CAS 5959-54-6
:2-Naphthalenecarboxylic acid, 3-amino-, ethyl ester
Description:
2-Naphthalenecarboxylic acid, 3-amino-, ethyl ester, also known as ethyl 3-amino-2-naphthoate, is an organic compound characterized by its naphthalene ring structure substituted with a carboxylic acid and an amino group. This compound typically appears as a solid or crystalline substance and is soluble in organic solvents. It possesses both acidic and basic functional groups, which can participate in various chemical reactions, making it useful in synthetic organic chemistry. The presence of the naphthalene moiety contributes to its aromatic properties, while the ethyl ester group enhances its reactivity and solubility. This compound may be utilized in the synthesis of pharmaceuticals, dyes, or agrochemicals, owing to its potential biological activity and ability to serve as an intermediate in chemical reactions. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Proper laboratory practices should be followed when working with this substance.
Formula:C13H13NO2
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Found 1 products.
Ethyl 3-aminonaphthalene-2-carboxylate
CAS:<p>Ethyl 3-aminonaphthalene-2-carboxylate is a molecule that is used in the synthesis of various organic compounds. It can be produced by reacting aniline with copper(II) chloride and dichloroethane in the presence of a base. This reaction requires irradiation, which will produce ethyl 3-aminonaphthalene-2-carboxylate from the aniline and copper(II) chloride at a rate dependent on the reaction time. The product yields are high, but it must be purified before use to remove any traces of dichloroethane or aniline. Ethyl 3-aminonaphthalene-2-carboxylate has been shown to selectively react with dipyridine to form 2,5-diphenylpyridine, which is a target molecule for this reaction.</p>Formula:C13H13NO2Purity:Min. 95%Molecular weight:215.25 g/mol
