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Catalog Number:
40219
CAS Number:
166328-16-1
Acide 2-fluoro-5-méthylphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 2-fluoro-5-méthylbenzèneboronique, Acide 6-fluoro- m -tolylboronique
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Product Information

2-Fluoro-5-methylphenylboronic 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. Its unique fluorine substitution enhances its reactivity and selectivity, allowing for the efficient synthesis of various biaryl compounds, which are crucial in the development of pharmaceuticals and agrochemicals. Researchers appreciate its role in the preparation of complex molecular architectures, particularly in the synthesis of biologically active molecules.

In addition to its synthetic applications, 2-Fluoro-5-methylphenylboronic acid serves as a valuable tool in the field of materials science, where it can be employed in the development of novel polymers and functional materials. Its compatibility with a range of substrates and its ability to facilitate the formation of carbon-carbon bonds make it a preferred choice for chemists aiming to innovate in drug discovery and materials engineering. This compound not only streamlines synthetic pathways but also enhances the efficiency of chemical processes, making it a significant asset in both research and industrial applications.

Synonyms
Acide 2-fluoro-5-méthylbenzèneboronique, Acide 6-fluoro- m -tolylboronique
CAS Number
166328-16-1
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 7 H 8 BFO 2
Molecular Weight
153.95
MDL Number
MFCD03428512
PubChem ID
10351884
Melting Point
77 - 82 °C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide 2-fluoro-5-méthylbenzèneboronique, Acide 6-fluoro- m -tolylboronique
CAS Number
166328-16-1
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 7 H 8 BFO 2
Molecular Weight
153.95
MDL Number
MFCD03428512
PubChem ID
10351884
Melting Point
77 - 82 °C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-Fluoro-5-methylphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and other diseases due to its ability to form stable complexes with biomolecules.
  • Material Science: It is used in the creation of advanced materials, including polymers and nanomaterials, which benefit from its unique boronic acid functionality, enhancing properties such as conductivity and mechanical strength.
  • Organic Synthesis: This chemical is a valuable reagent in cross-coupling reactions, allowing chemists to efficiently build complex organic molecules, which is essential in both academic and industrial settings.
  • Diagnostics: Its application extends to the development of diagnostic tools, where it aids in the detection of specific biomolecules, enhancing the sensitivity and specificity of tests.
  • Environmental Chemistry: The compound is also explored for its potential in environmental applications, such as the removal of pollutants from water, leveraging its ability to bind with various contaminants.

Citations