7-Bromo-2-chloro-6-methoxybenzo[d]thiazole

≥95%

Reagent Code: #51844
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CAS Number 911056-05-8

science Other reagents with same CAS 911056-05-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.55 g/mol
Formula C₈H₅BrClNOS
badge Registry Numbers
MDL Number MFCD12827957
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both bromo and chloro substituents, makes it particularly valuable for constructing complex molecules through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Additionally, the methoxy group enhances its reactivity and selectivity in these processes. It is also employed in the development of bioactive compounds, including potential drug candidates targeting specific enzymes or receptors. Its applications extend to material science, where it contributes to the synthesis of advanced organic materials with tailored properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,830.00
250mg
10-20 days ฿15,660.00
7-Bromo-2-chloro-6-methoxybenzo[d]thiazole
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This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both bromo and chloro substituents, makes it particularly valuable for constructing complex molecules through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Additionally, the methoxy group enhances its reactivity and selectivity in these processes. It is also employed in the dev

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both bromo and chloro substituents, makes it particularly valuable for constructing complex molecules through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Additionally, the methoxy group enhances its reactivity and selectivity in these processes. It is also employed in the development of bioactive compounds, including potential drug candidates targeting specific enzymes or receptors. Its applications extend to material science, where it contributes to the synthesis of advanced organic materials with tailored properties.

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