Cas no 180597-84-6 (Thiazole, 5-(bromomethyl)-2,4-dimethyl-)

Thiazole, 5-(bromomethyl)-2,4-dimethyl-, is a brominated thiazole derivative characterized by its reactive bromomethyl group at the 5-position and methyl substituents at the 2- and 4-positions. This compound serves as a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and functional materials. The presence of the bromomethyl group enables facile nucleophilic substitution reactions, allowing for further functionalization. Its well-defined structure and high purity make it suitable for precise synthetic applications. The compound’s stability under standard conditions ensures reliable handling and storage, while its reactivity profile supports efficient derivatization in targeted chemical transformations.
Thiazole, 5-(bromomethyl)-2,4-dimethyl- structure
180597-84-6 structure
Product Name:Thiazole, 5-(bromomethyl)-2,4-dimethyl-
CAS No:180597-84-6
MF:C6H8BrNS
MW:206.103419303894
MDL:MFCD12756557
CID:5162346
PubChem ID:82425512
Update Time:2025-11-02

Thiazole, 5-(bromomethyl)-2,4-dimethyl- Chemical and Physical Properties

Names and Identifiers

    • Thiazole, 5-(bromomethyl)-2,4-dimethyl-
    • 5-bromomethyl-2,4-dimethyl-thiazole
    • MDL: MFCD12756557
    • Inchi: 1S/C6H8BrNS/c1-4-6(3-7)9-5(2)8-4/h3H2,1-2H3
    • InChI Key: ALLWWBUZTJULII-UHFFFAOYSA-N
    • SMILES: S1C(CBr)=C(C)N=C1C

Computed Properties

  • Exact Mass: 204.95608g/mol
  • Monoisotopic Mass: 204.95608g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 1
  • Complexity: 99.1
  • 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: 2.3
  • Topological Polar Surface Area: 41.1?2

Thiazole, 5-(bromomethyl)-2,4-dimethyl- Pricemore >>

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Additional information on Thiazole, 5-(bromomethyl)-2,4-dimethyl-

Comprehensive Guide to Thiazole, 5-(bromomethyl)-2,4-dimethyl- (CAS No. 180597-84-6): Properties, Applications, and Market Insights

Thiazole, 5-(bromomethyl)-2,4-dimethyl- (CAS No. 180597-84-6) is a specialized organic compound belonging to the thiazole family, known for its versatile applications in pharmaceuticals, agrochemicals, and material science. This brominated derivative of 2,4-dimethylthiazole has garnered significant attention due to its unique reactivity, making it a valuable intermediate in synthetic chemistry. In this article, we delve into the molecular structure, key properties, industrial uses, and emerging trends surrounding this compound, while addressing frequently asked questions by researchers and industry professionals.

The molecular formula of 5-(bromomethyl)-2,4-dimethylthiazole is C6H8BrNS, with a molecular weight of 206.10 g/mol. Its structure features a thiazole ring—a five-membered heterocycle containing sulfur and nitrogen atoms—substituted with methyl groups at positions 2 and 4, and a reactive bromomethyl group at position 5. This configuration enables diverse chemical transformations, particularly in nucleophilic substitution reactions, which are pivotal for creating complex molecules in drug discovery and specialty chemicals.

One of the most searched questions about CAS 180597-84-6 relates to its synthetic utility. Researchers frequently explore how this compound serves as a building block for biologically active molecules. For instance, the bromomethyl group can be easily functionalized to introduce amines, alcohols, or other heteroatoms, making it indispensable in designing pharmaceutical intermediates. Recent studies highlight its role in developing kinase inhibitors and antimicrobial agents, aligning with the growing demand for novel therapeutics in precision medicine.

In agrochemical applications, 5-(bromomethyl)-2,4-dimethylthiazole has been investigated as a precursor for crop protection agents. Its derivatives show potential in creating fungicides and herbicides with enhanced efficacy and environmental safety—a hot topic in sustainable agriculture. Industry reports indicate rising interest in thiazole-based agrochemicals due to their target specificity and lower ecological impact compared to traditional pesticides.

Material scientists are also exploring CAS 180597-84-6 for advanced applications. The compound’s ability to form stable coordination complexes with metals makes it relevant in designing organic electronic materials, such as OLEDs and conductive polymers. With the global push toward renewable energy and smart devices, this aspect of thiazole chemistry is gaining traction in R&D circles.

From a commercial perspective, the market for 2,4-dimethyl-5-(bromomethyl)thiazole is influenced by regional regulatory policies and supply chain dynamics. Analytical data suggests steady growth in demand from Asia-Pacific pharmaceutical hubs, driven by increased outsourcing of drug intermediate synthesis. Quality standards like HPLC purity (>98%) and stringent storage conditions (under inert atmosphere) are critical purchase considerations for bulk buyers.

Environmental and handling aspects of 180597-84-6 frequently appear in search queries. While not classified as hazardous under major regulatory frameworks, proper lab practices—including the use of PPE and ventilation—are recommended when handling this brominated compound. Disposal should follow institutional guidelines for halogenated waste, reflecting the chemical industry’s focus on green chemistry principles.

Innovation trends surrounding thiazole derivatives continue to evolve. Patent analyses reveal growing applications in battery electrolytes and corrosion inhibitors, particularly in electric vehicle components. Researchers are optimizing synthetic routes to 5-(bromomethyl)-2,4-dimethylthiazole using catalytic methods to improve atom economy—a response to the pharmaceutical industry’s emphasis on sustainable manufacturing.

For those sourcing CAS 180597-84-6, technical specifications typically include: white to pale yellow crystalline appearance, melting point range of 45-48°C, and solubility in common organic solvents (e.g., DCM, THF). Suppliers often provide customized packaging options from gram-scale for research to kilogram quantities for industrial use, with documentation including COA, MSDS, and NMR spectra.

In conclusion, Thiazole, 5-(bromomethyl)-2,4-dimethyl- represents a multifaceted compound bridging multiple industries. Its chemical versatility addresses key challenges in drug development, sustainable agriculture, and advanced materials—all priority areas in global R&D investments. As synthetic methodologies advance and application scope expands, this brominated thiazole derivative is poised to remain a compound of significant scientific and commercial interest.

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