl)-β-D-galactopyranoside
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Found 3 products.
Benzyl 2,3,6-Tri-O-benzyl-β-D-galactopyranoside
CAS:Controlled ProductFormula:C34H36O6Color and Shape:NeatMolecular weight:540.651,2,3,6-Tetra-O-benzyl-b-D-galactopyranoside
CAS:<p>The chemical structure of 1,2,3,6-Tetra-O-benzyl-b-D-galactopyranoside is the product of a custom synthesis. It is a synthetic oligosaccharide with a high purity and high degree of methylation. The chemical modification includes fluorination and glycosylation. This compound has been shown to have potent anti-tuberculosis activity in vitro and in vivo.</p>Formula:C34H36O6Purity:Min. 95%Molecular weight:540.65 g/mol


