(2-((tert-Butoxycarbonyl)amino)-7-fluorobenzo[d]thiazol-4-yl)boronic acid

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Reagent Code: #88996
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CAS Number 2415163-55-0

science Other reagents with same CAS 2415163-55-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.12 g/mol
Formula C₁₂H₁₄BFN₂O₄S
badge Registry Numbers
MDL Number MFCD32689945
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the preparation of complex molecules, especially in the pharmaceutical industry. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biologically active compounds. The fluorobenzo[d]thiazole moiety is often incorporated into drug candidates targeting various diseases, including cancer and neurological disorders. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective modifications during multi-step synthetic processes, enhancing its versatility in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,065.00
inventory 250mg
10-20 days ฿10,620.00
inventory 1g
10-20 days ฿26,640.00
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(2-((tert-Butoxycarbonyl)amino)-7-fluorobenzo[d]thiazol-4-yl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the preparation of complex molecules, especially in the pharmaceutical industry. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biologically active compounds. The fluorobenzo[d]thiazole moiety is often incorporated into drug candidates targeting various diseases, including cancer and neurological dis

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the preparation of complex molecules, especially in the pharmaceutical industry. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biologically active compounds. The fluorobenzo[d]thiazole moiety is often incorporated into drug candidates targeting various diseases, including cancer and neurological disorders. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective modifications during multi-step synthetic processes, enhancing its versatility in medicinal chemistry research.

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