(4-(Decyloxy)phenyl)boronic acid

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Reagent Code: #113264
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CAS Number 147222-99-9

science Other reagents with same CAS 147222-99-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.20 g/mol
Formula C₁₆H₂₇BO₃
badge Registry Numbers
MDL Number MFCD01114674
thermostat Physical Properties
Boiling Point 421.5±47.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

(4-(Decyloxy)phenyl)boronic acid is primarily utilized in organic synthesis and material science due to its boronic acid functional group. It serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and polymers. Its decyloxy chain enhances solubility in organic solvents, making it suitable for applications in hydrophobic environments. Additionally, it is employed in the development of sensors and diagnostic tools, as boronic acids can selectively bind to diols and sugars, facilitating glucose detection in medical devices. The compound is also explored in the creation of self-assembled monolayers and advanced materials for surface modification.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,421.00
inventory 100mg
10-20 days ฿1,431.00

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(4-(Decyloxy)phenyl)boronic acid
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(4-(Decyloxy)phenyl)boronic acid is primarily utilized in organic synthesis and material science due to its boronic acid functional group. It serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and polymers. Its decyloxy chain enhances solubility in organic solvents, making it suitable for applications in hydrophobic environments. Additionally, it is employed in the

(4-(Decyloxy)phenyl)boronic acid is primarily utilized in organic synthesis and material science due to its boronic acid functional group. It serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and polymers. Its decyloxy chain enhances solubility in organic solvents, making it suitable for applications in hydrophobic environments. Additionally, it is employed in the development of sensors and diagnostic tools, as boronic acids can selectively bind to diols and sugars, facilitating glucose detection in medical devices. The compound is also explored in the creation of self-assembled monolayers and advanced materials for surface modification.

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