(E)-4-(2-Carboxyvinyl)phenylboronic Acid Pinacol Ester

≥95%

Reagent Code: #89401
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CAS Number 1072944-97-8

science Other reagents with same CAS 1072944-97-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.12 g/mol
Formula C₁₅H₁₉O₄B
badge Registry Numbers
MDL Number MFCD11053843
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical industry, where it aids in the development of drug candidates. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many active pharmaceutical ingredients. Additionally, it is employed in material science for the synthesis of conjugated polymers and organic electronic materials, contributing to advancements in organic light-emitting diodes (OLEDs) and other optoelectronic devices. Its stability and reactivity make it a valuable tool in modern synthetic chemistry.

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Test Parameter Specification
Appearance White Crystalline Powder
Purity 95-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,800.00
inventory 5g
10-20 days ฿39,100.00

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(E)-4-(2-Carboxyvinyl)phenylboronic Acid Pinacol Ester
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical industry, where it aids in the development of drug candidates. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many active pharmaceutical ingredients. Additionally, it is employed in material scien
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical industry, where it aids in the development of drug candidates. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many active pharmaceutical ingredients. Additionally, it is employed in material science for the synthesis of conjugated polymers and organic electronic materials, contributing to advancements in organic light-emitting diodes (OLEDs) and other optoelectronic devices. Its stability and reactivity make it a valuable tool in modern synthetic chemistry.
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