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Catalog Number:
28125
CAS Number:
10365-98-7
3-Methoxyphenylboronic acid
Synonym(s):
3-Boronanisole, Anisole-3-boronic acid
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Product Information

3-Methoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a methoxy group that enhances its reactivity and solubility, making it an excellent candidate for Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Its unique properties allow for the development of complex organic molecules, including pharmaceuticals and agrochemicals. Researchers appreciate its role in the synthesis of biologically active compounds, particularly in the creation of targeted therapies for various diseases.

In addition to its applications in synthetic organic chemistry, 3-Methoxyphenylboronic acid serves as a valuable tool in the development of sensors and materials science. Its ability to form stable complexes with diols makes it useful in the design of selective sensors for glucose and other biomolecules. The compound's favorable characteristics, such as high stability and ease of handling, further enhance its appeal for both academic and industrial applications. Whether in drug discovery or sensor technology, 3-Methoxyphenylboronic acid stands out as a key reagent that supports innovation and efficiency in research and development.

Synonyms
3-Boronanisole, Anisole-3-boronic acid
CAS Number
10365-98-7
Molecular Formula
C7H9BO3
Molecular Weight
151.96
MDL Number
MFCD00161359
PubChem ID
2734370
Conditions
Store at 0-8°C
General Information
Synonyms
3-Boronanisole, Anisole-3-boronic acid
CAS Number
10365-98-7
Molecular Formula
C7H9BO3
Molecular Weight
151.96
MDL Number
MFCD00161359
PubChem ID
2734370
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

3-Methoxyphenylboronic 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. Its ability to form stable complexes with other compounds enhances reaction efficiency.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura coupling reactions, which are essential for creating carbon-carbon bonds. This application is particularly valuable in the production of complex organic compounds used in drug discovery.
  • Fluorescent Probes: The compound is used in the design of fluorescent probes for biological imaging. Its unique properties allow for the visualization of cellular processes, aiding researchers in studying disease mechanisms.
  • Sensor Development: 3-Methoxyphenylboronic acid is employed in the development of chemical sensors for detecting glucose levels. This application is particularly beneficial in the medical field for diabetes management.
  • Material Science: It is utilized in the creation of advanced materials, such as polymers and nanomaterials, which have applications in electronics and energy storage, providing enhanced performance compared to traditional materials.

Citations