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Catalog Number:
40208
CAS Number:
168267-99-0
Ácido 3-fluoro-4-metilfenilborónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 3-fluoro-4-metilbencenoborónico, Ácido 3-fluoro- p -tolilborónico
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$39.56 /1G
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Product Information

3-Fluoro-4-methylphenylboronic 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, including pharmaceuticals and agrochemicals. Its unique fluorine substituent enhances the electronic properties of the molecule, allowing for improved reactivity and selectivity in various chemical transformations.

Researchers and industry professionals appreciate 3-Fluoro-4-methylphenylboronic acid for its role in developing targeted therapies and advanced materials. Its applications extend to the synthesis of biologically active compounds, where it can be used to modify drug candidates for enhanced efficacy and reduced side effects. Additionally, this compound's stability and compatibility with various reaction conditions make it a reliable choice for both laboratory and industrial applications, streamlining the synthesis process and improving overall yields.

Synonyms
Ácido 3-fluoro-4-metilbencenoborónico, Ácido 3-fluoro- p -tolilborónico
CAS Number
168267-99-0
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C7H8BFO2
Molecular Weight
153.95
MDL Number
MFCD02683115
PubChem ID
2782674
Melting Point
237 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 3-fluoro-4-metilbencenoborónico, Ácido 3-fluoro- p -tolilborónico
CAS Number
168267-99-0
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C7H8BFO2
Molecular Weight
153.95
MDL Number
MFCD02683115
PubChem ID
2782674
Melting Point
237 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Fluoro-4-methylphenylboronic 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 unique properties allow for selective reactions that can enhance yield and purity.
  • Drug Development: In medicinal chemistry, it plays a crucial role in the design of new drugs, especially those targeting specific biological pathways. Its ability to form stable complexes with biomolecules makes it valuable in creating targeted therapies.
  • Catalysis: It is used as a catalyst in cross-coupling reactions, which are essential in forming carbon-carbon bonds. This application is particularly beneficial in the production of complex organic compounds, streamlining processes in chemical manufacturing.
  • Material Science: The compound is applied in the development of advanced materials, including polymers and nanomaterials. Its boronic acid functionality allows for the formation of dynamic covalent bonds, leading to innovative material properties.
  • Analytical Chemistry: It is employed in various analytical techniques, such as chromatography and spectroscopy, to enhance the detection and quantification of specific analytes. This application is crucial for quality control in pharmaceuticals and environmental monitoring.

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