3-Fluoro-5-methoxybenzeneboronic acid

98%

Reagent Code: #90173
label
Alias 3-Fluoro-5-methoxyphenylboronic acid;
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CAS Number 609807-25-2

science Other reagents with same CAS 609807-25-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.95 g/mol
Formula C₇H₈BFO₃
badge Registry Numbers
MDL Number MFCD07363780
thermostat Physical Properties
Melting Point 168-172°C(lit.)
Boiling Point 305.5ºC
inventory_2 Storage & Handling
Density 1.26g/cm3
Storage room temperature

description Product Description

Used primarily in organic synthesis, this compound serves as a key building block in the preparation of complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, enabling the creation of biaryl structures that are essential in pharmaceuticals and agrochemicals. Its fluorine and methoxy substituents enhance its reactivity and selectivity, making it valuable in the development of drug candidates and materials with specific electronic properties. Additionally, it finds application in the synthesis of advanced organic materials and liquid crystals, where precise molecular architecture is crucial.

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Test Parameter Specification
Purity 98-100%
Appearance White to off-white powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿340.00
inventory 5g
10-20 days ฿1,400.00
inventory 25g
10-20 days ฿5,247.00

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3-Fluoro-5-methoxybenzeneboronic acid
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Used primarily in organic synthesis, this compound serves as a key building block in the preparation of complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, enabling the creation of biaryl structures that are essential in pharmaceuticals and agrochemicals. Its fluorine and methoxy substituents enhance its reactivity and selectivity, making it valuable in the development of drug candidates and materials with specific electronic pr

Used primarily in organic synthesis, this compound serves as a key building block in the preparation of complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, enabling the creation of biaryl structures that are essential in pharmaceuticals and agrochemicals. Its fluorine and methoxy substituents enhance its reactivity and selectivity, making it valuable in the development of drug candidates and materials with specific electronic properties. Additionally, it finds application in the synthesis of advanced organic materials and liquid crystals, where precise molecular architecture is crucial.

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