Cas no 24383-50-4 (3-(Isopropylthio)propanoic acid)

3-(Isopropylthio)propanoic acid is a sulfur-containing carboxylic acid derivative characterized by its isopropylthio functional group. This compound is primarily utilized as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its thioether linkage enhances reactivity in nucleophilic substitution and addition reactions, while the carboxylic acid group allows for further functionalization. The isopropyl substituent contributes to steric and electronic modulation, influencing selectivity in synthetic pathways. The compound exhibits moderate stability under standard conditions, making it suitable for controlled reaction environments. Its balanced lipophilicity and reactivity profile render it valuable in the design of bioactive molecules and fine chemical applications.
3-(Isopropylthio)propanoic acid structure
24383-50-4 structure
Product Name:3-(Isopropylthio)propanoic acid
CAS No:24383-50-4
MF:C6H12O2S
MW:148.223280906677
CID:274649
PubChem ID:222478
Update Time:2025-06-12

3-(Isopropylthio)propanoic acid Chemical and Physical Properties

Names and Identifiers

    • Propanoic acid,3-[(1-methylethyl)thio]-
    • 3-propan-2-ylsulfanylpropanoic acid
    • 3-(isopropylsulfanyl)-propanoic acid
    • 3-(isopropylthio)propionic acid
    • 3-(propan-2-ylsulfanyl)propanoic acid
    • 3-Isopropylmercapto-propionsaeure
    • AC1L5BTL
    • AC1Q5WG5
    • CTK4F3529
    • NSC8523
    • Propionic acid, 3-(isopropylthio)-
    • Propanoic acid, 3-[(1-methylethyl)thio]-
    • 24383-50-4
    • SCHEMBL7276318
    • DTXSID10278617
    • AKOS000180391
    • BSMZRZIXCAUUCT-UHFFFAOYSA-N
    • NSC-8523
    • 3-(Isopropylsulfanyl)propanoic acid #
    • A1-08075
    • 3-(Isopropylthio)propanoic acid
    • Inchi: 1S/C6H12O2S/c1-5(2)9-4-3-6(7)8/h5H,3-4H2,1-2H3,(H,7,8)
    • InChI Key: BSMZRZIXCAUUCT-UHFFFAOYSA-N
    • SMILES: S(CCC(=O)O)C(C)C

Computed Properties

  • Exact Mass: 148.05586
  • Monoisotopic Mass: 148.05580079g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 4
  • Complexity: 91.1
  • 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: 1.2
  • Topological Polar Surface Area: 62.6?2

Experimental Properties

  • PSA: 37.3

3-(Isopropylthio)propanoic acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
I184905-125mg
3-(Isopropylthio)propanoic acid
24383-50-4
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$ 440.00 2022-06-04
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$ 730.00 2022-06-04
A2B Chem LLC
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A2B Chem LLC
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Additional information on 3-(Isopropylthio)propanoic acid

Recent Advances in the Study of 3-(Isopropylthio)propanoic acid (CAS: 24383-50-4) in Chemical Biology and Pharmaceutical Research

3-(Isopropylthio)propanoic acid (CAS: 24383-50-4) is a sulfur-containing organic compound that has garnered significant attention in recent years due to its potential applications in chemical biology and pharmaceutical research. This compound, characterized by its unique isopropylthio moiety, has been explored for its role in various biochemical pathways and as a building block for more complex molecules. Recent studies have highlighted its utility in drug design, enzyme inhibition, and as a precursor for bioactive molecules, making it a compound of interest for researchers in the field.

One of the key areas of research involving 3-(Isopropylthio)propanoic acid is its potential as a modulator of enzyme activity. A 2023 study published in the Journal of Medicinal Chemistry demonstrated that derivatives of this compound exhibit inhibitory effects on specific enzymes involved in inflammatory pathways. The study utilized molecular docking and kinetic assays to elucidate the binding mechanisms, revealing that the isopropylthio group plays a critical role in stabilizing the enzyme-inhibitor complex. These findings suggest that 3-(Isopropylthio)propanoic acid could serve as a scaffold for developing novel anti-inflammatory agents.

In addition to its enzyme-modulating properties, 3-(Isopropylthio)propanoic acid has also been investigated for its role in prodrug design. A recent preprint on bioRxiv detailed the synthesis of prodrugs incorporating this compound, which showed enhanced bioavailability and targeted delivery in preclinical models. The researchers employed advanced spectroscopic techniques, including NMR and mass spectrometry, to confirm the structural integrity of the prodrugs and their metabolites. This study underscores the compound's versatility in improving drug delivery systems, particularly for poorly soluble therapeutics.

Another notable application of 3-(Isopropylthio)propanoic acid is in the field of chemical proteomics. A 2024 publication in Nature Chemical Biology reported the use of this compound as a chemical probe to identify novel protein targets in cancer cells. The study combined activity-based protein profiling (ABPP) with quantitative proteomics to map the interaction network of the probe, revealing previously unknown protein-ligand interactions. This approach opens new avenues for target discovery and validation in oncology research.

Despite these promising developments, challenges remain in the widespread adoption of 3-(Isopropylthio)propanoic acid in pharmaceutical applications. Issues such as synthetic scalability, metabolic stability, and potential off-target effects need to be addressed through further research. However, the compound's unique chemical properties and demonstrated bioactivity make it a valuable tool for advancing our understanding of biochemical processes and developing next-generation therapeutics.

In conclusion, 3-(Isopropylthio)propanoic acid (CAS: 24383-50-4) represents a versatile and promising compound in chemical biology and pharmaceutical research. Recent studies have elucidated its potential in enzyme inhibition, prodrug design, and chemical proteomics, highlighting its broad applicability. As research continues to uncover new insights into its mechanisms and applications, this compound is poised to play an increasingly important role in drug discovery and development.

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