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

97%

Reagent Code: #240746
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CAS Number 380151-85-9

science Other reagents with same CAS 380151-85-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.08 g/mol
Formula C₁₃H₁₇BO₃
thermostat Physical Properties
Boiling Point 345.9°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used primarily in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceuticals and agrochemicals. Its aldehyde and boronate functional groups allow sequential transformations, making it valuable in the preparation of complex aromatic and heteroaromatic systems. Commonly employed in the development of luminescent materials, sensors, and conjugated polymers for optoelectronic devices. Also utilized in medicinal chemistry for constructing biaryl aldehyde intermediates in drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿121.00
inventory 1g
10-20 days ฿137.50
inventory 5g
10-20 days ฿600.00
inventory 25g
10-20 days ฿2,860.00
inventory 100g
10-20 days ฿10,680.00
inventory 500g
10-20 days ฿48,120.00

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2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
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Used primarily in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceuticals and agrochemicals. Its aldehyde and boronate functional groups allow sequential transformations, making it valuable in the preparation of complex aromatic and heteroaromatic systems. Commonly employed in the development of luminescent materials, sensors, and conjugated polymers for optoelectronic devices. Also utilized in medicinal chemistry

Used primarily in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceuticals and agrochemicals. Its aldehyde and boronate functional groups allow sequential transformations, making it valuable in the preparation of complex aromatic and heteroaromatic systems. Commonly employed in the development of luminescent materials, sensors, and conjugated polymers for optoelectronic devices. Also utilized in medicinal chemistry for constructing biaryl aldehyde intermediates in drug discovery.

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