(4-(2-Hydroxyethyl)phenyl)boronic acid

97%

Reagent Code: #113260
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CAS Number 137756-89-9

science Other reagents with same CAS 137756-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.98 g/mol
Formula C₈H₁₁BO₃
badge Registry Numbers
MDL Number MFCD03095135
thermostat Physical Properties
Boiling Point 359.9°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, where it acts as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables it to react with aryl halides in the presence of a palladium catalyst, making it valuable for constructing complex organic molecules, such as pharmaceuticals and advanced materials. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and sugars, making it useful in biochemical research and diagnostic applications. Its hydroxyethyl group also enhances solubility and reactivity in aqueous environments, broadening its utility in various chemical processes.

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Test Parameter Specification
Appearance Off-white Powder
Purity (%) 96.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,319.00
inventory 5g
10-20 days ฿40,095.00
inventory 100mg
10-20 days ฿3,339.00
inventory 1g
10-20 days ฿13,338.00

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(4-(2-Hydroxyethyl)phenyl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables it to react with aryl halides in the presence of a palladium catalyst, making it valuable for constructing complex organic molecules, such as pharmaceuticals and advanced materials. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and s

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables it to react with aryl halides in the presence of a palladium catalyst, making it valuable for constructing complex organic molecules, such as pharmaceuticals and advanced materials. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and sugars, making it useful in biochemical research and diagnostic applications. Its hydroxyethyl group also enhances solubility and reactivity in aqueous environments, broadening its utility in various chemical processes.

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