5-BROMO-2-TRIFLUOROMETHOXYPHENYLBORONIC ACID

98%

Reagent Code: #90902
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CAS Number 1072951-56-4

science Other reagents with same CAS 1072951-56-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.8230096 g/mol
Formula C₇H₅BBrF₃O₃
badge Registry Numbers
MDL Number MFCD11504857
thermostat Physical Properties
Boiling Point 326.8±52.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.79±0.1g/ml(Predicted)
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily used as a building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the pharmaceutical and agrochemical industries to create complex molecules by forming carbon-carbon bonds. Its boronic acid group facilitates the coupling with aryl or vinyl halides, enabling the synthesis of biaryl compounds, which are essential in drug development and material science. Additionally, it may be utilized in the preparation of intermediates for active pharmaceutical ingredients (APIs) or specialty chemicals. Its trifluoromethoxy group can enhance the stability and bioavailability of the resulting compounds, making it valuable in medicinal chemistry.

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Test Parameter Specification
Appearance White to off-white Solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,465.00
inventory 5g
10-20 days ฿7,389.00

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5-BROMO-2-TRIFLUOROMETHOXYPHENYLBORONIC ACID
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This compound is primarily used as a building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the pharmaceutical and agrochemical industries to create complex molecules by forming carbon-carbon bonds. Its boronic acid group facilitates the coupling with aryl or vinyl halides, enabling the synthesis of biaryl compounds, which are essential in drug development and material science. Additionally, it may be utilized in the preparation of intermediates for active pharmaceutical ingredients (APIs) or specialty chemicals. Its trifluoromethoxy group can enhance the stability and bioavailability of the resulting compounds, making it valuable in medicinal chemistry.
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