3-Borono-5-bromo-2-fluorobenzoic acid

97%

Reagent Code: #148164
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CAS Number 957120-63-7

science Other reagents with same CAS 957120-63-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.83 g/mol
Formula C₇H₅BBrFO₄
badge Registry Numbers
MDL Number MFCD09800869
thermostat Physical Properties
Boiling Point 463.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl structures found in active drug molecules. Also applied in medicinal chemistry research for designing protease inhibitors and other bioactive agents. The presence of halogen and fluorine atoms allows further functionalization and enhances binding selectivity in target proteins.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,050.00
5g
10-20 days ฿4,700.00
10g
10-20 days ฿8,920.00
50g
10-20 days ฿27,890.00
3-Borono-5-bromo-2-fluorobenzoic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl structures found in active drug molecules. Also applied in medicinal chemistry research for designing protease inhibitors and other bioactive agents. The presence of halogen and fluorine atoms allows further functionalization and enhances binding sel

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl structures found in active drug molecules. Also applied in medicinal chemistry research for designing protease inhibitors and other bioactive agents. The presence of halogen and fluorine atoms allows further functionalization and enhances binding selectivity in target proteins.

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