Cas no 937667-47-5 ((3-methylthiophen-2-yl)methyl(propan-2-yl)amine)

(3-Methylthiophen-2-yl)methyl(propan-2-yl)amine is a heterocyclic amine derivative featuring a thiophene core with a methyl substituent at the 3-position and an isopropylamino methyl group at the 2-position. This compound is of interest in organic synthesis and pharmaceutical research due to its potential as a versatile intermediate. The thiophene moiety imparts electron-rich characteristics, while the isopropylamine group enhances steric and electronic modulation, making it suitable for applications in ligand design and medicinal chemistry. Its well-defined structure allows for precise functionalization, enabling the development of targeted molecules. The compound is typically handled under inert conditions to ensure stability and purity.
(3-methylthiophen-2-yl)methyl(propan-2-yl)amine structure
937667-47-5 structure
Product Name:(3-methylthiophen-2-yl)methyl(propan-2-yl)amine
CAS No:937667-47-5
MF:C9H15NS
MW:169.28710103035
MDL:MFCD09694047
CID:2158220
Update Time:2025-11-02

(3-methylthiophen-2-yl)methyl(propan-2-yl)amine Chemical and Physical Properties

Names and Identifiers

    • Isopropyl-(3-methyl-thiophen-2-ylmethyl)-amine
    • [(3-methylthiophen-2-yl)methyl](propan-2-yl)amine
    • N-((3-Methylthiophen-2-yl)methyl)propan-2-amine
    • NE54782
    • AM101661
    • Isopropyl (3-methylthiophen-2-ylmethyl)amine
    • (3-methylthiophen-2-yl)methyl(propan-2-yl)amine
    • MDL: MFCD09694047
    • Inchi: 1S/C9H15NS/c1-7(2)10-6-9-8(3)4-5-11-9/h4-5,7,10H,6H2,1-3H3
    • InChI Key: SPXWKQPRAOWJIC-UHFFFAOYSA-N
    • SMILES: S1C=CC(C)=C1CNC(C)C

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 3
  • Complexity: 114
  • Topological Polar Surface Area: 40.3

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Additional information on (3-methylthiophen-2-yl)methyl(propan-2-yl)amine

Comprehensive Overview of (3-methylthiophen-2-yl)methyl(propan-2-yl)amine (CAS No. 937667-47-5)

The compound (3-methylthiophen-2-yl)methyl(propan-2-yl)amine (CAS No. 937667-47-5) is a specialized organic molecule that has garnered attention in various research and industrial applications. This article delves into its chemical properties, synthesis, applications, and relevance in contemporary scientific discussions.

(3-methylthiophen-2-yl)methyl(propan-2-yl)amine belongs to the class of thiophene derivatives, which are known for their versatility in pharmaceuticals, agrochemicals, and material science. The presence of a methylthiophene moiety combined with an isopropylamine group makes this compound particularly interesting for researchers exploring novel bioactive molecules.

One of the key features of CAS No. 937667-47-5 is its potential role in drug discovery. Thiophene-based compounds are frequently investigated for their pharmacological properties, including anti-inflammatory, antimicrobial, and anticancer activities. The 3-methylthiophen-2-yl scaffold in this compound could serve as a building block for designing new therapeutic agents.

In addition to pharmaceutical applications, (3-methylthiophen-2-yl)methyl(propan-2-yl)amine is also relevant in the field of organic electronics. Thiophene derivatives are widely used in the development of conductive polymers and organic semiconductors. Researchers are exploring how modifications to the methylthiophene structure can enhance the performance of these materials in devices like solar cells and LEDs.

The synthesis of CAS No. 937667-47-5 typically involves multi-step organic reactions, including alkylation and amination processes. Recent advancements in green chemistry have prompted scientists to develop more sustainable methods for producing such compounds, minimizing waste and reducing the use of hazardous reagents.

From a commercial perspective, the demand for thiophene derivatives like (3-methylthiophen-2-yl)methyl(propan-2-yl)amine is on the rise. The compound is often sourced by pharmaceutical and material science companies for research and development purposes. Its unique structure makes it a valuable intermediate in the synthesis of more complex molecules.

Environmental and safety considerations are also critical when working with CAS No. 937667-47-5. While the compound itself is not classified as hazardous, proper handling and storage are essential to ensure workplace safety. Researchers are encouraged to follow standard laboratory protocols when using this chemical.

Looking ahead, the future of (3-methylthiophen-2-yl)methyl(propan-2-yl)amine appears promising. With ongoing research into its potential applications, this compound could play a significant role in advancing fields like medicinal chemistry and renewable energy. Its adaptability and unique properties make it a subject of continued interest in the scientific community.

In summary, CAS No. 937667-47-5 represents a fascinating example of how thiophene chemistry can be leveraged for innovative solutions across multiple industries. Whether in drug development or material science, this compound exemplifies the intersection of fundamental research and practical application.

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