(4-Amino-3-fluorophenyl)boronic acid

95%

Reagent Code: #138590
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CAS Number 494752-42-0

science Other reagents with same CAS 494752-42-0

blur_circular Chemical Specifications

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Weight 154.93 g/mol
Formula C₆H₇BNO₂F
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its fluorinated aromatic structure makes it valuable for creating bioactive molecules with enhanced metabolic stability and binding affinity. Commonly employed in the development of kinase inhibitors and other medicinal agents where fluorine substitution improves pharmacokinetic properties. Also utilized in materials science for designing fluorescent probes and functional polymers.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿660.00
inventory 250mg
10-20 days ฿1,200.00
inventory 1g
10-20 days ฿4,750.00
inventory 5g
10-20 days ฿20,600.00

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(4-Amino-3-fluorophenyl)boronic acid
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Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its fluorinated aromatic structure makes it valuable for creating bioactive molecules with enhanced metabolic stability and binding affinity. Commonly employed in the development of kinase inhibitors and other medicinal agents where fluorine substitution improves pharmacokinetic properties. Also utilized in materials science for designin

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its fluorinated aromatic structure makes it valuable for creating bioactive molecules with enhanced metabolic stability and binding affinity. Commonly employed in the development of kinase inhibitors and other medicinal agents where fluorine substitution improves pharmacokinetic properties. Also utilized in materials science for designing fluorescent probes and functional polymers.

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