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Catalog Number:
31066
CAS Number:
244205-40-1
2-Bromophenylboronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
o-Bromophenylboronic acid, 2-Bromobenzeneboronic acid
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Product Information

2-Bromophenylboronic 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 Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals leverage its unique properties to create complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals. Its reactivity and selectivity allow for the efficient construction of carbon-carbon bonds, facilitating the synthesis of biologically active compounds.

Additionally, 2-Bromophenylboronic acid serves as a valuable building block in the preparation of various functionalized materials, including polymers and sensors. Its applications extend to the field of materials science, where it contributes to the development of advanced materials with tailored properties. With its proven effectiveness and broad applicability, this compound stands out as a key player in both research and industrial settings, offering significant advantages over similar compounds in terms of reactivity and ease of use.

Synonyms
o-Bromophenylboronic acid, 2-Bromobenzeneboronic acid
CAS Number
244205-40-1
Purity
≥ 99% (HPLC)
Molecular Formula
C6H6BBrO2
Molecular Weight
200.83
MDL Number
MFCD01114672
PubChem ID
2773294
Melting Point
113 - 115 ?C
Appearance
White to off-white powder
Conditions
Store at 2-8 °C
General Information
Synonyms
o-Bromophenylboronic acid, 2-Bromobenzeneboronic acid
CAS Number
244205-40-1
Purity
≥ 99% (HPLC)
Molecular Formula
C6H6BBrO2
Molecular Weight
200.83
MDL Number
MFCD01114672
PubChem ID
2773294
Melting Point
113 - 115 ?C
Appearance
White to off-white 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

2-Bromophenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound is a valuable building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura coupling reactions, allowing researchers to create complex carbon-carbon bonds, which are essential in material science and medicinal chemistry.
  • Bioconjugation: The ability to form stable bonds with biomolecules makes it useful in bioconjugation processes, enhancing the development of targeted drug delivery systems.
  • Fluorescent Probes: Its unique properties enable the design of fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes in real-time.
  • Sensor Development: This compound is utilized in the creation of sensors for detecting various analytes, offering advantages in environmental monitoring and safety applications.

Citations