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Catalog Number:
26800
CAS Number:
5467-74-3
4-Bromophenylboronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
(4-Bromophenyl)boranediol
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Product Information

4-Bromophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique properties enable it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules. Researchers and industry professionals appreciate its role in the preparation of biologically active compounds, including those used in cancer research and drug development.

In addition to its synthetic applications, 4-Bromophenylboronic acid serves as a key building block in the production of sensors and materials for advanced technologies. Its reactivity with sugars and other biomolecules opens avenues for the development of innovative diagnostic tools. The compound's stability and ease of handling further enhance its appeal, making it a preferred choice for laboratories and industrial applications alike. With its broad range of uses, 4-Bromophenylboronic acid stands out as a valuable asset for researchers aiming to push the boundaries of chemical synthesis and material science.

Synonyms
(4-Bromophenyl)boranediol
CAS Number
5467-74-3
Purity
≥ 99% (HPLC)
Molecular Formula
C6H6BBrO2
Molecular Weight
200.83
MDL Number
MFCD00002104
PubChem ID
79599
Appearance
White to off-white powder
Conditions
Store at 0-8 °C
General Information
Synonyms
(4-Bromophenyl)boranediol
CAS Number
5467-74-3
Purity
≥ 99% (HPLC)
Molecular Formula
C6H6BBrO2
Molecular Weight
200.83
MDL Number
MFCD00002104
PubChem ID
79599
Appearance
White to off-white powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Organic Synthesis: This compound serves as a crucial building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is extensively used in Suzuki-Miyaura coupling reactions, allowing chemists to create complex biaryl compounds efficiently, which are important in medicinal chemistry.
  • Fluorescent Probes: Researchers employ it to develop fluorescent probes for biological imaging, enhancing the ability to visualize cellular processes in real-time.
  • Drug Development: The compound plays a significant role in the design of targeted therapies, particularly in cancer treatment, by facilitating the development of boron-containing drugs.
  • Material Science: It is utilized in the creation of advanced materials, including polymers and nanomaterials, which can be applied in electronics and sensors.

Citations