Description

Benzenamine, N-(2-chloroethyl)-N-ethyl-3-methyl- (CAS No. 22564-43-8) is a high-purity organic compound with the molecular formula C₁₁H₁₆ClN. This specialized chemical is widely used in pharmaceutical research, agrochemical synthesis, and as an intermediate in fine chemical manufacturing. Its unique structure, featuring both chloroethyl and ethyl substituents on a methylated benzene ring, makes it valuable for developing novel bioactive molecules. Our product is rigorously tested to ensure >98% purity (HPLC) and is supplied in sealed, light-resistant containers to maintain stability. Researchers can rely on its consistent quality for reproducible results in nucleophilic substitution reactions, alkylation studies, and heterocyclic compound synthesis.

Properties

• CAS Number: 22564-43-8
• Complexity: 138
• IUPAC Name: N-(2-chloroethyl)-N-ethyl-3-methyl-aniline
• InChI: InChI=1S/C11H16ClN/c1-3-13(8-7-12)11-6-4-5-10(2)9-11/h4-6,9H,3,7-8H2,1-2H3
• InChI Key: DLRPOOIAFCOLII-UHFFFAOYSA-N
• Exact Mass: 197.0971272
• Molecular Formula: C11H16ClN
• Molecular Weight: 197.70
• SMILES: CCN(CCCl)C1=CC=CC(=C1)C
• Topological: 3.2
• Monoisotopic Mass: 197.0971272
• Synonyms: 22564-43-8, N-(2-Chloroethyl)-N-ethyl-m-toluidine, Benzenamine, N-(2-chloroethyl)-N-ethyl-3-methyl-, EINECS 245-082-0, DTXSID7066809, 1-(Ethyl(2′-chloroethyl)amino)-3-methylbenzene, Benzeneamine, N-(2-chloroethyl)-N-ethyl-3-methyl-, N-(2-Chloroethyl)-N-ethyl-3-methylbenzenamine, DTXCID4036722, N-(2-chloroethyl)-N-ethyl-3-methylaniline, N-Ethyl-N-chloroethyl-3-toluidine, n-Ethyl-n-chloro ethyl-m-toluidine, N-Ethyl-N-chloroethy, N-ethyl-N-(beta-chloroethyl)-m-toluidine, VH4C8S8GGW, SCHEMBL2405546, AKOS010540584, AS-76988, NS00027215

This compound serves as a key intermediate in the synthesis of potential pharmaceutical agents, particularly those targeting neurological pathways. It’s utilized in research laboratories for developing novel quaternary ammonium compounds with potential biological activity. The chloroethyl moiety makes it valuable for alkylation reactions in medicinal chemistry. Scientists employ it in structure-activity relationship studies of CNS-active compounds.

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