Cas no 83304-60-3 (N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine)

N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine is a synthetic organic compound featuring a benzylamine core substituted with a 2,4-dimethoxyphenyl group. This structure imparts unique electronic and steric properties, making it valuable as an intermediate in pharmaceutical and agrochemical research. The dimethoxy groups enhance solubility in polar organic solvents, facilitating further functionalization. Its amine functionality allows for versatile reactivity, including reductive amination or acylation, enabling the synthesis of more complex derivatives. The compound's stability under standard conditions ensures reliable handling and storage. Researchers may find it particularly useful in the development of bioactive molecules due to its balanced lipophilicity and potential for hydrogen bonding interactions.
N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine structure
83304-60-3 structure
Product Name:N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine
CAS No:83304-60-3
MF:C16H19NO2
MW:257.327564477921
MDL:MFCD01135686
CID:724415
PubChem ID:784822
Update Time:2025-08-05

N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine Chemical and Physical Properties

Names and Identifiers

    • N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine
    • Benzenemethanamine,2,4-dimethoxy-N-(phenylmethyl)-
    • Benzyl-(2,4-dimethoxy-benzyl)-amine
    • N-(2,4-dimethoxybenzyl)(phenyl)methanamine
    • benzyl[(2,4-dimethoxyphenyl)methyl]amine
    • MFCD01135686
    • AKOS000227353
    • SCHEMBL8880359
    • Ethyl4-Chloroquinazoline-2-carboxylate
    • N-[(2,4-dimethoxyphenyl)methyl]-1-phenylmethanamine
    • Oprea1_311295
    • AS-65872
    • SR-01000370498-1
    • 83304-60-3
    • CS-0061945
    • NUNNRGRUURRZRA-UHFFFAOYSA-N
    • W17311
    • 2,?4-?Dimethoxy-?N-?(phenylmethyl)?-benzenemethanamine
    • DTXSID10354849
    • benzyl (2,4-dimethoxybenzyl)-amine
    • SR-01000370498
    • DB-334967
    • SY062870
    • MDL: MFCD01135686
    • Inchi: 1S/C16H19NO2/c1-18-15-9-8-14(16(10-15)19-2)12-17-11-13-6-4-3-5-7-13/h3-10,17H,11-12H2,1-2H3
    • InChI Key: NUNNRGRUURRZRA-UHFFFAOYSA-N
    • SMILES: O(C)C1C=C(C=CC=1CNCC1C=CC=CC=1)OC

Computed Properties

  • Exact Mass: 258.149404
  • Monoisotopic Mass: 258.149404
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 6
  • Complexity: 241
  • 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
  • Topological Polar Surface Area: 35.1
  • XLogP3: 2.7

Experimental Properties

  • Boiling Point: 378.1°C at 760 mmHg
  • Flash Point: 158.7°C

N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine Security Information

  • Hazardous Material Identification: Xi
  • HazardClass:IRRITANT

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N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine Related Literature

Additional information on N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine

Introduction to N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine (CAS No. 83304-60-3)

N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine, a compound with the chemical formula C14H17N, is a significant molecule in the field of pharmaceutical chemistry. This compound is characterized by its unique structural features, which include a benzyl group and a dimethoxyphenyl moiety. The presence of these functional groups makes it a valuable intermediate in the synthesis of various pharmacologically active agents. The CAS number 83304-60-3 uniquely identifies this compound and distinguishes it from other chemical entities.

The benzyl group in N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine contributes to the compound's solubility and stability, making it an ideal candidate for further derivatization and functionalization. The dimethoxyphenyl moiety, on the other hand, imparts specific electronic and steric properties that can influence its interactions with biological targets. These properties have been extensively studied in recent years, leading to a deeper understanding of its potential applications in drug development.

Recent research has highlighted the importance of N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine in the synthesis of novel therapeutic agents. Its structural framework has been utilized in the development of compounds with anti-inflammatory, anticancer, and antimicrobial properties. For instance, studies have demonstrated its role as a precursor in the synthesis of kinase inhibitors, which are crucial in treating various forms of cancer. The dimethoxyphenyl group has been shown to enhance binding affinity to target proteins, thereby improving the efficacy of these inhibitors.

The pharmaceutical industry has shown significant interest in this compound due to its versatility and potential therapeutic benefits. Researchers have explored its use in developing treatments for neurological disorders, where its ability to cross the blood-brain barrier is particularly valuable. Additionally, its derivatives have been investigated for their potential as antiviral agents, offering hope for new strategies in combating infectious diseases.

In terms of synthetic methodologies, N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine serves as a key intermediate in multi-step organic reactions. Its synthesis typically involves the reaction of benzaldehyde derivatives with appropriate nitrogen-containing reagents under controlled conditions. Advances in catalytic systems have further optimized these reactions, making them more efficient and environmentally friendly. These improvements have not only enhanced the yield but also reduced the formation of unwanted byproducts.

The compound's stability under various conditions has also been a subject of interest. Studies have shown that N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine maintains its structural integrity when exposed to light and oxygen, making it suitable for long-term storage and transportation. This stability is crucial for pharmaceutical applications where product shelf life is a critical factor.

From a regulatory perspective, the handling and use of N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine are governed by strict guidelines to ensure safety and efficacy. Manufacturers must adhere to Good Manufacturing Practices (GMP) to guarantee the quality and consistency of the final products. Additionally, rigorous testing protocols are employed to assess its compatibility with other pharmaceutical ingredients and its overall safety profile.

The future prospects of N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine are promising, with ongoing research exploring new applications and improving existing synthetic routes. The integration of computational chemistry and artificial intelligence has accelerated the discovery process by predicting potential drug candidates and optimizing their properties before experimental synthesis. This interdisciplinary approach has opened new avenues for innovation in pharmaceutical chemistry.

In conclusion, N-Benzyl-1-(2,4-dimethoxyphenyl)methanamine (CAS No. 83304-60-3) is a versatile and valuable compound with significant implications in drug development. Its unique structural features and functional groups make it an ideal candidate for synthesizing novel therapeutic agents with broad applications in medicine. As research continues to uncover new possibilities, this compound is poised to play an even greater role in addressing global health challenges.

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