N-methyliminodiethyl 4-formylbenzeneboronate

97%

Reagent Code: #218020
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CAS Number 128376-66-9

science Other reagents with same CAS 128376-66-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.071 g/mol
Formula C₁₂H₁₆BNO₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Its aldehyde and boronate functional groups allow sequential or selective transformations, making it valuable in constructing complex organic molecules, particularly in drug discovery and development. The N-methyliminodiethyl group enhances stability and handling compared to other boronate esters, improving shelf life and reaction reproducibility. Commonly employed in the preparation of biaryl compounds and functionalized aromatic systems found in bioactive molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿9,360.00
250mg
10-20 days ฿15,920.00
1g
10-20 days ฿47,920.00
N-methyliminodiethyl 4-formylbenzeneboronate
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Its aldehyde and boronate functional groups allow sequential or selective transformations, making it valuable in constructing complex organic molecules, particularly in drug discovery and development. The N-methyliminodiethyl group enhances stability and handling compared to other boronate esters, improving shelf life and reaction reproducibility. Commonly empl

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Its aldehyde and boronate functional groups allow sequential or selective transformations, making it valuable in constructing complex organic molecules, particularly in drug discovery and development. The N-methyliminodiethyl group enhances stability and handling compared to other boronate esters, improving shelf life and reaction reproducibility. Commonly employed in the preparation of biaryl compounds and functionalized aromatic systems found in bioactive molecules.

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