N-methyldiethanolamine phenylboronic ester

98%

Reagent Code: #218019
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CAS Number 65796-77-2

science Other reagents with same CAS 65796-77-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.076 g/mol
Formula C₁₁H₁₈BNO₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. Its boronic ester functionality allows for selective transformations in complex molecule assembly, including pharmaceuticals and agrochemicals. The presence of the N-methyldiethanolamine group enhances solubility and stability, making it suitable for aqueous reaction conditions. Also employed in sensor development for saccharide detection due to the reversible interaction between boronic acid derivatives and diols.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,280.00
inventory 5g
10-20 days ฿4,580.00
inventory 25g
10-20 days ฿16,480.00
N-methyldiethanolamine phenylboronic ester
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Used as a key reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. Its boronic ester functionality allows for selective transformations in complex molecule assembly, including pharmaceuticals and agrochemicals. The presence of the N-methyldiethanolamine group enhances solubility and stability, making it suitable for aqueous reaction conditions. Also employed in sensor development for saccharide detection due

Used as a key reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. Its boronic ester functionality allows for selective transformations in complex molecule assembly, including pharmaceuticals and agrochemicals. The presence of the N-methyldiethanolamine group enhances solubility and stability, making it suitable for aqueous reaction conditions. Also employed in sensor development for saccharide detection due to the reversible interaction between boronic acid derivatives and diols.

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