4-CHLORO-3-(N,N-DIETHYLCARBAMOYL)PHENYLBORONIC ACID

98%

Reagent Code: #90627
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CAS Number 871332-68-2

science Other reagents with same CAS 871332-68-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.51 g/mol
Formula C₁₁H₁₅BClNO₃
badge Registry Numbers
MDL Number MFCD07363797
thermostat Physical Properties
Melting Point 130-134 °C
Boiling Point 467.5±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.25±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in constructing complex organic molecules. Additionally, it serves as a building block in the development of bioactive compounds and drug candidates, contributing to research in medicinal chemistry. Its stability and reactivity also make it suitable for use in material science, particularly in the creation of polymers and electronic materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,645.00
inventory 1g
10-20 days ฿10,224.00

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4-CHLORO-3-(N,N-DIETHYLCARBAMOYL)PHENYLBORONIC ACID
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Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in constructing complex organic molecules. Additionally, it serves as a building block in the development of bioactive compounds and drug candidates, contributing to research in medicinal chemistry. It

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in constructing complex organic molecules. Additionally, it serves as a building block in the development of bioactive compounds and drug candidates, contributing to research in medicinal chemistry. Its stability and reactivity also make it suitable for use in material science, particularly in the creation of polymers and electronic materials.

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