51349-63-4 , Naphthol AS-BI b-D-galactopyranoside

51349-63-4 , Naphthol AS-BI b-D-galactopyranoside;
7-Bromo-3-(b-D-galactopyranosyloxy)-N-(2-methoxyphenyl)-2-naphthalenecarboxamide,
Cas:51349-63-4
C24H24BrNO8 / 534.35
MFCD00076133

7-Bromo-3-(b-D-galactopyranosyloxy)-N-(2-methoxyphenyl)-2-naphthalenecarboxamide

Naphthol AS-BI b-D-galactopyranoside

Naphthol AS-BI b-D-galactopyranoside is a naphthol derivate that hydrolyzes to form indolyl. It has been shown to inhibit β-galactosidase activity in mice by competitive inhibition, and it has also been shown to be a coupling agent for the synthesis of beta-naphthol derivatives. Naphthol AS-BI b-D-galactopyranoside can be used in freeze dried organs as a coupling agent for the synthesis of indolyl derivatives.

Naphthol AS-BI beta-D-galactopyranoside is a synthetic compound that has gained significant attention from researchers in various fields of study. This compound is widely used in scientific experiments due to its unique physical and chemical properties.

CAS Number	51349-63-4
Product Name	Naphthol AS-BI beta-D-galactopyranoside
IUPAC Name	7-bromo-N-(2-methoxyphenyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalene-2-carboxamide
Molecular Formula	C24H24BrNO8
Molecular Weight	534.35 g/mol
InChI	InChI=1S/C24H24BrNO8/c1-32-17-5-3-2-4-16(17)26-23(31)15-9-13-8-14(25)7-6-12(13)10-18(15)33-24-22(30)21(29)20(28)19(11-27)34-24/h2-10,19-22,24,27-30H,11H2,1H3,(H,26,31)/t19-,20+,21+,22-,24-/m1/s1
InChI Key	SISGBWZDEMMSLV-KQWJERSKSA-N
SMILES	COC1=CC=CC=C1NC(=O)C2=C(C=C3C=CC(=CC3=C2)Br)OC4C(C(C(C(O4)CO)O)O)O
Synonyms	naphthol AS-BI beta-galactopyranoside
Canonical SMILES	COC1=CC=CC=C1NC(=O)C2=C(C=C3C=CC(=CC3=C2)Br)OC4C(C(C(C(O4)CO)O)O)O
Isomeric SMILES	COC1=CC=CC=C1NC(=O)C2=C(C=C3C=CC(=CC3=C2)Br)O[C@H]4[C@@H]([C@H]([C@H]([C@H](O4)CO)O)O)O