(2-Fluoro-3-iodophenyl)boronic acid

97%

Reagent Code: #67372
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CAS Number 1016231-39-2

science Other reagents with same CAS 1016231-39-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.82 g/mol
Formula C₆H₅BFIO₂
thermostat Physical Properties
Melting Point 238-243°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(2-Fluoro-3-iodophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound's unique structure, featuring both fluorine and iodine substituents, allows for selective functionalization, enabling the creation of complex molecules. It is also employed in the development of boron-based drugs and as a building block in medicinal chemistry for designing bioactive compounds. Additionally, its utility extends to material science, where it contributes to the synthesis of organic electronic materials and polymers.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿648.00
250mg
10-20 days ฿288.00
5g
10-20 days ฿2,637.00
(2-Fluoro-3-iodophenyl)boronic acid
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(2-Fluoro-3-iodophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound's unique structure, featuring both fluorine and iodine substituents, allows for selective functionalization, enabling the creation of complex molecules. It is also employed in the development of boron-based drugs and as a building block in medicinal chemistry for designing bioactive compounds. Additionally, its utility extends to material science, where it contributes to the synthesis of organic electronic materials and polymers.
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