2,5-Dibromo-4-fluorobenzo[d]thiazole

95%

Reagent Code: #175047
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CAS Number 1427426-59-2

science Other reagents with same CAS 1427426-59-2

blur_circular Chemical Specifications

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Weight 310.97 g/mol
Formula C₇H₂Br₂FNS
inventory_2 Storage & Handling
Storage -20℃

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its halogenated structure makes it suitable for cross-coupling reactions, particularly in the development of bioactive molecules. Commonly employed in the preparation of fluorescent dyes and optoelectronic materials due to the benzo[d]thiazole core’s electron-accepting properties. Also explored in the synthesis of kinase inhibitors and antimicrobial agents. The presence of bromine and fluorine atoms allows for selective functionalization, enabling fine-tuning of molecular properties in drug discovery and material science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿900.00
inventory 500mg
10-20 days ฿4,390.00
inventory 1g
10-20 days ฿8,540.00

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2,5-Dibromo-4-fluorobenzo[d]thiazole
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its halogenated structure makes it suitable for cross-coupling reactions, particularly in the development of bioactive molecules. Commonly employed in the preparation of fluorescent dyes and optoelectronic materials due to the benzo[d]thiazole core’s electron-accepting properties. Also explored in the synthesis of kinase inhibitors and antimicrobial agents. The presence of bromine and fluorine atoms allows for selective f

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its halogenated structure makes it suitable for cross-coupling reactions, particularly in the development of bioactive molecules. Commonly employed in the preparation of fluorescent dyes and optoelectronic materials due to the benzo[d]thiazole core’s electron-accepting properties. Also explored in the synthesis of kinase inhibitors and antimicrobial agents. The presence of bromine and fluorine atoms allows for selective functionalization, enabling fine-tuning of molecular properties in drug discovery and material science.

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