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Catalog Number:
40244
CAS Number:
957121-05-0
3-Cyano-2-fluorophenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
3-Cyano-2-fluorobenzeneboronic acid, (3-Cyano-2-fluorophenyl)boronic acid
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Product Information

3-Cyano-2-fluorophenylboronic acid is a versatile compound widely utilized in pharmaceutical and chemical research. This boronic acid derivative is recognized for its unique ability to form reversible covalent bonds with diols, making it an essential reagent in the development of various organic compounds. Its application in Suzuki-Miyaura cross-coupling reactions allows for the synthesis of complex molecules, which are crucial in drug discovery and development. Additionally, its fluorine atom enhances the compound's electronic properties, making it particularly valuable in medicinal chemistry for designing potent bioactive molecules.

Researchers appreciate 3-Cyano-2-fluorophenylboronic acid for its stability and ease of use in various synthetic pathways. Its role in the preparation of targeted compounds for cancer therapy and other therapeutic areas highlights its significance in modern medicinal chemistry. With its unique properties and practical applications, this compound stands out as a key player in advancing chemical research and pharmaceutical innovation.

Synonyms
3-Cyano-2-fluorobenzeneboronic acid, (3-Cyano-2-fluorophenyl)boronic acid
CAS Number
957121-05-0
Purity
98 - 105% (Assay by titration)
Molecular Formula
C7H5BFNO2
Molecular Weight
164.93
MDL Number
MFCD07374984
PubChem ID
44558173
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Cyano-2-fluorobenzeneboronic acid, (3-Cyano-2-fluorophenyl)boronic acid
CAS Number
957121-05-0
Purity
98 - 105% (Assay by titration)
Molecular Formula
C7H5BFNO2
Molecular Weight
164.93
MDL Number
MFCD07374984
PubChem ID
44558173
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-Cyano-2-fluorophenylboronic 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 modification of bioactive molecules.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to create complex organic compounds. This application is vital in the production of agrochemicals and fine chemicals.
  • Material Science: The compound is used in the development of new materials, including polymers and nanomaterials, which have applications in electronics and coatings, enhancing their properties and performance.
  • Bioconjugation: Its boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation processes for labeling biomolecules in research and diagnostics.
  • Fluorescent Probes: The fluorine atom in its structure can be utilized to develop fluorescent probes for imaging applications in biological research, aiding in the visualization of cellular processes.

Citations