(2R,3R,4S,5R,6R)-2-[(6-bromonaphthalen-2-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

• ChemBase ID: 103080
• Molecular Formular: C16H17BrO6
• Molecular Mass: 385.20658
• Monoisotopic Mass: 384.02085026
• SMILES: Brc1ccc2cc(O[C@H]3O[C@@H]([C@H](O)[C@H](O)[C@H]3O)CO)ccc2c1
• Canonical SMILES: OC[C@H]1O[C@H](Oc2ccc3c(c2)ccc(c3)Br)[C@@H]([C@H]([C@H]1O)O)O
• InChI: InChI=1S/C16H17BrO6/c17-10-3-1-9-6-11(4-2-8(9)5-10)22-16-15(21)14(20)13(19)12(7-18)23-16/h1-6,12-16,18-21H,7H2/t12-,13+,14+,15-,16+/m1/s1
• InChIKey: NLRXQZJJCPRATR-CWVYHPPDSA-N

NAMES AND DATABASE IDS

Names

• IUPAC name: (2R,3R,4S,5R,6R)-2-[(6-bromonaphthalen-2-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
• IUPAC Traditional name: (2R,3R,4S,5R,6R)-2-[(6-bromonaphthalen-2-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
• Synonyms: 6-BROMO-2-NAPHTHYL-α-D-GALACTOPYRANOSIDE

Database IDs

• CAS Number: 25997-59-5
• EC Number: 247-398-4
• PubChem SID: 162090186
• PubChem CID: 117705

CALCULATED PROPERTIES

• Acid pKa: 12.200141
• H Acceptors: 6
• H Donor: 4
• LogD (pH = 5.5): 1.1598417
• LogD (pH = 7.4): 1.1598349
• Log P: 1.1598418
• Molar Refractivity: 84.2563 cm^3
• Polarizability: 34.84967 Å^3
• Polar Surface Area: 99.38 Å^2
• Rotatable Bonds: 3
• Lipinski's Rule of Five: true

PROPERTIES

Safety Information

• Storage Condition: 2-8°C, Desiccate, Protect from light

DETAILS

MP Biomedicals - 02150520

Crystalline
Chromogenic substrate for
α-galactosidase