(4-(Benzyloxy)-2,6-dimethylphenyl)boronic acid

≥95%

Reagent Code: #115521
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CAS Number 865139-18-0

science Other reagents with same CAS 865139-18-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.11 g/mol
Formula C₁₅H₁₇BO₃
badge Registry Numbers
MDL Number MFCD13194673
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

(4-(Benzyloxy)-2,6-dimethylphenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry for the construction of biaryl compounds, which are essential building blocks in the development of various drugs and bioactive molecules. The compound serves as a key intermediate, enabling the formation of carbon-carbon bonds between aryl groups, a critical step in synthesizing complex organic molecules. Additionally, its boronic acid group makes it valuable in the preparation of sensors and probes for detecting specific analytes in biochemical research. Its application extends to materials science, where it contributes to the development of advanced polymers and organic electronic materials.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,485.00
inventory 250mg
10-20 days ฿495.00

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(4-(Benzyloxy)-2,6-dimethylphenyl)boronic acid
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(4-(Benzyloxy)-2,6-dimethylphenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry for the construction of biaryl compounds, which are essential building blocks in the development of various drugs and bioactive molecules. The compound serves as a key intermediate, enabling the formation of carbon-carbon bonds between aryl groups, a critical step in synthesizing complex organic

(4-(Benzyloxy)-2,6-dimethylphenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry for the construction of biaryl compounds, which are essential building blocks in the development of various drugs and bioactive molecules. The compound serves as a key intermediate, enabling the formation of carbon-carbon bonds between aryl groups, a critical step in synthesizing complex organic molecules. Additionally, its boronic acid group makes it valuable in the preparation of sensors and probes for detecting specific analytes in biochemical research. Its application extends to materials science, where it contributes to the development of advanced polymers and organic electronic materials.

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