Cas no 1504153-40-5 (2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid)

2-Methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid is a cyclobutane-derived carboxylic acid featuring a propylsulfanyl substituent at the 1-position. This compound is of interest in synthetic organic chemistry due to its strained cyclobutane ring, which can impart unique reactivity in ring-opening or functionalization reactions. The presence of the thioether group (propylsulfanyl) offers potential for further derivatization, such as oxidation to sulfoxides or sulfones, enhancing its utility as a versatile intermediate. The carboxylic acid moiety provides a handle for amidation, esterification, or other transformations, making it valuable for pharmaceutical or agrochemical applications. Its structural features may also contribute to steric and electronic effects in ligand design or catalysis.
2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid structure
1504153-40-5 structure
Product Name:2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid
CAS No:1504153-40-5
MF:C9H16O2S
MW:188.287141799927
CID:6247900
PubChem ID:66430136
Update Time:2025-11-02

2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid
    • 1504153-40-5
    • AKOS015775284
    • EN300-1122329
    • Inchi: 1S/C9H16O2S/c1-3-6-12-9(8(10)11)5-4-7(9)2/h7H,3-6H2,1-2H3,(H,10,11)
    • InChI Key: DZHIXMFLDXMPBY-UHFFFAOYSA-N
    • SMILES: S(CCC)C1(C(=O)O)CCC1C

Computed Properties

  • Exact Mass: 188.08710092g/mol
  • Monoisotopic Mass: 188.08710092g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 4
  • Complexity: 181
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 2
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.5
  • Topological Polar Surface Area: 62.6?2

2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid Pricemore >>

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Additional information on 2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid

Research Brief on 2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid (CAS: 1504153-40-5): Recent Advances and Applications

2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid (CAS: 1504153-40-5) has recently emerged as a compound of significant interest in the field of chemical biology and medicinal chemistry. This cyclobutane derivative, characterized by its unique structural features, has shown promising potential in various therapeutic applications. Recent studies have focused on its synthesis, biological activity, and potential as a scaffold for drug development. This research brief aims to summarize the latest findings and highlight the key advancements related to this compound.

The synthesis of 2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid has been optimized in recent studies, with a focus on improving yield and purity. Researchers have employed advanced catalytic methods and green chemistry principles to achieve efficient and sustainable production. The compound's structural complexity, particularly the cyclobutane ring and the propylsulfanyl moiety, has posed challenges in synthesis, but recent breakthroughs have addressed these issues, enabling larger-scale production for further studies.

In terms of biological activity, preliminary investigations have revealed that 2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid exhibits notable interactions with specific enzymatic targets. Recent in vitro studies have demonstrated its inhibitory effects on certain proteases and kinases, suggesting potential applications in oncology and inflammatory diseases. The compound's mechanism of action is currently under investigation, with early data indicating that it may act as an allosteric modulator or competitive inhibitor, depending on the target enzyme.

One of the most exciting developments is the exploration of this compound as a building block for novel drug candidates. Its rigid cyclobutane core provides a stable framework for structural modifications, while the carboxylic acid and sulfanyl groups offer sites for further functionalization. Recent medicinal chemistry efforts have focused on creating derivatives with enhanced pharmacokinetic properties and target specificity. Several patent applications have been filed in the past year, highlighting the pharmaceutical industry's growing interest in this chemical scaffold.

The compound's potential in drug delivery systems has also been investigated. Due to its amphiphilic nature, 2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid has shown promise in forming stable micelles and liposomes. Recent studies have explored its use as a component in nanoparticle formulations for targeted drug delivery, particularly in cancer therapy. The compound's ability to improve solubility and bioavailability of hydrophobic drugs makes it an attractive candidate for formulation development.

Safety and toxicity profiles of 2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid are currently being evaluated in preclinical studies. Early results suggest a favorable safety margin, with no significant adverse effects observed in animal models at therapeutic doses. However, comprehensive toxicological assessments are ongoing, including genotoxicity and chronic exposure studies, to fully characterize its safety profile before potential clinical applications.

In conclusion, 2-methyl-1-(propylsulfanyl)cyclobutane-1-carboxylic acid (CAS: 1504153-40-5) represents a promising compound with diverse applications in medicinal chemistry and drug development. Recent advances in its synthesis, biological evaluation, and formulation potential highlight its value as a research focus. As investigations continue, this compound may pave the way for novel therapeutic agents and delivery systems in the coming years. Researchers are encouraged to explore its full potential through collaborative efforts and interdisciplinary approaches.

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