Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
40103
CAS Number:
351422-73-6
3-Carbamoylphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
3-Carbamoylbenzeneboronic acid
Documents
$51.18 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

3-Carbamoylphenylboronic acid is a versatile compound recognized for its unique properties and applications in various fields, particularly in medicinal chemistry and materials science. This boronic acid derivative features a carbamoyl group, enhancing its reactivity and making it a valuable building block in the synthesis of biologically active molecules. Its ability to form reversible covalent bonds with diols and other nucleophiles positions it as a crucial component in drug discovery and development, particularly in the design of inhibitors for glycosidases and proteases.

In addition to its pharmaceutical applications, 3-Carbamoylphenylboronic acid is also utilized in the development of advanced materials, including sensors and catalysts. Its compatibility with various synthetic methodologies allows researchers to explore innovative pathways for creating complex structures. The compound's stability and ease of handling further enhance its appeal, making it an excellent choice for both academic research and industrial applications. With its broad range of uses, 3-Carbamoylphenylboronic acid stands out as a key player in the advancement of chemical research and development.

Synonyms
3-Carbamoylbenzeneboronic acid
CAS Number
351422-73-6
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H8BNO3
Molecular Weight
164.96
MDL Number
MFCD03411948
PubChem ID
2737814
Melting Point
226 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3-Carbamoylbenzeneboronic acid
CAS Number
351422-73-6
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H8BNO3
Molecular Weight
164.96
MDL Number
MFCD03411948
PubChem ID
2737814
Melting Point
226 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Carbamoylphenylboronic acid is widely utilized in research focused on:

  • Medicinal Chemistry: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing anti-cancer agents. Its ability to form stable complexes with biomolecules enhances drug efficacy.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems and diagnostics.
  • Organic Synthesis: Researchers leverage its boronic acid functionality in Suzuki-Miyaura cross-coupling reactions, which are essential for creating complex organic molecules in materials science and organic electronics.
  • Environmental Applications: The compound is explored for its potential in environmental chemistry, particularly in the detection and removal of pollutants, thanks to its ability to form complexes with various contaminants.
  • Research in Catalysis: It plays a role in catalytic processes, improving reaction efficiencies in organic synthesis, and offering advantages over traditional catalysts by providing more selective pathways.

Citations