4-(Bromomethyl)-2-methylthiazole hydrobromide

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Reagent Code: #118733
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CAS Number 725738-57-8

science Other reagents with same CAS 725738-57-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.99 g/mol
Formula C₅H₇Br₂NS
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its bromomethyl group makes it highly reactive, enabling it to participate in nucleophilic substitution reactions, which are essential for constructing complex molecular structures. In medicinal chemistry, it is often employed in the development of thiazole-containing drugs, which are known for their antimicrobial, anti-inflammatory, and anticancer properties. Additionally, it finds utility in the synthesis of fungicides and herbicides, contributing to advancements in crop protection and agricultural productivity. Its role in facilitating the introduction of thiazole rings into target molecules makes it a valuable tool in research and industrial applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,380.00
inventory 50mg
10-20 days ฿3,030.00

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4-(Bromomethyl)-2-methylthiazole hydrobromide
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its bromomethyl group makes it highly reactive, enabling it to participate in nucleophilic substitution reactions, which are essential for constructing complex molecular structures. In medicinal chemistry, it is often employed in the development of thiazole-containing drugs, which are known for their antimicrobial, anti-inflammatory, and anticancer properties. Ad

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its bromomethyl group makes it highly reactive, enabling it to participate in nucleophilic substitution reactions, which are essential for constructing complex molecular structures. In medicinal chemistry, it is often employed in the development of thiazole-containing drugs, which are known for their antimicrobial, anti-inflammatory, and anticancer properties. Additionally, it finds utility in the synthesis of fungicides and herbicides, contributing to advancements in crop protection and agricultural productivity. Its role in facilitating the introduction of thiazole rings into target molecules makes it a valuable tool in research and industrial applications.

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