4-((N,N-Dimethylamino)methyl)phenylboronic acid pinacol ester HCl

95%

Reagent Code: #218733
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CAS Number 1073371-85-3

science Other reagents with same CAS 1073371-85-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.63 g/mol
Formula C₁₅H₂₅BClNO₂
badge Registry Numbers
MDL Number MFCD07771993
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions as a boronic ester reagent for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. The dimethylaminomethyl group enhances solubility and can act as a directing or coordinating group in metal-catalyzed reactions. Commonly employed in the development of complex organic molecules, including drug candidates, due to its stability and reactivity profile. Also utilized in probe and sensor design where controlled boronate reactivity is required.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,090.00
inventory 5g
10-20 days ฿17,570.00
inventory 25g
10-20 days ฿61,510.00
4-((N,N-Dimethylamino)methyl)phenylboronic acid pinacol ester HCl
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Used in Suzuki-Miyaura cross-coupling reactions as a boronic ester reagent for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. The dimethylaminomethyl group enhances solubility and can act as a directing or coordinating group in metal-catalyzed reactions. Commonly employed in the development of complex organic molecules, including drug candidates, due to its stability and reactivity profile. Also utilized in probe and sensor design where controlled boronate reactivity is re

Used in Suzuki-Miyaura cross-coupling reactions as a boronic ester reagent for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. The dimethylaminomethyl group enhances solubility and can act as a directing or coordinating group in metal-catalyzed reactions. Commonly employed in the development of complex organic molecules, including drug candidates, due to its stability and reactivity profile. Also utilized in probe and sensor design where controlled boronate reactivity is required.

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