CAS 7473-38-3

Phenylmethyl β-L-arabinopyranoside

Description:

Phenylmethyl β-L-arabinopyranoside, also known as phenylmethyl β-L-arabinofuranoside, is a glycoside derived from the sugar arabinose. It features a phenylmethyl (benzyl) group attached to the anomeric carbon of the arabinopyranose moiety, which contributes to its structural and functional properties. This compound is typically a white to off-white solid and is soluble in polar organic solvents, such as methanol and ethanol, but may have limited solubility in non-polar solvents. It is often used in biochemical research, particularly in studies involving carbohydrate interactions, enzyme activity, and as a potential substrate for glycosyltransferases. The presence of the phenylmethyl group can enhance the compound's stability and influence its biological activity. As with many glycosides, it may exhibit varying degrees of sweetness and can be involved in various metabolic pathways. Safety data should be consulted for handling and usage, as with any chemical substance.

Formula: C₁₂H₁₆O₅

InChI: InChI=1S/C12H16O5/c13-9-7-17-12(11(15)10(9)14)16-6-8-4-2-1-3-5-8/h1-5,9-15H,6-7H2/t9-,10-,11+,12-/m0/s1

InChI key: InChIKey=XUGMDBJXWCFLRQ-YFKTTZPYSA-N

SMILES: O(CC1=CC=CC=C1)[C@@H]2[C@H](O)[C@@H](O)[C@@H](O)CO2

Synonyms:

• β-L-Arabinopyranoside, phenylmethyl
• Phenylmethyl β-L-arabinopyranoside
• Benzyl β-L-arabinopyranoside
• Arabinopyranoside, benzyl, β-L-
• NSC 400277

Benzyl β-L-arabinopyranoside

CAS: 7473-38-3

Benzyl β-L-arabinopyranoside is a Glycosylation, complex carbohydrate, Methylation, Click modification, Polysaccharide, Fluorination, CAS No. 7473-38-3 that can be synthesized in the lab and is available for custom synthesis. It is used in the synthesis of saccharides and other glycosylated natural products.

Formula: C₁₂H₁₆O₅

Purity: (%) Min. 98%

Color and Shape: White Off-White Powder

Molecular weight: 240.25 g/mol

Ref: 3D-MB05959