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Catalog Number:
40332
CAS Number:
212837-49-5
2,3-Difluoro-4-propoxyphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
2,3-Difluoro-4-propoxybenzeneboronic acid
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Product Information

2,3-Difluoro-4-propoxyphenylboronic acid is a versatile boronic acid derivative that plays a significant role in organic synthesis and medicinal chemistry. This compound is recognized for its unique ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its difluoro substituents enhance its reactivity and selectivity, allowing for more efficient coupling reactions in the synthesis of complex organic molecules. Researchers have utilized this compound in the development of targeted therapies and in the design of novel materials, particularly in the field of organic electronics.

The practical applications of 2,3-Difluoro-4-propoxyphenylboronic acid extend to its use in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in constructing carbon-carbon bonds. This compound's ability to facilitate the formation of diverse molecular architectures makes it invaluable for chemists seeking to innovate in drug discovery and materials science. Its stability and reactivity profile provide significant advantages over similar compounds, making it a preferred choice for professionals aiming to enhance the efficiency and effectiveness of their synthetic pathways.

Synonyms
2,3-Difluoro-4-propoxybenzeneboronic acid
CAS Number
212837-49-5
Purity
97 - 105% (Assay by titration)
Molecular Formula
C9H11BF2O3
Molecular Weight
215.99
MDL Number
MFCD14584457
PubChem ID
50878572
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2,3-Difluoro-4-propoxybenzeneboronic acid
CAS Number
212837-49-5
Purity
97 - 105% (Assay by titration)
Molecular Formula
C9H11BF2O3
Molecular Weight
215.99
MDL Number
MFCD14584457
PubChem ID
50878572
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

2,3-Difluoro-4-propoxyphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound plays a crucial role in the synthesis of boronic acid derivatives, which are essential in developing new drugs, particularly for cancer treatment.
  • Organic Synthesis: It is used as a key building block in organic chemistry, enabling the formation of complex molecules through Suzuki coupling reactions, which are vital in creating pharmaceuticals and agrochemicals.
  • Material Science: The compound is applied in the development of advanced materials, such as polymers and coatings, enhancing their properties like durability and resistance to environmental factors.
  • Bioconjugation: It serves as a tool in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is important in diagnostics and therapeutic applications.
  • Sensor Technology: This chemical is utilized in the fabrication of sensors, particularly for detecting biomolecules, providing a sensitive and selective method for monitoring biological processes.

Citations