Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
40290
CAS Number:
139911-29-8
4-Fluoro-2-methylphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-Fluoro-2-methylbenzeneboronic acid
Documents
$101.45 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

4-Fluoro-2-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 substitution enhances its reactivity and selectivity, allowing for the development of targeted therapies and advanced materials. Researchers appreciate its role in the creation of biologically active compounds, as it can facilitate the formation of carbon-carbon bonds with high efficiency.

In addition to its applications in synthetic chemistry, 4-Fluoro-2-methylphenylboronic acid is also employed in the development of sensors and diagnostic tools due to its ability to form stable complexes with various substrates. This compound's favorable properties, such as its solubility in organic solvents and compatibility with a range of reaction conditions, make it an ideal choice for both academic and industrial applications. By incorporating this compound into your research or production processes, you can enhance the efficiency and effectiveness of your chemical transformations.

Synonyms
4-Fluoro-2-methylbenzeneboronic acid
CAS Number
139911-29-8
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H8BFO2
Molecular Weight
153.95
MDL Number
MFCD02093072
PubChem ID
2734665
Melting Point
201 °C (Lit.)
Appearance
White to slightly yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Fluoro-2-methylbenzeneboronic acid
CAS Number
139911-29-8
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H8BFO2
Molecular Weight
153.95
MDL Number
MFCD02093072
PubChem ID
2734665
Melting Point
201 °C (Lit.)
Appearance
White to slightly yellow crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Pharmaceutical Development: This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents. Its unique properties allow for targeted drug design, enhancing efficacy.
  • Organic Synthesis: It is commonly used in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in organic chemistry. This application is vital for creating complex organic molecules in materials science and drug discovery.
  • Bioconjugation: The boronic acid group can selectively bind to diols, making it useful for bioconjugation processes. This is particularly beneficial in creating targeted delivery systems in biotechnology and medical research.
  • Sensor Technology: Its ability to form complexes with sugars makes it valuable in developing biosensors for glucose monitoring, which is crucial for diabetes management and research in medical diagnostics.
  • Material Science: The compound can be incorporated into polymer matrices to enhance properties such as thermal stability and mechanical strength, making it useful in the production of advanced materials for various industrial applications.

Citations