4-(4-Methylphenoxy) phenylboronic acid

95%

Reagent Code: #46330
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CAS Number 1311182-76-9

science Other reagents with same CAS 1311182-76-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.0781 g/mol
Formula C₁₄H₁₅BO₃
thermostat Physical Properties
Boiling Point 430.8±47.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3
Storage room temperature

description Product Description

Used as a key intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the creation of complex molecules for drug development. Additionally, it is utilized in the preparation of sensors and materials for detecting and binding specific biological molecules, making it valuable in diagnostic and analytical applications. Its boronic acid group enables it to interact with diols and sugars, contributing to its use in glucose sensing and carbohydrate chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,792.00
inventory 5g
10-20 days ฿65,592.00
inventory 1g
10-20 days ฿18,792.00

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4-(4-Methylphenoxy) phenylboronic acid
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Used as a key intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the creation of complex molecules for drug development. Additionally, it is utilized in the preparation of sensors and materials for detecting and binding specific biological molecules, making it valuable in diagnostic and analytical applications. Its boronic acid

Used as a key intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the creation of complex molecules for drug development. Additionally, it is utilized in the preparation of sensors and materials for detecting and binding specific biological molecules, making it valuable in diagnostic and analytical applications. Its boronic acid group enables it to interact with diols and sugars, contributing to its use in glucose sensing and carbohydrate chemistry.

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