(3-Fluoro-2-formylphenyl)boronic acid

98%

Reagent Code: #90138
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CAS Number 871126-15-7

science Other reagents with same CAS 871126-15-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.93 g/mol
Formula C₇H₆BFO₃
thermostat Physical Properties
Melting Point 123-127°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting specific enzymes or receptors. It is also employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to create complex organic molecules for material science and medicinal chemistry. Additionally, it serves as a building block in the production of advanced materials, including polymers and sensors, due to its boronic acid group, which can interact with diols and sugars. Its applications extend to research in organic synthesis, where it aids in the creation of novel compounds with potential biological activity.

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Test Parameter Specification
Appearance White to Tan Solid
Purity 97.5-100
Melting Point 120-130

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿270.00
inventory 1g
10-20 days ฿350.00
inventory 5g
10-20 days ฿870.00
inventory 25g
10-20 days ฿3,010.00
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(3-Fluoro-2-formylphenyl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting specific enzymes or receptors. It is also employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to create complex organic molecules for material science and medicinal chemistry. Additionally, it serves as a building block in the production of advanced materials, including polymers and sensors, due to its boronic acid group, which can interact with diols and sugars. Its appli

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting specific enzymes or receptors. It is also employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to create complex organic molecules for material science and medicinal chemistry. Additionally, it serves as a building block in the production of advanced materials, including polymers and sensors, due to its boronic acid group, which can interact with diols and sugars. Its applications extend to research in organic synthesis, where it aids in the creation of novel compounds with potential biological activity.

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