trans-3-Phenyl-1-propen-1-ylboronic acid

95%

Reagent Code: #122336
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CAS Number 129423-29-6

science Other reagents with same CAS 129423-29-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.99 g/mol
Formula C₉H₁₁BO₂
badge Registry Numbers
MDL Number MFCD06202527
thermostat Physical Properties
Boiling Point 329.2±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.084±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, enabling the construction of complex organic molecules. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of bioactive compounds and fine chemicals, where precise molecular structures are essential. Its stability and reactivity under mild conditions make it a versatile tool in modern synthetic chemistry.

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Test Parameter Specification
APPEARANCE White to Faint Beige Powder or Crystals or Chunk(s) or Powder with Chunk(s) or Crystals with Chunk(s)
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿18,160.00

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trans-3-Phenyl-1-propen-1-ylboronic acid
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, enabling the construction of complex organic molecules. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of bioactive compounds and fine chemicals, where precise molecular structures are essential. Its stability and reactivity under mild conditions make it a versatile tool in modern synthetic chemistry.
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