Cas no 2228572-71-0 (2,2-dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine)

2,2-Dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine is a specialized organic compound featuring a thiophene core substituted with a propyl group and an amine-functionalized side chain. The 2,2-dimethyl substitution on the propan-1-amine moiety enhances steric hindrance, potentially improving stability and selectivity in synthetic applications. The thiophene ring contributes to electronic delocalization, making this compound useful in materials science or pharmaceutical intermediates. Its structural design allows for further functionalization, offering versatility in organic synthesis. The amine group provides a reactive site for derivatization, while the propyl chain may influence solubility and lipophilicity. This compound is of interest for research in medicinal chemistry and functional materials due to its balanced steric and electronic properties.
2,2-dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine structure
2228572-71-0 structure
Product Name:2,2-dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine
CAS No:2228572-71-0
MF:C12H21NS
MW:211.366842031479
CID:5838143
PubChem ID:165966030
Update Time:2025-06-13

2,2-dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine Chemical and Physical Properties

Names and Identifiers

    • 2,2-dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine
    • 2228572-71-0
    • EN300-1997653
    • Inchi: 1S/C12H21NS/c1-4-5-10-6-7-11(14-10)8-12(2,3)9-13/h6-7H,4-5,8-9,13H2,1-3H3
    • InChI Key: BOUTYMQVQLHLAV-UHFFFAOYSA-N
    • SMILES: S1C(=CC=C1CC(C)(C)CN)CCC

Computed Properties

  • Exact Mass: 211.13947085g/mol
  • Monoisotopic Mass: 211.13947085g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 5
  • Complexity: 168
  • 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: 3.3
  • Topological Polar Surface Area: 54.3?2

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2,2-dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine Related Literature

Additional information on 2,2-dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine

Research Brief on 2,2-dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine (CAS: 2228572-71-0): Recent Advances and Applications

The compound 2,2-dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine (CAS: 2228572-71-0) has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This molecule, characterized by its unique thiophene-based structure, has shown promising potential in various therapeutic applications. Recent studies have focused on its synthesis, pharmacological properties, and mechanisms of action, positioning it as a candidate for further drug development.

One of the key areas of interest is the compound's interaction with central nervous system (CNS) targets. Preliminary research indicates that 2,2-dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine exhibits affinity for specific neurotransmitter receptors, suggesting potential applications in neurological disorders. The compound's structural features, including the propylthiophene moiety, contribute to its bioavailability and metabolic stability, making it a viable candidate for further optimization.

Recent synthetic approaches have improved the yield and purity of 2,2-dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine, facilitating more robust pharmacological evaluations. Advanced techniques such as high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy have been employed to characterize the compound, ensuring its consistency and quality for research purposes. These advancements have enabled researchers to explore its therapeutic potential with greater precision.

In vitro and in vivo studies have provided insights into the compound's pharmacokinetic and pharmacodynamic profiles. For instance, animal models have demonstrated its ability to cross the blood-brain barrier, a critical factor for CNS-targeted therapies. Additionally, its metabolic pathways have been elucidated, revealing minimal toxicity and favorable excretion profiles. These findings underscore the compound's potential as a lead molecule for further development.

Looking ahead, ongoing research aims to explore the broader applications of 2,2-dimethyl-3-(5-propylthiophen-2-yl)propan-1-amine, including its potential use in combination therapies and as a scaffold for derivative compounds. Collaborative efforts between academic institutions and pharmaceutical companies are expected to accelerate its translation into clinical trials. As the body of evidence grows, this compound may emerge as a cornerstone in the development of novel therapeutics for complex diseases.

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