957120-53-5

Basic information

• Product Name: 3-Carbamoyl-5-chlorophenylboronic acid
• Synonyms: 3-Carbamoyl-5-chlorophenylboronic acid;3-Borono-5-chlorobenzamide, 3-(Aminocarbonyl)-5-chlorobenzeneboronic acid
• CAS NO: 957120-53-5
• Molecular Formula: C7H7BClNO3
• Molecular Weight: 199.4
• Product Categories: blocks;BoronicAcids;Carboxes
• Mol File: 957120-53-5.mol

Chemical Properties

• Boiling Point: 392.8±52.0 °C(Predicted)
• Appearance: /
• Density: 1.47±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 6.87±0.10(Predicted)
• CAS DataBase Reference: 3-Carbamoyl-5-chlorophenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Carbamoyl-5-chlorophenylboronic acid(957120-53-5)
• EPA Substance Registry System: 3-Carbamoyl-5-chlorophenylboronic acid(957120-53-5)

Safety Data

• Hazardous Substances Data: 957120-53-5(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
3-Carbamoyl-5-chlorophenylboronic acid is used as a building block in organic synthesis for the production of pharmaceuticals and agrochemicals. Its unique structure allows for the creation of complex organic molecules, making it a valuable component in the synthesis of various compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-Carbamoyl-5-chlorophenylboronic acid is utilized as a reagent for the development of new drugs. Its boronic acid functional group enables it to form stable bonds with other molecules, facilitating the synthesis of bioactive compounds with potential therapeutic applications.
Used in Material Science:
3-Carbamoyl-5-chlorophenylboronic acid has potential applications in the development of new materials due to its unique chemical properties. Its boronic acid functional group can be used to create novel materials with specific properties, such as improved thermal stability or enhanced catalytic activity.
Used in Catalyst Development:
The boronic acid functional group present in 3-Carbamoyl-5-chlorophenylboronic acid also makes it a promising candidate for the development of new catalysts. Its ability to form stable bonds with other molecules can be harnessed to create catalysts that improve the efficiency and selectivity of various chemical reactions.