CAS 94305-64-3

2-[(6-methoxynaphthalen-2-yl)methyl]benzoic acid

Description:

2-[(6-Methoxynaphthalen-2-yl)methyl]benzoic acid, with the CAS number 94305-64-3, is an organic compound characterized by its complex structure, which includes a benzoic acid moiety and a methoxynaphthalene group. This compound typically exhibits properties associated with aromatic compounds, such as stability and relatively high melting and boiling points. The presence of the methoxy group enhances its solubility in organic solvents while potentially influencing its reactivity and interaction with biological systems. As a benzoic acid derivative, it may exhibit acidic properties, allowing it to participate in various chemical reactions, including esterification and amidation. Additionally, the naphthalene component may contribute to its photophysical properties, making it of interest in fields such as materials science and medicinal chemistry. Overall, this compound's unique structure suggests potential applications in pharmaceuticals or as a building block in organic synthesis, although specific biological activities or industrial uses would require further investigation.

Formula: C₁₉H₁₆O₃

InChI: InChI=1/C19H16O3/c1-22-17-9-8-14-10-13(6-7-15(14)12-17)11-16-4-2-3-5-18(16)19(20)21/h2-10,12H,11H2,1H3,(H,20,21)

SMILES: COc1ccc2cc(ccc2c1)Cc1ccccc1C(=O)O

a-(6-Methoxy-2-naphthyl)-o-toluic Acid (>85%)

Controlled Product

CAS: 94305-64-3

Applications α-(6-Methoxy-2-naphthyl)-o-toluic Acid is an intermediate in the synthesis of Benz[a]anthracen-3-ol (B120585), a derivative of the most potent carcinogenic hydrocarbon, 7,12-Dimethylbenz[a]anthracene (D464500).
References Harvey, R.G., et al.: J. Med. Chem., 31, 154 (1988); Lee, H.M., et al.: J. Org. Chem., 51, 3502 (1986); Smith, D.C.C., et al.: J. Chem. Soc., 673 (1962);

Formula: C₁₉H₁₆O₃

Purity: >85%

Color and Shape: Neat

Molecular weight: 292.33

Ref: TR-M260990