Cas no 16585-37-8 (5-Isopropylthiazole)

5-Isopropylthiazole is a heterocyclic organic compound featuring a thiazole ring substituted with an isopropyl group at the 5-position. This compound is primarily utilized as a flavor and fragrance intermediate, contributing to the synthesis of compounds with earthy, green, or nutty aromatic profiles. Its structural stability and reactivity make it a valuable building block in organic synthesis, particularly for agrochemicals and pharmaceuticals. The isopropyl group enhances lipophilicity, improving solubility in nonpolar matrices. 5-Isopropylthiazole is characterized by its high purity and consistent performance, ensuring reproducibility in industrial applications. Proper handling is advised due to its potential volatility and sensitivity to light and moisture.
5-Isopropylthiazole structure
5-Isopropylthiazole structure
Product Name:5-Isopropylthiazole
CAS No:16585-37-8
MF:C6H9NS
MW:127.207360029221
MDL:MFCD23701490
CID:1037182
PubChem ID:18736806
Update Time:2025-10-28

5-Isopropylthiazole Chemical and Physical Properties

Names and Identifiers

    • 5-Isopropylthiazole
    • 5-propan-2-yl-1,3-thiazole
    • 5-i-propyl-thiazol
    • 5-Isopropylthiazol
    • 5-isopropyl-thiazole
    • AK109748
    • CTK0E5676
    • KB-246286
    • SureCN84600
    • Thiazole, 5-(1-methylethyl)-
    • 5-ISOPROPYL-1,3-THIAZOLE
    • EN300-734627
    • DTXSID90595894
    • DB-368748
    • CS-0259471
    • 5-isopropyl thiazole
    • SCHEMBL84600
    • 5-(Propan-2-yl)-1,3-thiazole
    • 16585-37-8
    • MDL: MFCD23701490
    • Inchi: 1S/C6H9NS/c1-5(2)6-3-7-4-8-6/h3-5H,1-2H3
    • InChI Key: GUCKIHDYYQOYJB-UHFFFAOYSA-N
    • SMILES: S1C=NC=C1C(C)C

Computed Properties

  • Exact Mass: 127.04567
  • Monoisotopic Mass: 127.04557046g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 1
  • Complexity: 72.9
  • 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: 2.1
  • Topological Polar Surface Area: 41.1?2

Experimental Properties

  • PSA: 12.89

5-Isopropylthiazole Pricemore >>

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Additional information on 5-Isopropylthiazole

Exploring 5-Isopropylthiazole (CAS No. 16585-37-8): Properties, Applications, and Industry Trends

5-Isopropylthiazole (CAS No. 16585-37-8) is a versatile organic compound belonging to the thiazole family, renowned for its unique aromatic and heterocyclic structure. This compound has garnered significant attention in industries ranging from flavor and fragrance to pharmaceutical intermediates. With a molecular formula of C6H9NS, it exhibits a distinct sulfurous and herbaceous odor, making it a valuable ingredient in synthetic formulations. Below, we delve into its properties, applications, and relevance in modern research.

The chemical structure of 5-Isopropylthiazole features a thiazole ring substituted with an isopropyl group at the fifth position. This configuration contributes to its stability and reactivity, enabling diverse functional roles. In the flavor industry, it is prized for its ability to mimic natural green notes, often found in vegetables like tomatoes and bell peppers. As consumers increasingly demand clean-label and plant-based products, 5-Isopropylthiazole serves as a sustainable alternative to traditional extracts.

Recent advancements in synthetic chemistry have expanded the utility of 5-Isopropylthiazole in agrochemicals and material science. Researchers are exploring its potential as a building block for bioactive molecules, particularly in crop protection formulations. Its compatibility with green chemistry principles aligns with global trends toward eco-friendly solutions, addressing concerns about environmental impact and regulatory compliance.

From a commercial perspective, the demand for 5-Isopropylthiazole is driven by its cost-effectiveness and scalability. Manufacturers are optimizing production processes to meet the needs of high-volume applications, such as food additives and cosmetic enhancers. Analytical techniques like GC-MS and NMR spectroscopy ensure stringent quality control, critical for maintaining consumer safety and industry standards.

In the context of market trends, 5-Isopropylthiazole is frequently searched alongside terms like "thiazole derivatives uses" and "synthetic flavors for food." These queries reflect growing interest in specialty chemicals and innovative formulations. Additionally, its role in vegan-friendly products resonates with the health-conscious demographic, further boosting its relevance.

Looking ahead, 5-Isopropylthiazole is poised to play a pivotal role in next-generation applications. Collaborative research between academia and industry is uncovering novel uses, such as smart packaging materials and controlled-release systems. As regulatory frameworks evolve, stakeholders must prioritize transparency and sustainability to capitalize on emerging opportunities.

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