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Sku CI17481_5_G
Chem Impex
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Product Information

Product Name
4-Bromothiazole
Brand Name
Chem Impex
Product Number
17481
CAS
34259-99-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2763218
IUPAC Name
4-bromo-1,3-thiazole
InChI Key
VDTIGYKLTROQAH-UHFFFAOYSA-N
SMILES
C1=C(N=CS1)Br

Application

4-Bromothiazole is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting bacterial and fungal infections.

Agricultural Chemicals: It is used in the formulation of agrochemicals, enhancing the efficacy of pesticides and herbicides, which help in improving crop yields.

Material Science: 4-Bromothiazole is employed in the development of novel materials, such as polymers and coatings, due to its unique chemical properties that improve durability and resistance.

Biochemical Research: Researchers utilize this compound in studies related to enzyme inhibition and receptor binding, aiding in the understanding of various biological processes.

Organic Synthesis: It acts as a versatile building block in organic synthesis, allowing chemists to create complex molecules efficiently, which is crucial in various industrial applications.

References Data Source From Pubchem

Recent advancements in the synthesis of bithiazole and its derivatives for versatile medicinal applications

Publication Name: Chemical Papers
Publication Date: 2025-09-02
DOI: 10.1007/s11696-025-04312-0

Fragment-Sized Thiazoles in Fragment-Based Drug Discovery Campaigns: Friend or Foe?

Publication Name: ACS Medicinal Chemistry Letters
Publication Date: 2022-11-03
DOI: 10.1021/acsmedchemlett.2c00429

The use of N-halosuccinimides for cyclization with the formation of five-membered heterocyclic compounds

Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2020-01
DOI: 10.1007/s10593-020-02616-5

Thiazoles and Benzothiazoles

Publication Name: Metalation of Azoles and Related Five-Membered Ring Heterocycles
Publication Date: 2012
DOI: 10.1007/7081_2012_78

Reactions of Primary Arylamines with Hetaryl Electrophiles

Publication Name: Science of Synthesis
Publication Date: 2012