4-chloroaniline

Synonyms: "p-chloroaniline", "4-chlorobenzenamine", "p-chloraniline", "p-chlorophenylamine", "4-chlorophenylamine", "para-chloroaniline", "1-amino-4-chlorobenzene", "p-aminochlorobenzene", "4-aminochlorobenzene", "4-chloro-1-aminobenzene", "4-amino-1-chlorobenzene", "4-chloranilin", "4-chlorobenzeneamine", "4-chloro-phenylamine", "4-chlorobenzamine", "4-chloro aniline".

Source: 4-Chloroaniline is used as an intermediate in the production of a number of products, including agricultural chemicals, azo dyes and pigments, cosmetics, and pharmaceutical products.

Identifiers:

IUPAC Name: 4-chloroaniline
CAS Number: 106-47-8
PubChem ID: 7812
InChiKey: QSNSCYSYFYORTR-UHFFFAOYSA-N
Canonical SMILES: C1=CC(=CC=C1N)Cl

Structural Properties:

Molecular Formula: C₆H₆ClN
Molecular Weight: 127.571

Pharmacophore Features:

Number of bond donors: 1
Number of bond acceptors: 1
Number of atoms different from hydrogen: 8

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Evidence Supporting This Chemical as an Endocrine Disruptor
TEDX List of Potential Endocrine Disruptors

Bresch, H., Beck, H., Ehlermann, D., Schlaszus, H. and Urbanek, M., 1990. A long-term toxicity test comprising reproduction and growth of zebrafish with 4-chloroaniiine. Archives of environmental contamination and toxicology, 19(3), pp.419-427. DOI: https://doi.org/10.1007/BF01054987. URL: https://link.springer.com/article/10.1007/BF01054987#enumeration.
Chhabra, R.S., Huff, J.E., Haseman, J.K., Elwell, M.R. and Peters, A.C., 1991. Carcinogenicity of p-chloroaniline in rats and mice. Food and chemical toxicology, 29(2), pp.119-124. DOI: https://doi.org/10.1016/0278-6915(91)90166-5. URL: https://www.sciencedirect.com/science/article/pii/0278691591901665.