5-Fluoro-2-methoxybenzeneboronic acid

97%

Reagent Code: #90885
label
Alias 5-fluoro-2-methoxyphenylboronic acid
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CAS Number 179897-94-0

science Other reagents with same CAS 179897-94-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.95 g/mol
Formula C₇H₈BFO₃
badge Registry Numbers
MDL Number MFCD01863526
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of drugs targeting cancer and other diseases. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. This chemical is also employed in the production of agrochemicals and materials for organic electronics. Its boronic acid group makes it valuable in bioconjugation and sensing applications, where it can selectively bind to diols and other biomolecules. Additionally, it is utilized in research for developing novel therapeutic agents and diagnostic tools.

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Test Parameter Specification
Purity (GC) 97-100%
Melting point 144-153
Appearance White crystal
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿390.00
inventory 5g
10-20 days ฿1,190.00
inventory 25g
10-20 days ฿4,940.00

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5-Fluoro-2-methoxybenzeneboronic acid
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Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of drugs targeting cancer and other diseases. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. This chemical is also employed in the production of agrochemicals and materials for organic electronics. Its boronic acid group makes it valuable in bioconjugation and sensing applications, where it

Used as a key intermediate in the synthesis of various pharmaceutical compounds, particularly in the development of drugs targeting cancer and other diseases. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. This chemical is also employed in the production of agrochemicals and materials for organic electronics. Its boronic acid group makes it valuable in bioconjugation and sensing applications, where it can selectively bind to diols and other biomolecules. Additionally, it is utilized in research for developing novel therapeutic agents and diagnostic tools.

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