4-Acetylphenylboronic acid

98%

Reagent Code: #90554
label
Alias 4-Acetophenylboronic acid
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CAS Number 149104-90-5

science Other reagents with same CAS 149104-90-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.97 g/mol
Formula C₈H₉BO₃
badge Registry Numbers
MDL Number MFCD01074667
thermostat Physical Properties
Melting Point 240-244 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules. Additionally, it finds application in the development of sensors and diagnostic agents due to its ability to interact with diols and sugars, making it useful in glucose sensing technologies. Its boronic acid group also allows for its use in materials science, particularly in the creation of advanced polymers and coatings with specific functional properties.

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Test Parameter Specification
Melting Point 243-247
Purity 98-100
Appearance White to off-white powder, crystals and/or chunks

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿320.00
inventory 5g
10-20 days ฿990.00
inventory 25g
10-20 days ฿3,780.00

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4-Acetylphenylboronic acid
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Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules. Additionally, it finds application in the development of sensors and diagnostic agents due to its ability to interact with diols and sugars, making it useful in glucose sensing tec

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules. Additionally, it finds application in the development of sensors and diagnostic agents due to its ability to interact with diols and sugars, making it useful in glucose sensing technologies. Its boronic acid group also allows for its use in materials science, particularly in the creation of advanced polymers and coatings with specific functional properties.

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