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Catalog Number:
40128
CAS Number:
51323-43-4
Ácido 3-(bromometil)fenilborónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 3-(bromometil)bencenoborónico
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$52.68 /1G
Tamaño
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Product Information

3-(Bromomethyl)phenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules. Its unique bromomethyl group enhances its reactivity, allowing for the formation of carbon-carbon bonds that are crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Researchers appreciate its role in the creation of biologically active compounds, as it can facilitate the introduction of various functional groups into aromatic systems.

In addition to its synthetic applications, 3-(Bromomethyl)phenylboronic acid is also employed in the development of sensors and in the field of materials science, where it contributes to the design of novel polymers and nanomaterials. Its compatibility with various reaction conditions and ease of handling make it a preferred choice for chemists seeking reliable and efficient methods for compound synthesis. With its broad range of applications, this compound stands out as a valuable asset in both research and industrial settings.

Synonyms
Ácido 3-(bromometil)bencenoborónico
CAS Number
51323-43-4
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C7H8BBrO2
Molecular Weight
214.85
MDL Number
MFCD01632207
PubChem ID
2773281
Melting Point
216 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Ácido 3-(bromometil)bencenoborónico
CAS Number
51323-43-4
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C7H8BBrO2
Molecular Weight
214.85
MDL Number
MFCD01632207
PubChem ID
2773281
Melting Point
216 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-(Bromomethyl)phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, allowing researchers to create complex biaryl structures that are essential in drug development.
  • Material Science: This chemical plays a role in the modification of polymers, enhancing their properties for applications in electronics and coatings.
  • Bioconjugation: The boronic acid group can selectively bind to diols, making it useful in bioconjugation techniques for labeling biomolecules in research and diagnostics.
  • Fluorescent Probes: It is also used in the development of fluorescent probes for detecting biological molecules, providing valuable tools for researchers in the field of biochemistry.

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