2,4,6-Tribromophenyl b-D-Glucopyranoside

• CAT Number: C000747
• CAS Number: 502495-87-6
• Molecular Formula: C₁₂H₁₃Br₃O₆
• Molecular Weight: 492.94
• Purity: ≥95%
• Solubility: DMSO (Slightly), Methanol (Slightly)
• Appearance: White to Off-White Solid
• Storage: 4°C
• IUPAC Name: (2S,3R,4R,5S,6R)-2-(hydroxymethyl)-6-(2,4,6-tribromophenoxy)oxane-3,4,5-triol
• InChI: InChI=1S/C12H13Br3O6/c13-4-1-5(14)11(6(15)2-4)21-12-10(19)9(18)8(17)7(3-16)20-12/h1-2,7-10,12,16-19H,3H2/t7-,8-,9+,10-,12+/m0/s1
• InChIKey: OLINLHROZJEXTO-GOVZDWNOSA-N
• SMILES: C1=C(C=C(C(=C1Br)OC2C(C(C(C(O2)CO)O)O)O)Br)Br

2,4,6-Tribromophenyl β-D-Glucopyranoside (Cat No.:C000747) is a chemical compound composed of a β-D-glucopyranoside moiety attached to a phenyl ring that bears three bromine substituents at the 2, 4, and 6 positions. This compound is likely of interest in fields like carbohydrate chemistry and chemical biology. Its unique structure may enable its use as a glycosylation reagent or as a starting material for the synthesis of other carbohydrate derivatives. Research involving 2,4,6-Tribromophenyl β-D-Glucopyranoside may contribute to the development of new methods for glycosylation reactions or other applications in organic synthesis.

Reference

Ludovici, D. et al.: Bioorg. Med. Chem. Lett., 11, 2229, (2001); Hovander, L. et al.: Arch. Env. Cont. Toxicol., 42, 105 (2002);