(4-Bromonaphthalen-1-yl)boronic acid

≥98%

Reagent Code: #90655
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CAS Number 145965-14-6

science Other reagents with same CAS 145965-14-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.88 g/mol
Formula C₁₀H₈BBrO₂
thermostat Physical Properties
Melting Point 230-260 °C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in cross-coupling reactions, such as Suzuki-Miyaura coupling. It facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its application is significant in pharmaceutical research, where it aids in the development of drug candidates. Additionally, it is employed in material science for the synthesis of organic electronic materials, contributing to advancements in OLEDs and other optoelectronic devices. The compound's boronic acid group is crucial for its reactivity, making it a valuable tool in various chemical transformations.

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Test Parameter Specification
Appearance White to Off-white Solid
Purity (%) 98-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿1,287.00

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(4-Bromonaphthalen-1-yl)boronic acid
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Used primarily in organic synthesis, this compound serves as a key intermediate in cross-coupling reactions, such as Suzuki-Miyaura coupling. It facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its application is significant in pharmaceutical research, where it aids in the development of drug candidates. Additionally, it is employed in material science for the synthesis of organic electronic materials, contributing to advancements in OLEDs and other optoelectronic devices. The compound's boronic acid group is crucial for its reactivity, making it a valuable tool in various chemical transformations.
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