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Atomfair 3-Chloro-2,6-diethylaniline C10H14ClN

Description 3-Chloro-2,6-diethylaniline (CAS No. 67330-62-5) is a high-purity organic compound with the molecular formula C10H14ClN . This aromatic amine features a chloro substituent at the 3-position and ethyl groups at the 2- and 6-positions, offering unique steric and electronic properties for advanced synthetic applications. Ideal for researchers in medicinal chemistry, agrochemical development, and material science, this compound serves as a versatile intermediate in the synthesis of complex molecules. Our product is rigorously tested to ensure ??98% purity (HPLC/GC) and is supplied in sealed, light-resistant packaging to maintain stability. Suitable for use in cross-coupling reactions, ligand synthesis, and as a precursor…

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Description

Description

3-Chloro-2,6-diethylaniline (CAS No. 67330-62-5) is a high-purity organic compound with the molecular formula C10H14ClN. This aromatic amine features a chloro substituent at the 3-position and ethyl groups at the 2- and 6-positions, offering unique steric and electronic properties for advanced synthetic applications. Ideal for researchers in medicinal chemistry, agrochemical development, and material science, this compound serves as a versatile intermediate in the synthesis of complex molecules. Our product is rigorously tested to ensure ??98% purity (HPLC/GC) and is supplied in sealed, light-resistant packaging to maintain stability. Suitable for use in cross-coupling reactions, ligand synthesis, and as a precursor for heterocyclic frameworks.

  • CAS No: 67330-62-5
  • Molecular Formula: C10H14ClN
  • Molecular Weight: 183.68
  • Exact Mass: 183.0814771
  • Monoisotopic Mass: 183.0814771
  • IUPAC Name: 3-chloro-2,6-diethylaniline
  • SMILES: CCC1=C(C(=C(C=C1)Cl)CC)N
  • Synonyms: 3-Chloro-2,6-diethylaniline, 67330-62-5, DTXSID90344561, DTXCID00295636, 625-932-0

Application

3-Chloro-2,6-diethylaniline is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its sterically hindered aniline structure makes it valuable for constructing N-heterocycles and ligands in catalysis. Researchers also employ it in the development of dyes, pigments, and advanced polymeric materials. The compound’s reactivity enables selective functionalization for targeted molecular design.

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