4-Bromo-2-(trifluoromethyl)benzo[d]thiazole

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Reagent Code: #87001
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CAS Number 1188136-39-1

science Other reagents with same CAS 1188136-39-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.08 g/mol
Formula C₈H₃BrF₃NS
badge Registry Numbers
MDL Number MFCD11217356
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique combination of bromine and trifluoromethyl groups on the benzo[d]thiazole ring makes it particularly valuable in the creation of pharmaceuticals, agrochemicals, and advanced materials. In medicinal chemistry, it serves as a key intermediate for designing molecules with potential biological activity, such as enzyme inhibitors or receptor modulators. Additionally, its electron-withdrawing properties are exploited in the synthesis of dyes, fluorescent markers, and other functional materials. The compound's stability and reactivity also make it suitable for use in cross-coupling reactions, enabling the construction of diverse aromatic systems.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿37,359.00
inventory 100mg
10-20 days ฿8,145.00
inventory 250mg
10-20 days ฿13,842.00

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4-Bromo-2-(trifluoromethyl)benzo[d]thiazole
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This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique combination of bromine and trifluoromethyl groups on the benzo[d]thiazole ring makes it particularly valuable in the creation of pharmaceuticals, agrochemicals, and advanced materials. In medicinal chemistry, it serves as a key intermediate for designing molecules with potential biological activity, such as enzyme inhibitors or receptor modulators. Add

This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique combination of bromine and trifluoromethyl groups on the benzo[d]thiazole ring makes it particularly valuable in the creation of pharmaceuticals, agrochemicals, and advanced materials. In medicinal chemistry, it serves as a key intermediate for designing molecules with potential biological activity, such as enzyme inhibitors or receptor modulators. Additionally, its electron-withdrawing properties are exploited in the synthesis of dyes, fluorescent markers, and other functional materials. The compound's stability and reactivity also make it suitable for use in cross-coupling reactions, enabling the construction of diverse aromatic systems.

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