4-Bromo-2-methylbenzo[d]thiazole

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Reagent Code: #146205
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CAS Number 112146-10-8

science Other reagents with same CAS 112146-10-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.11 g/mol
Formula C₈H₆BrNS
badge Registry Numbers
MDL Number MFCD11217352
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in the development of bioactive molecules. Its structure supports the formation of thiazole-based derivatives, which are common in drugs with antimicrobial, anti-inflammatory, and anticancer properties. It is also employed in the preparation of fluorescent dyes and optoelectronic materials due to the electron-rich nature of the benzothiazole core. In research, it serves as a building block for constructing complex heterocyclic systems through cross-coupling reactions, particularly in palladium-catalyzed transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,450.00
inventory 250mg
10-20 days ฿2,220.00

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4-Bromo-2-methylbenzo[d]thiazole
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in the development of bioactive molecules. Its structure supports the formation of thiazole-based derivatives, which are common in drugs with antimicrobial, anti-inflammatory, and anticancer properties. It is also employed in the preparation of fluorescent dyes and optoelectronic materials due to the electron-rich nature of the benzothiazole core. In research, it serves as a building bl

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in the development of bioactive molecules. Its structure supports the formation of thiazole-based derivatives, which are common in drugs with antimicrobial, anti-inflammatory, and anticancer properties. It is also employed in the preparation of fluorescent dyes and optoelectronic materials due to the electron-rich nature of the benzothiazole core. In research, it serves as a building block for constructing complex heterocyclic systems through cross-coupling reactions, particularly in palladium-catalyzed transformations.

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