N-Ethyl-1-naphthalenamine, with the CAS number 118-44-5, is an organic compound characterized by its structure, which consists of a naphthalene ring substituted with an ethyl group and an amino group. This compound appears as a pale yellow to brown liquid or solid, depending on its purity and temperature. It is known for its aromatic properties and is often used as an intermediate in the synthesis of dyes, pigments, and other organic compounds. N-Ethyl-1-naphthalenamine exhibits moderate solubility in organic solvents, while its solubility in water is limited. The compound can undergo various chemical reactions, including electrophilic substitution due to the presence of the amino group, which can act as a nucleophile. Safety considerations are important, as it may pose health risks upon exposure, necessitating appropriate handling and storage measures. Overall, N-Ethyl-1-naphthalenamine is a valuable compound in organic synthesis, with applications in the chemical industry.

N-Ethyl-1-naphthalenamine

118-44-5: 1-(Ethylamino)naphthalene, 1-Naphthalenamine, N-ethyl-, 1-Naphthylamine, N-ethyl-, Ethyl-α-naphthylamine, N-Ethyl-1-aminonaphthalene, N-Ethyl-1-naphthalenamine, N-Ethyl-1-naphthylamine, N-Ethyl-α-naphthylamine, N-ethylnaphthalen-1-amine, NSC 8636

N-Ethylnaphthalen-1-amine

N-Ethyl-1-naphthylamine

N-Ethyl-1-naphthylamine is an alkylating agent that can react with DNA, RNA and proteins. It reacts with a carbonyl group to form an alkylthio group and an amine, which can then react with other molecules to form covalent bonds. N-Ethyl-1-naphthylamine is carcinogenic and genotoxic, meaning it causes cancer and damages the genetic information of cells. The carcinogenic activity of this compound has been linked to its ability to methylate DNA and form covalent bonds with amino groups on proteins.

CAS 118-44-5: N-Ethyl-1-naphthalenamine

N-Ethylnaphthalen-1-amine

Ref: 54-OR480574

N-Ethyl-1-naphthylamine

Ref: 7W-GT1548

N-Ethyl-1-naphthylamine

Ref: 3D-FE38728