3-Chloro-4-(N,N-diethylcarbamoyl)phenylboronic acid

≥95%

Reagent Code: #90201
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CAS Number 850589-48-9

science Other reagents with same CAS 850589-48-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.51 g/mol
Formula C₁₁H₁₅BClNO₃
badge Registry Numbers
MDL Number MFCD07363773
thermostat Physical Properties
Melting Point 148-152 °C
Boiling Point 466.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its stability and reactivity also make it suitable for use in research and development of new chemical entities.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,592.00

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3-Chloro-4-(N,N-diethylcarbamoyl)phenylboronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its stability and reactivity also make it suitable for use in research and development of new chemical entities.
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