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Catalog Number:
40308
CAS Number:
850593-06-5
3-Fluoro-5-methylphenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
3-Fluoro-5-methylbenzeneboronic acid
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Product Information

3-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. Researchers and industry professionals leverage its unique properties to synthesize a variety of biologically active compounds, including pharmaceuticals and agrochemicals. Its fluorine substituent enhances the compound's electronic properties, providing improved reactivity and selectivity in chemical transformations.

In addition to its role in synthetic chemistry, 3-Fluoro-5-methylphenylboronic acid is also valuable in the development of sensors and materials due to its ability to interact with specific biomolecules. This compound's applications extend to the fields of drug discovery and development, where it aids in the creation of targeted therapies. With its favorable characteristics and broad applicability, 3-Fluoro-5-methylphenylboronic acid stands out as a crucial tool for researchers aiming to innovate in various chemical domains.

Synonyms
3-Fluoro-5-methylbenzeneboronic acid
CAS Number
850593-06-5
Purity
98 - 105% (Assay by titration)
Molecular Formula
C7H8BFO2
Molecular Weight
153.95
MDL Number
MFCD07363785
PubChem ID
19261265
Melting Point
222 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Fluoro-5-methylbenzeneboronic acid
CAS Number
850593-06-5
Purity
98 - 105% (Assay by titration)
Molecular Formula
C7H8BFO2
Molecular Weight
153.95
MDL Number
MFCD07363785
PubChem ID
19261265
Melting Point
222 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 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-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. Its unique structure allows for the creation of more effective therapeutic agents.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which are essential for forming carbon-carbon bonds in organic chemistry. This application is crucial for creating complex organic molecules used in various industries.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials, enhancing properties like conductivity and strength. This is particularly beneficial in electronics and packaging industries.
  • Bioconjugation: It plays a role in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules. This is important in the field of diagnostics and therapeutics, improving the efficacy of drug delivery systems.
  • Environmental Applications: The compound can be utilized in the detection and removal of pollutants, such as heavy metals, from water sources. Its ability to form stable complexes makes it valuable in environmental chemistry for developing remediation strategies.

Citations