Cas no 42365-58-2 ((2,6-Dichlorophenyl)methanamine hydrochloride)

(2,6-Dichlorophenyl)methanamine hydrochloride is a chlorinated aromatic amine derivative, commonly utilized as a key intermediate in organic synthesis and pharmaceutical research. Its rigid aromatic structure and electron-withdrawing chlorine substituents enhance its reactivity in nucleophilic substitution and coupling reactions. The hydrochloride salt form improves stability and solubility, facilitating handling and storage. This compound is particularly valuable in the development of bioactive molecules, including potential agrochemicals and pharmacologically active agents. Its high purity and well-defined chemical properties make it a reliable building block for researchers seeking to explore structure-activity relationships or synthesize complex heterocyclic systems. The compound's consistent performance under controlled conditions ensures reproducibility in experimental applications.
(2,6-Dichlorophenyl)methanamine hydrochloride structure
42365-58-2 structure
Product Name:(2,6-Dichlorophenyl)methanamine hydrochloride
CAS No:42365-58-2
MF:C7H8Cl3N
MW:212.504118919373
MDL:MFCD09761076
CID:1028429
PubChem ID:16644432
Update Time:2025-06-07

(2,6-Dichlorophenyl)methanamine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • (2,6-Dichlorophenyl)methanamine hydrochloride
    • (2,6-Dichlorophenyl)methamine hydrochloride
    • (2,6-Dichlorophenyl)methanaminehydrochloride
    • DTXSID90586469
    • 1-(2,6-Dichlorophenyl)methanamine--hydrogen chloride (1/1)
    • CHEMBL273214
    • (2,6-dichlorophenyl)methanamine HCl
    • CS-0268963
    • 2,6-dichlorobenzylamine hydrochloride
    • XMDHRAODYVBIQW-UHFFFAOYSA-N
    • SB79006
    • EN300-300380
    • 42365-58-2
    • SCHEMBL7895201
    • AKOS002331475
    • MDL: MFCD09761076
    • Inchi: 1S/C7H7Cl2N.ClH/c8-6-2-1-3-7(9)5(6)4-10;/h1-3H,4,10H2;1H
    • InChI Key: XMDHRAODYVBIQW-UHFFFAOYSA-N
    • SMILES: ClC1C=CC=C(C=1CN)Cl.Cl

Computed Properties

  • Exact Mass: 210.972232g/mol
  • Monoisotopic Mass: 210.972232g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 97.8
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 26?2

(2,6-Dichlorophenyl)methanamine hydrochloride Pricemore >>

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Additional information on (2,6-Dichlorophenyl)methanamine hydrochloride

(2,6-Dichlorophenyl)methanamine Hydrochloride: A Comprehensive Overview

The compound with CAS No. 42365-58-2, commonly referred to as (2,6-Dichlorophenyl)methanamine hydrochloride, is a significant entity in the fields of organic chemistry and pharmacology. This compound has garnered attention due to its unique structural properties and potential applications in various industries. In this article, we delve into the chemical structure, synthesis methods, physical properties, and biological activities of this compound, while incorporating the latest research findings to provide a comprehensive understanding.

Chemical Structure and Synthesis

(2,6-Dichlorophenyl)methanamine hydrochloride consists of a benzene ring substituted with two chlorine atoms at the 2 and 6 positions, attached to a methanamine group (CH?NH?) and a hydrochloride ion (Cl?). The molecule's structure is characterized by the presence of electron-withdrawing chlorine atoms, which influence its reactivity and stability. Recent studies have explored novel synthetic routes for this compound, including microwave-assisted synthesis and catalytic methods that enhance reaction efficiency and reduce environmental impact.

Physical Properties

The physical properties of (2,6-Dichlorophenyl)methanamine hydrochloride are critical for its application in various fields. It exhibits a melting point of approximately 180°C and is sparingly soluble in water but dissolves readily in organic solvents such as dichloromethane and ethyl acetate. These properties make it suitable for use in pharmaceutical formulations and chemical intermediates.

Biological Activity and Applications

Recent research has highlighted the potential of (2,6-Dichlorophenyl)methanamine hydrochloride as a bioactive compound with applications in drug discovery. Studies have demonstrated its ability to inhibit certain enzymes associated with neurodegenerative diseases, making it a promising candidate for further investigation in the development of therapeutic agents. Additionally, its role as an intermediate in the synthesis of more complex molecules has been explored in recent patents.

Safety and Toxicological Profile

Understanding the safety profile of (2,6-Dichlorophenyl)methanamine hydrochloride is essential for its safe handling and application. Preliminary toxicological studies indicate that it exhibits low acute toxicity when administered orally or dermally. However, further long-term studies are required to fully assess its safety profile and environmental impact.

In conclusion, (2,6-Dichlorophenyl)methanamine hydrochloride is a versatile compound with a wide range of potential applications. Its unique chemical structure, coupled with recent advancements in synthesis and biological activity studies, positions it as an important entity in contemporary chemical research.

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