871332-68-2

Basic information

• Product Name: 4-CHLORO-3-(N,N-DIETHYLCARBAMOYL)PHENYLBORONIC ACID
• Synonyms: 4-CHLORO-3-(N,N-DIETHYLCARBAMOYL)PHENYLBORONIC ACID;N,N-DIETHYL 2-CHLORO-5-BORONOBENZAMIDE;N,N-Diethyl 5-borono-2-chlorobenzamide;4-Chloro-3-(diethylcarbaMoyl)benzeneboronic acid, 98%;(4-Chloro-3-(diethylcarbamoyl)phenyl)boronic acid
• CAS NO: 871332-68-2
• Molecular Formula: C11H15BClNO3
• Molecular Weight: 255.51
• Product Categories: blocks;BoronicAcids;Carboxes
• Mol File: 871332-68-2.mol

Chemical Properties

• Melting Point: 130-134℃
• Boiling Point: 467.5±55.0 °C(Predicted)
• Appearance: /
• Density: 1.25±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 7.77±0.10(Predicted)
• CAS DataBase Reference: 4-CHLORO-3-(N,N-DIETHYLCARBAMOYL)PHENYLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CHLORO-3-(N,N-DIETHYLCARBAMOYL)PHENYLBORONIC ACID(871332-68-2)
• EPA Substance Registry System: 4-CHLORO-3-(N,N-DIETHYLCARBAMOYL)PHENYLBORONIC ACID(871332-68-2)

Safety Data

• Hazardous Substances Data: 871332-68-2(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
4-CHLORO-3-(N,N-DIETHYLCARBAMOYL)PHENYLBORONIC ACID is used as a reagent in coupling reactions for the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals. Its diethylcarbamoyl group facilitates these reactions, making it a valuable component in the creation of new compounds with therapeutic or pesticidal properties.
Used in Organic Synthesis:
In the field of organic synthesis, 4-CHLORO-3-(N,N-DIETHYLCARBAMOYL)PHENYLBORONIC ACID is used as a precursor for the formation of carbon-carbon bonds through the Suzuki-Miyaura cross-coupling reaction. This reaction is a powerful tool for constructing new carbon frameworks, which are essential in the synthesis of a wide range of organic compounds.
Used in Antibacterial and Antifungal Applications:
4-CHLORO-3-(N,N-DIETHYLCARBAMOYL)PHENYLBORONIC ACID has been studied for its potential as an antibacterial and antifungal agent. Its ability to inhibit the growth of bacteria and fungi makes it a candidate for use in the development of new antimicrobial agents to combat drug-resistant infections.
Used in Research and Development:
In academic and industrial research settings, 4-CHLORO-3-(N,N-DIETHYLCARBAMOYL)PHENYLBORONIC ACID is utilized to explore new chemical reactions and pathways, as well as to investigate its potential applications in material science, medicinal chemistry, and other related fields. Its unique structure and reactivity make it an interesting subject for scientific inquiry and innovation.