CAS 91902-58-8
:4-ethylnaphthalene-1-carboxylic acid
Description:
4-Ethylnaphthalene-1-carboxylic acid is an organic compound characterized by its naphthalene backbone substituted with an ethyl group and a carboxylic acid functional group. This compound typically appears as a solid at room temperature and is soluble in organic solvents, reflecting its aromatic nature. The presence of the carboxylic acid group imparts acidic properties, allowing it to participate in various chemical reactions, such as esterification and amidation. Its structure suggests potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Additionally, the compound may exhibit interesting physical properties, such as melting and boiling points influenced by its molecular interactions. As with many aromatic compounds, it may also display fluorescence under certain conditions. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper precautions are taken. Overall, 4-ethylnaphthalene-1-carboxylic acid is a versatile compound with potential utility in various chemical applications.
Formula:C13H12O2
InChI:InChI=1/C13H12O2/c1-2-9-7-8-12(13(14)15)11-6-4-3-5-10(9)11/h3-8H,2H2,1H3,(H,14,15)
SMILES:CCc1ccc(c2ccccc12)C(=O)O
Synonyms:- 4-Ethyl-1-naphthoic acid
- 4-ethyl-1-Naphthalenecarboxylicacid
- 4-Ethyl-1-naphthalenecarboxylic acid
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Found 4 products.
1-Naphthalenecarboxylicacid, 4-ethyl-
CAS:Formula:C13H12O2Purity:95%Color and Shape:SolidMolecular weight:200.23324-Ethyl-1-naphthoic Acid
CAS:Controlled ProductApplications Used in the preparation of antimalarial compounds. It also shows some plant-growth activity.
References Bachmann, W. et al.: J. Am. Chem. Soc. 72, 4911 (1950); Fujita, T. et al.: Agr. Biol. Chem. 25, 719 (1961)Formula:C13H12O2Color and Shape:NeatMolecular weight:200.23
