Cas no 1050214-15-7 (N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride)

N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride is a brominated aromatic compound featuring a cyclopropylamine moiety, commonly utilized in pharmaceutical and agrochemical research. Its structural framework, incorporating both a bromophenyl group and a cyclopropane ring, makes it a valuable intermediate in the synthesis of bioactive molecules. The hydrochloride salt form enhances stability and solubility, facilitating handling and storage. This compound is particularly relevant in medicinal chemistry for developing receptor-targeting agents due to its potential as a building block for modulators of central nervous system (CNS) activity. Its well-defined chemical properties and purity ensure reproducibility in synthetic applications.
N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride structure
1050214-15-7 structure
Product Name:N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride
CAS No:1050214-15-7
MF:C10H13BrClN
MW:262.573920965195
MDL:MFCD07111375
CID:3151229
PubChem ID:17294991
Update Time:2025-08-05

N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride Chemical and Physical Properties

Names and Identifiers

    • N-(3-bromobenzyl)cyclopropanamine hydrochloride
    • N-(3-Bromobenzyl)cyclopropanaminehydrochloride
    • N-(3-Bromobenzyl)cyclopropanamine HCl
    • AKOS027426017
    • EN300-56145
    • Z857667052
    • 1050214-15-7
    • BS-41355
    • N-[(3-bromophenyl)methyl]cyclopropanamine hydrochloride
    • CS-0251802
    • N-[(3-bromophenyl)methyl]cyclopropanamine;hydrochloride
    • MFCD07111375
    • ASB21415
    • N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride
    • MDL: MFCD07111375
    • Inchi: 1S/C10H12BrN.ClH/c11-9-3-1-2-8(6-9)7-12-10-4-5-10;/h1-3,6,10,12H,4-5,7H2;1H
    • InChI Key: FMVAAAYJFHFIFB-UHFFFAOYSA-N
    • SMILES: BrC1=CC=CC(=C1)CNC1CC1.Cl

Computed Properties

  • Exact Mass: 260.99199Da
  • Monoisotopic Mass: 260.99199Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 3
  • Complexity: 145
  • 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: 12?2

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Additional information on N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride

N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride: A Comprehensive Overview

The compound N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride (CAS No. 1050214-15-7) is a fascinating molecule with significant potential in various scientific and industrial applications. This compound, often abbreviated as methylcyclopropanamine hydrochloride, has garnered attention due to its unique chemical structure and promising properties. The 3-bromophenyl group attached to the cyclopropane ring introduces interesting electronic and steric effects, making it a valuable compound for research and development in fields such as pharmaceuticals, agrochemicals, and materials science.

Recent studies have highlighted the importance of methylcyclopropanamine hydrochloride in drug discovery. Its ability to act as a precursor for bioactive molecules has been extensively explored. For instance, researchers have utilized this compound to synthesize novel neurotransmitter analogs, which show potential in treating neurological disorders such as Alzheimer's disease and Parkinson's disease. The 3-bromophenyl group plays a crucial role in enhancing the bioavailability and selectivity of these analogs, making them promising candidates for further clinical trials.

In addition to its pharmaceutical applications, N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride has found utility in the synthesis of advanced materials. Its cyclopropane ring is known for its high strain energy, which can be harnessed to create robust polymers and high-performance composites. Recent advancements in polymer chemistry have demonstrated that incorporating this compound into polymer matrices can significantly improve mechanical properties such as tensile strength and thermal stability.

The synthesis of methylcyclopropanamine hydrochloride involves a multi-step process that combines organic synthesis techniques with modern catalytic methods. The key steps include the bromination of phenyl rings, cyclopropane ring formation, and amine functionalization. Researchers have optimized these steps to achieve higher yields and better purity levels, ensuring that the compound meets the stringent requirements of various industries.

One of the most exciting developments involving N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride is its use in green chemistry initiatives. By employing environmentally friendly solvents and catalysts, chemists have successfully reduced the environmental footprint of its production process. This shift toward sustainable practices aligns with global efforts to promote eco-friendly manufacturing methods.

Moreover, the compound's role in agrochemical research cannot be overlooked. Studies have shown that derivatives of methylcyclopropanamine hydrochloride exhibit potent insecticidal and fungicidal activities. These findings have opened new avenues for developing safer and more effective pesticides, which are essential for addressing food security challenges worldwide.

Looking ahead, the future of N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride seems bright. Ongoing research is focused on exploring its potential in nanotechnology applications, where its unique properties could contribute to the development of next-generation nanomaterials. Additionally, collaborations between academic institutions and industry leaders are expected to accelerate the commercialization of this compound across multiple sectors.

In conclusion, N-(3-Bromophenyl)methylcyclopropanamine Hydrochloride (CAS No. 1050214-15-7) is a versatile compound with a wide range of applications across various fields. Its unique chemical structure, coupled with recent advancements in synthesis and application techniques, positions it as a key player in modern scientific research. As ongoing studies continue to uncover new possibilities for this compound, it is poised to make significant contributions to both academic and industrial advancements.

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