Cas no 107624-14-6 ((2-Phenoxyphenyl)methanamine)

(2-Phenoxyphenyl)methanamine is a secondary amine derivative featuring a phenoxy-substituted phenyl group. This compound is of interest in organic synthesis and pharmaceutical research due to its bifunctional structure, which combines an aromatic ether linkage with a reactive primary amine group. The presence of the phenoxy moiety enhances its potential as a building block for designing ligands or intermediates in medicinal chemistry. Its stability under standard conditions and compatibility with various coupling reactions make it a versatile reagent. The compound is typically characterized by NMR and HPLC for purity verification, ensuring suitability for applications requiring precise structural control.
(2-Phenoxyphenyl)methanamine structure
(2-Phenoxyphenyl)methanamine structure
Product Name:(2-Phenoxyphenyl)methanamine
CAS No:107624-14-6
MF:C13H13NO
MW:199.248423337936
CID:858463
PubChem ID:17749841
Update Time:2025-10-30

(2-Phenoxyphenyl)methanamine Chemical and Physical Properties

Names and Identifiers

    • (2-Phenoxyphenyl)methanamine
    • (2-phenoxybenzyl)amine
    • (2-phenoxyphenyl)methylamine
    • 2-phenoxy-benzylamine
    • AC1Q53SZ
    • ACMC-20mb32
    • AGN-PC-01LQQ4
    • Benzenemethanamine, 2-phenoxy-
    • CTK0D6515
    • SureCN1196716
    • 1-(2-phenoxyphenyl)methanamine
    • C77749
    • DTXSID20590019
    • AKOS000261451
    • 107624-14-6
    • SCHEMBL1196716
    • CHEMBL5195142
    • SLY
    • CS-0416095
    • CCG-356690
    • STL414992
    • EN300-59205
    • Inchi: 1S/C13H13NO/c14-10-11-6-4-5-9-13(11)15-12-7-2-1-3-8-12/h1-9H,10,14H2
    • InChI Key: WXCFCNCGPYJALB-UHFFFAOYSA-N
    • SMILES: O(C1C=CC=CC=1)C1C=CC=CC=1CN

Computed Properties

  • Exact Mass: 199.099714038g/mol
  • Monoisotopic Mass: 199.099714038g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 3
  • Complexity: 177
  • 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: 2.3
  • Topological Polar Surface Area: 35.2?2

Experimental Properties

  • PSA: 35.25000
  • LogP: 3.63790

(2-Phenoxyphenyl)methanamine Pricemore >>

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Additional information on (2-Phenoxyphenyl)methanamine

Introduction to (2-Phenoxyphenyl)methanamine and Its Significance in Modern Chemical Research

Chemical compounds play a pivotal role in the advancement of pharmaceuticals, agrochemicals, and materials science. Among these, (2-Phenoxyphenyl)methanamine (CAS No. 107624-14-6) stands out as a compound of considerable interest due to its unique structural properties and potential applications. This compound, characterized by its phenoxymethylamino functional group, has garnered attention in recent years for its role in various synthetic pathways and as a building block for more complex molecules.

The molecular structure of (2-Phenoxyphenyl)methanamine consists of a phenyl ring substituted with a phenoxy group at the 2-position, linked to an amine group through a methylene bridge. This arrangement imparts distinct electronic and steric properties to the molecule, making it a versatile intermediate in organic synthesis. The presence of both electron-donating (phenoxy) and electron-withdrawing (amine) groups allows for diverse chemical modifications, enabling the development of novel compounds with tailored functionalities.

In the realm of pharmaceutical research, (2-Phenoxyphenyl)methanamine has been explored as a precursor in the synthesis of bioactive molecules. Its structural motif is reminiscent of several pharmacophores found in therapeutic agents, suggesting potential applications in drug discovery. Recent studies have highlighted its utility in the preparation of kinase inhibitors, which are critical in treating cancers and inflammatory diseases. The amine group provides a nucleophilic site for further functionalization, while the phenoxymethyl moiety can be incorporated into larger scaffolds to enhance binding affinity and selectivity.

One notable application of (2-Phenoxyphenyl)methanamine is in the synthesis of ligands for metal-organic frameworks (MOFs). MOFs are porous materials with applications ranging from gas storage to catalysis. The compound's ability to act as a chelating agent allows it to form stable complexes with transition metals, facilitating the construction of highly ordered MOF structures. These materials are particularly valuable in carbon capture technologies and hydrogen storage systems, contributing to sustainable energy solutions.

The agrochemical industry has also shown interest in (2-Phenoxyphenyl)methanamine due to its potential as a precursor for herbicides and pesticides. Its structural features make it suitable for designing molecules that interact selectively with biological targets in plants, offering a pathway to develop more effective and environmentally friendly crop protection agents. Research is ongoing to optimize its derivatives for improved efficacy while minimizing ecological impact.

Advances in computational chemistry have further enhanced the understanding of (2-Phenoxyphenyl)methanamine's reactivity and applications. Molecular modeling studies predict its behavior in various reaction conditions, aiding chemists in designing efficient synthetic routes. These computational tools are indispensable in modern drug discovery pipelines, allowing for rapid screening of potential candidates before experimental validation.

The synthesis of (2-Phenoxyphenyl)methanamine itself presents an interesting challenge due to its delicate functional groups. Traditional methods often involve multi-step processes that require careful control of reaction conditions to avoid side products. However, recent innovations in catalytic systems have enabled more streamlined syntheses, reducing the number of steps and improving yields. Such advancements are crucial for scaling up production and making this compound more accessible for industrial applications.

Future research directions for (2-Phenoxyphenyl)methanamine include exploring its role in material science applications beyond MOFs. For instance, its incorporation into polymers could lead to novel materials with enhanced mechanical or electronic properties. Additionally, investigating its behavior under different environmental conditions may uncover new functionalities that could be exploited in green chemistry initiatives.

In conclusion, (2-Phenoxyphenyl)methanamine (CAS No. 107624-14-6) is a compound with multifaceted potential across various scientific disciplines. Its unique structure and reactivity make it a valuable intermediate in pharmaceuticals, agrochemicals, and materials science. As research continues to uncover new applications and synthetic strategies, this compound is poised to play an increasingly significant role in advancing chemical innovation.

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