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Catalog Number:
40330
CAS Number:
406482-20-0
2,6-Difluoro-4-methoxyphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
2,6-Difluoro-4-methoxybenzeneboronic acid
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Product Information

2,6-Difluoro-4-methoxyphenylboronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to form stable complexes with various substrates, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique fluorine and methoxy substituents enhance its reactivity and selectivity, allowing for the efficient synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Researchers have utilized this compound in the development of targeted therapies, particularly in oncology, where it aids in the design of potent inhibitors.

Additionally, 2,6-Difluoro-4-methoxyphenylboronic acid is valued for its compatibility with a range of functional groups, providing flexibility in synthetic pathways. Its application extends to the field of materials science, where it contributes to the development of advanced materials with tailored properties. The compound's stability and ease of handling make it a preferred choice for both academic and industrial laboratories, ensuring reliable results in various applications.

Synonyms
2,6-Difluoro-4-methoxybenzeneboronic acid
CAS Number
406482-20-0
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H7BF2O3
Molecular Weight
187.94
MDL Number
MFCD05664299
PubChem ID
16217424
Melting Point
130 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2,6-Difluoro-4-methoxybenzeneboronic acid
CAS Number
406482-20-0
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H7BF2O3
Molecular Weight
187.94
MDL Number
MFCD05664299
PubChem ID
16217424
Melting Point
130 °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

2,6-Difluoro-4-methoxyphenylboronic 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 anti-cancer agents, enhancing the efficiency of drug discovery processes.
  • Organic Synthesis: It is employed in Suzuki coupling reactions, which are vital for forming carbon-carbon bonds, making it essential for creating complex organic molecules in the chemical industry.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and nanomaterials, due to its unique electronic properties, which can improve material performance.
  • Bioconjugation: It plays a significant role in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other compounds, which is crucial in diagnostics and therapeutic applications.
  • Environmental Chemistry: This chemical can be utilized in the development of sensors for detecting environmental pollutants, providing a practical solution for monitoring and improving environmental health.

Citations