(3-((Phenylamino)methyl)phenyl)boronic acid

95%

Reagent Code: #226429
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CAS Number 690957-43-8

science Other reagents with same CAS 690957-43-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.07 g/mol
Formula C₁₃H₁₄BNO₂
badge Registry Numbers
MDL Number MFCD10699626
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Commonly applied in pharmaceutical research and development for synthesizing drug candidates and bioactive molecules. Also serves as a building block in materials science for developing fluorescent sensors and functional polymers. Its boronic acid group allows for reversible interactions with diols, making it useful in carbohydrate recognition and sensing applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿12,800.00
5g
10-20 days ฿38,400.00
(3-((Phenylamino)methyl)phenyl)boronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Commonly applied in pharmaceutical research and development for synthesizing drug candidates and bioactive molecules. Also serves as a building block in materials science for developing fluorescent sensors and functional polymers. Its boronic acid group allows for reversible interactions with diols, making it useful in carbohydrate recognitio

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Commonly applied in pharmaceutical research and development for synthesizing drug candidates and bioactive molecules. Also serves as a building block in materials science for developing fluorescent sensors and functional polymers. Its boronic acid group allows for reversible interactions with diols, making it useful in carbohydrate recognition and sensing applications.

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