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

Catalog Number:
40264
CAS Number:
151169-74-3
2,3-Dichlorophenylboronic acid
Purity:
≥ 97% (NMR)
Synonym(s):
2,3-Dichlorobenzeneboronic acid
Documents
$75.11 /5G
Pack Size Availability Price
Request Bulk Quote
Product Information

2,3-Dichlorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceutical agents and agrochemicals. Its unique structure allows for selective functionalization, which is particularly beneficial in the synthesis of complex molecules. Researchers have leveraged 2,3-Dichlorophenylboronic acid in cross-coupling reactions, such as Suzuki-Miyaura coupling, to create carbon-carbon bonds, thereby facilitating the construction of intricate organic frameworks.

In addition to its synthetic applications, 2,3-Dichlorophenylboronic acid has shown promise in the field of sensor technology, particularly in the detection of glucose and other biomolecules. Its ability to interact with specific biological targets positions it as a valuable tool in the development of diagnostic devices. With its robust reactivity and functional versatility, 2,3-Dichlorophenylboronic acid stands out as a critical compound for researchers and industry professionals seeking innovative solutions in chemical synthesis and analytical applications.

Synonyms
2,3-Dichlorobenzeneboronic acid
CAS Number
151169-74-3
Purity
≥ 97% (NMR)
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.81
MDL Number
MFCD01075703
PubChem ID
2734661
Melting Point
248 - 250 °C
Appearance
White solid
Conditions
Store at RT
General Information
Synonyms
2,3-Dichlorobenzeneboronic acid
CAS Number
151169-74-3
Purity
≥ 97% (NMR)
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.81
MDL Number
MFCD01075703
PubChem ID
2734661
Melting Point
248 - 250 °C
Appearance
White solid
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,3-Dichlorophenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals, enhancing efficiency in creating complex structures.
  • Medicinal Chemistry: It plays a significant role in drug discovery, especially in the design of inhibitors for certain enzymes, which can lead to the development of new therapeutic agents for diseases such as cancer.
  • Material Science: Used in the preparation of boron-containing polymers, it contributes to the development of advanced materials with improved properties, such as enhanced thermal stability and mechanical strength.
  • Bioconjugation: The compound is effective in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial for creating targeted drug delivery systems.
  • Analytical Chemistry: It is utilized in the development of sensors and analytical methods for detecting specific biomolecules, providing a reliable approach for monitoring various biological processes.

Citations