108306-63-4

Usage

Uses

Used in Pharmaceutical Industry:
2-BROMO-5-IODOTHIAZOLE is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs due to its unique structural properties that can be incorporated into medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 2-BROMO-5-IODOTHIAZOLE is utilized as a key intermediate in the creation of agrochemicals, potentially enhancing crop protection and management through novel chemical entities.
Used in Organic Synthesis:
2-BROMO-5-IODOTHIAZOLE serves as a versatile intermediate in organic synthesis, allowing for the construction of complex organic molecules for a wide array of applications, including the development of new materials and compounds.
Used in Research:
2-BROMO-5-IODOTHIAZOLE is also used in research settings as a model or reagent to explore new chemical reactions and mechanisms, furthering scientific understanding and innovation in the field of chemistry.
It is crucial to handle 2-BROMO-5-IODOTHIAZOLE with care, adhering to safety protocols and guidelines to ensure safe usage in all applications.

InChI:InChI=1/C3HBrINS/c4-3-6-1-2(5)7-3/h1H

Upstream product

• 79265-30-8 2-(trimethylsilyl)thiazole 
• 3034-53-5 2-bromo-1,3-thiazole 

Relevant academic research and scientific papers

Halogenated 2′-chlorobithiazoles via Pd-catalyzed cross-coupling reactions

Halogenated bithiazoles allow facile further functionalization and are, therefore, suitable intermediates for the synthesis of compounds with interesting biological activity or material science properties. The applicability of three coupling methods (Negi

BISAMID-ZINKBASEN

The present invention relates to zinc amide bases of the general formula (I) [in-line-formulae](R1R2N)2—Zn.aMgX12.bLiX2??(I)[/in-line-formulae] wherein R1 and R2 are e

(tmp)2Zn·2 MgCl2·2 LiCl: A chemoselective base for the directed zincation of sensitive arenes and heteroarenes

(Chemical Equation Presented) Positive zincing: A wide range of polyfunctional aryl and heteroaryl zinc reagents were efficiently prepared in THF by direct zincation using (tmp)2Zn·2 MgCl 2·2 LiCl (1), an exceptionally active base. Ester and cyano functions as well as aldehydes and nitro groups are tolerated. dba = dibenzylideneacetone, tmp = 2,2,6,6-tetramethylpiperidide.

Synthesis of Stannylthiazoles and Mixed Stannylsilylthiazoles and their Use for a Convenient Preparation of Mono- and Bis-halothiazoles

Stannylthiazoles and stannyl-silylthiazoles have been prepared and employed as thiazolyl carbanion equivalents in reactions with halogens to give mono- and mixed bis-halothiazoles in good yields.