Cas no 927983-00-4 (4-Methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid)

4-Methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid is a thiazole derivative with potential applications in pharmaceutical and agrochemical research. Its structural features, including the carboxylic acid and propylamino substituents, make it a versatile intermediate for synthesizing biologically active compounds. The thiazole core is known for its stability and ability to participate in diverse chemical reactions, facilitating further functionalization. This compound may exhibit favorable physicochemical properties, such as moderate solubility and reactivity, suitable for use in drug discovery or material science. Its precise molecular structure allows for targeted modifications, enhancing its utility in developing novel therapeutics or specialty chemicals.
4-Methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid structure
927983-00-4 structure
Product Name:4-Methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid
CAS No:927983-00-4
MF:C8H12N2O2S
MW:200.258080482483
CID:4720157
PubChem ID:9154586
Update Time:2025-06-13

4-Methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 4-methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid
    • 4-Methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid
    • Inchi: 1S/C8H12N2O2S/c1-3-4-9-8-10-5(2)6(13-8)7(11)12/h3-4H2,1-2H3,(H,9,10)(H,11,12)
    • InChI Key: AALKEOPFWFCWTN-UHFFFAOYSA-N
    • SMILES: S1C(C(=O)O)=C(C)N=C1NCCC

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 4
  • Complexity: 189
  • Topological Polar Surface Area: 90.5

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Additional information on 4-Methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid

Comprehensive Overview of 4-Methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid (CAS No. 927983-00-4)

4-Methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid (CAS No. 927983-00-4) is a specialized organic compound belonging to the thiazole family, a class of heterocyclic compounds known for their diverse applications in pharmaceuticals, agrochemicals, and material science. This compound features a carboxylic acid functional group, which enhances its reactivity and potential for derivatization, making it a valuable intermediate in synthetic chemistry. The presence of a propylamino substituent further contributes to its unique physicochemical properties, including solubility and bioavailability.

In recent years, the demand for thiazole derivatives has surged due to their role in drug discovery and development. Researchers are particularly interested in compounds like 4-Methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid for their potential as building blocks in the synthesis of bioactive molecules. For instance, thiazole-containing compounds have shown promise in targeting enzymes and receptors associated with inflammatory diseases, metabolic disorders, and even certain types of infections. This aligns with the growing trend of precision medicine and personalized therapeutics, where tailored molecular structures are designed to address specific biological pathways.

The compound's CAS No. 927983-00-4 is frequently searched in academic and industrial databases, reflecting its relevance in current chemical research. Users often inquire about its synthesis methods, spectroscopic data (such as NMR and IR spectra), and applications in medicinal chemistry. Additionally, questions about its stability under various conditions and compatibility with other reagents are common, highlighting the need for detailed technical documentation. These queries underscore the importance of structure-activity relationships (SAR) studies, which are critical for optimizing the compound's efficacy in target applications.

From an industrial perspective, 4-Methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid is also explored for its potential in green chemistry initiatives. With increasing emphasis on sustainable synthesis and eco-friendly processes, researchers are investigating catalytic methods to produce this compound with minimal waste and energy consumption. This aligns with global efforts to reduce the environmental footprint of chemical manufacturing, a topic gaining traction among policymakers and industry leaders.

Another area of interest is the compound's role in material science. Thiazole derivatives are known to exhibit unique electronic properties, making them candidates for organic semiconductors and photovoltaic materials. As the demand for renewable energy solutions grows, compounds like CAS No. 927983-00-4 could play a pivotal role in advancing next-generation solar cells and flexible electronics. This intersection of chemistry and technology is a hot topic in both academic and commercial circles.

In summary, 4-Methyl-2-(propylamino)-1,3-thiazole-5-carboxylic acid (CAS No. 927983-00-4) is a versatile compound with significant potential across multiple disciplines. Its applications in pharmaceuticals, green chemistry, and material science make it a subject of ongoing research and innovation. As scientific inquiry continues to evolve, this compound is likely to remain at the forefront of discussions about molecular design and functional materials.

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