Cas no 34843-88-4 ((2,5-Dimethylthiophen-3-yl)methanamine)

(2,5-Dimethylthiophen-3-yl)methanamine structure
34843-88-4 structure
Product Name:(2,5-Dimethylthiophen-3-yl)methanamine
CAS No:34843-88-4
MF:C7H11NS
MW:141.23394036293
MDL:MFCD08060576
CID:2618714
PubChem ID:46784114
Update Time:2025-11-02

(2,5-Dimethylthiophen-3-yl)methanamine Chemical and Physical Properties

Names and Identifiers

    • (2,5-dimethylthiophen-3-yl)methanamine
    • [(2,5-Dimethyl-3-thienyl)methyl]amine hydrochloride
    • C-(2,5-Dimethyl-thiophen-3-yl)-methylamine
    • NE57186
    • (2,5-dimethyl-3-thienyl)methanamine, AldrichCPR
    • 1-(2,5-dimethyl-3-thienyl)methanamine hydrochloride
    • Z1258578176
    • (2,5-Dimethylthiophen-3-yl)methanamine
    • MDL: MFCD08060576
    • Inchi: 1S/C7H11NS/c1-5-3-7(4-8)6(2)9-5/h3H,4,8H2,1-2H3
    • InChI Key: DXMACNBVEGINGQ-UHFFFAOYSA-N
    • SMILES: S1C(C)=CC(CN)=C1C

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 1
  • Complexity: 94.9
  • Topological Polar Surface Area: 54.3

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Additional information on (2,5-Dimethylthiophen-3-yl)methanamine

Comprehensive Overview of (2,5-Dimethylthiophen-3-yl)methanamine (CAS No. 34843-88-4): Properties, Applications, and Industry Insights

(2,5-Dimethylthiophen-3-yl)methanamine (CAS No. 34843-88-4) is a specialized organic compound belonging to the thiophene derivatives family. Its molecular structure, featuring a methanamine group attached to a 2,5-dimethylthiophene ring, makes it a valuable intermediate in pharmaceutical and material science research. The compound's unique heterocyclic framework contributes to its versatility in synthetic applications, particularly in the development of bioactive molecules and functional materials.

Recent advancements in drug discovery have highlighted the importance of thiophene-based compounds like (2,5-Dimethylthiophen-3-yl)methanamine. Researchers are increasingly exploring its potential as a building block for central nervous system (CNS) therapeutics, owing to its ability to cross the blood-brain barrier. The compound's structural modularity allows for precise modifications, addressing trending topics such as personalized medicine and targeted drug delivery systems.

In the field of organic electronics, 34843-88-4 has gained attention for its potential in designing conductive polymers and semiconductor materials. With the global push toward green energy solutions, this compound's electron-rich thiophene core makes it a candidate for organic photovoltaics (OPVs) and OLED technologies. Industry reports suggest growing demand for such specialized intermediates in next-generation display applications.

The synthesis of (2,5-Dimethylthiophen-3-yl)methanamine typically involves multistep organic transformations, with recent studies focusing on catalytic methods to improve yield and sustainability. Modern flow chemistry techniques have shown particular promise in scaling up production while minimizing environmental impact—a crucial consideration given current ESG (Environmental, Social, and Governance) investment trends in the chemical sector.

Analytical characterization of CAS 34843-88-4 employs advanced techniques including NMR spectroscopy, mass spectrometry, and HPLC analysis. These methods ensure the high purity required for research applications, addressing common quality concerns in fine chemical synthesis. The compound typically appears as a colorless to pale yellow liquid with specific storage requirements to maintain stability.

Market analysis indicates growing interest in thiophene derivatives across multiple industries. Frequently searched questions about (2,5-Dimethylthiophen-3-yl)methanamine include its solubility profile, commercial availability, and handling precautions. While not classified as hazardous under standard regulations, proper laboratory safety protocols should always be observed when working with this compound.

Future research directions for 34843-88-4 may explore its potential in catalysis and asymmetric synthesis, particularly in constructing chiral amine structures. The compound's compatibility with microwave-assisted reactions and continuous manufacturing processes positions it well for adoption in Industry 4.0 chemical production paradigms.

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