3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

≥98%

Reagent Code: #90259
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CAS Number 380151-86-0

science Other reagents with same CAS 380151-86-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.09 g/mol
Formula C₁₃H₁₇BO₃
badge Registry Numbers
MDL Number MFCD05663872
thermostat Physical Properties
Melting Point 50-54°C
Boiling Point 345.1°C
inventory_2 Storage & Handling
Density 1.06g/cm3
Storage room temperature, 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 intermediate for constructing complex aromatic systems. Its boronate ester group allows for efficient coupling with aryl halides, enabling the formation of biaryl structures, which are essential in pharmaceuticals, agrochemicals, and materials science. Additionally, the aldehyde functional group provides a versatile handle for further chemical modifications, such as condensation or reduction reactions, making it valuable in the synthesis of fine chemicals and polymers. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.

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Test Parameter Specification
Appearance White Solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
Note Low melting point solid; may change state in different environments (solid, liquid, or semi-solid)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿320.00
inventory 1g
10-20 days ฿1,160.00
inventory 5g
10-20 days ฿2,980.00
inventory 25g
10-20 days ฿6,210.00

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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
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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 intermediate for constructing complex aromatic systems. Its boronate ester group allows for efficient coupling with aryl halides, enabling the formation of biaryl structures, which are essential in pharmaceuticals, agrochemicals, and materials science. Additionally, the aldehyde functional group provides a versatile handle for further chemical modifications, such as condensation or reduction reactions, making it valuable in the synthesis of fine chemicals and polymers. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.
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