Cas no 104293-83-6 ((2-Propylphenyl)methanamine)

(2-Propylphenyl)methanamine is a substituted benzylamine derivative featuring a propyl group at the ortho position of the phenyl ring. This structural configuration imparts distinct chemical properties, making it a valuable intermediate in organic synthesis and pharmaceutical applications. The compound’s amine functionality allows for further derivatization, enabling the formation of amides, imines, or other nitrogen-containing compounds. Its aromatic ring contributes to stability, while the propyl substituent may influence solubility and reactivity. (2-Propylphenyl)methanamine is particularly useful in the development of fine chemicals, agrochemicals, and bioactive molecules, where precise functional group manipulation is required. Proper handling and storage under inert conditions are recommended to maintain its integrity.
(2-Propylphenyl)methanamine structure
(2-Propylphenyl)methanamine structure
Product Name:(2-Propylphenyl)methanamine
CAS No:104293-83-6
MF:C10H15N
MW:149.232802629471
CID:1089051
PubChem ID:21923728
Update Time:2025-05-21

(2-Propylphenyl)methanamine Chemical and Physical Properties

Names and Identifiers

    • (2-Propylphenyl)methanamine
    • EN300-751108
    • 104293-83-6
    • 1-(2-Propylphenyl)methanamine
    • SCHEMBL283610
    • AKOS006361737
    • DTXSID80620169
    • Inchi: 1S/C10H15N/c1-2-5-9-6-3-4-7-10(9)8-11/h3-4,6-7H,2,5,8,11H2,1H3
    • InChI Key: PMVKAPTVFIPZNA-UHFFFAOYSA-N
    • SMILES: NCC1C=CC=CC=1CCC

Computed Properties

  • Exact Mass: 149.120449483g/mol
  • Monoisotopic Mass: 149.120449483g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 3
  • Complexity: 101
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.1
  • Topological Polar Surface Area: 26?2

(2-Propylphenyl)methanamine Pricemore >>

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Additional information on (2-Propylphenyl)methanamine

(2-Propylphenyl)methanamine: A Comprehensive Overview

The compound with CAS No. 104293-83-6, commonly referred to as (2-Propylphenyl)methanamine, is a fascinating molecule with a unique structure and diverse applications. This compound belongs to the class of aromatic amines, which are widely used in various industries due to their versatile chemical properties. The molecular formula of (2-Propylphenyl)methanamine is C13H19N, and it consists of a phenyl ring substituted with a propyl group at the 2-position and an amine group attached to the methyl group.

Recent studies have highlighted the potential of (2-Propylphenyl)methanamine in the field of drug discovery. Researchers have explored its role as a building block in the synthesis of bioactive compounds, particularly in the development of new pharmaceutical agents. The compound's ability to form stable bonds with other molecules makes it an ideal candidate for creating complex molecular architectures. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated that derivatives of (2-Propylphenyl)methanamine exhibit promising anti-inflammatory properties, suggesting its potential use in treating chronic inflammatory diseases.

In addition to its pharmaceutical applications, (2-Propylphenyl)methanamine has found significant use in the field of materials science. Its unique electronic properties make it a valuable component in the synthesis of advanced materials such as conductive polymers and organic semiconductors. A recent breakthrough in this area involves the incorporation of (2-Propylphenyl)methanamine into polymer blends to enhance their thermal stability and mechanical strength. This innovation has opened new avenues for its application in high-performance materials used in aerospace and automotive industries.

The synthesis of (2-Propylphenyl)methanamine typically involves a multi-step process that includes nucleophilic substitution and reduction reactions. Researchers have been focusing on optimizing these processes to improve yield and reduce production costs. A 2023 paper in Green Chemistry reported a novel catalytic method for synthesizing (2-Propylphenyl)methanamine using renewable feedstocks, which significantly reduces the environmental impact of its production.

From an environmental perspective, understanding the fate and transport of (2-Propylphenyl)methanamine in natural systems is crucial for assessing its potential ecological risks. Recent studies have investigated its biodegradation pathways under various environmental conditions. Findings indicate that while the compound is relatively stable under aerobic conditions, it undergoes rapid degradation in anaerobic environments, which is promising for minimizing its persistence in ecosystems.

In conclusion, (2-Propylphenyl)methanamine is a versatile compound with significant potential across multiple disciplines. Its role as a building block in drug discovery, its application in materials science, and its environmentally friendly synthesis methods highlight its importance in contemporary research. As ongoing studies continue to uncover new applications and optimize existing processes, this compound is poised to play an increasingly vital role in advancing technological and medical frontiers.

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