4-(N,N-Dimethylaminosulfonyl)phenylboronic acid pinacol ester

95%

Reagent Code: #90502
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CAS Number 486422-04-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.21 g/mol
Formula C₁₄H₂₂BNO₄S
badge Registry Numbers
MDL Number MFCD03425962
thermostat Physical Properties
Boiling Point 415.2±47.0 °C (Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic ester group makes it a valuable reagent for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. It is also employed in the preparation of biaryl compounds, which are essential in material science and drug development. Additionally, its sulfonamide group enhances solubility and stability, making it suitable for use in aqueous or mixed-solvent systems. This compound is particularly useful in the development of fluorescent probes and sensors due to its ability to interact with specific analytes or biomolecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days €188.43
inventory 5g
10-20 days €565.53
4-(N,N-Dimethylaminosulfonyl)phenylboronic acid pinacol ester
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic ester group makes it a valuable reagent for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. It is also employed in the preparation of biaryl compounds, which are essential in material science and drug development. Additionally, its sulfonamide group enhances solubility and stability, making it suitable for use in aqueous or mixed-solvent systems. This compound is particularly useful in the development of fluorescent probes and sensors due to its ability to interact with specific analytes or biomolecules.
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