(4-(Benzyloxy)-2,3-difluorophenyl)boronic acid

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Reagent Code: #119632
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CAS Number 156635-87-9

science Other reagents with same CAS 156635-87-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.03 g/mol
Formula C₁₃H₁₁BF₂O₃
badge Registry Numbers
MDL Number MFCD07644469
thermostat Physical Properties
Boiling Point 417.3±55.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of drug candidates. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, such as those used in cancer research and other therapeutic areas. Additionally, it may be employed in material science for creating advanced polymers or organic electronic materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿7,434.00
inventory 100mg
10-20 days ฿495.00
inventory 250mg
10-20 days ฿747.00
inventory 1g
10-20 days ฿1,845.00

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(4-(Benzyloxy)-2,3-difluorophenyl)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 for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of drug candidates. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, such as those used in cancer researc

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of drug candidates. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, such as those used in cancer research and other therapeutic areas. Additionally, it may be employed in material science for creating advanced polymers or organic electronic materials.

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