(3-Bromo-2,5-dimethylphenyl)boronic acid

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Reagent Code: #117970
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CAS Number 1259318-83-6

science Other reagents with same CAS 1259318-83-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.88 g/mol
Formula C₈H₁₀BBrO₂
badge Registry Numbers
MDL Number MFCD12026703
thermostat Physical Properties
Boiling Point 363.3±52.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

(3-Bromo-2,5-dimethylphenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate in cross-coupling reactions, such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules, including potential drug candidates. Its boronic acid group facilitates the formation of biaryl structures, which are common in many biologically active compounds. Additionally, it is used in material science for the development of organic electronic materials, where precise molecular architecture is crucial. The compound’s bromo and methyl substituents further enhance its reactivity and selectivity in various chemical transformations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿693.00
inventory 100mg
10-20 days ฿369.00

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(3-Bromo-2,5-dimethylphenyl)boronic acid
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(3-Bromo-2,5-dimethylphenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate in cross-coupling reactions, such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules, including potential drug candidates. Its boronic acid group facilitates the formation of biaryl structures, which are common in many biologically active compounds. Additionally, it is

(3-Bromo-2,5-dimethylphenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate in cross-coupling reactions, such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules, including potential drug candidates. Its boronic acid group facilitates the formation of biaryl structures, which are common in many biologically active compounds. Additionally, it is used in material science for the development of organic electronic materials, where precise molecular architecture is crucial. The compound’s bromo and methyl substituents further enhance its reactivity and selectivity in various chemical transformations.

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