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Catalog Number:
40307
CAS Number:
374538-01-9
4-Fluoro-3-formylphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
4-Fluoro-3-formylbenzeneboronic acid
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Product Information

4-Fluoro-3-formylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its unique ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the development of complex organic molecules, including pharmaceuticals and agrochemicals. Its fluorine substituent enhances the electronic properties of the compound, allowing for improved reactivity and selectivity in various chemical transformations.

Researchers and industry professionals can leverage 4-Fluoro-3-formylphenylboronic acid in the synthesis of biologically active compounds, particularly in the creation of targeted therapies and novel materials. Its application in the preparation of fluorescent probes and sensors further highlights its significance in analytical chemistry. With its advantageous properties, this compound stands out as a valuable tool for advancing research and development in multiple fields, including drug discovery and materials science.

Synonyms
4-Fluoro-3-formylbenzeneboronic acid
CAS Number
374538-01-9
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H6BFO3
Molecular Weight
167.93
MDL Number
MFCD02093074
PubChem ID
2778651
Melting Point
220 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
4-Fluoro-3-formylbenzeneboronic acid
CAS Number
374538-01-9
Purity
95 - 105% (Assay by titration)
Molecular Formula
C7H6BFO3
Molecular Weight
167.93
MDL Number
MFCD02093074
PubChem ID
2778651
Melting Point
220 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Fluoro-3-formylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, allowing researchers to create complex molecules efficiently.
  • Drug Development: Its unique reactivity makes it valuable in the development of targeted therapies, particularly in oncology, where precision is crucial for effective treatment.
  • Materials Science: Used in the preparation of functionalized materials, it contributes to the development of advanced polymers and nanomaterials with enhanced properties.
  • Bioconjugation: This chemical facilitates the attachment of biomolecules in the creation of bioconjugates, which are essential for drug delivery systems and diagnostic applications.
  • Analytical Chemistry: It aids in the development of sensors and analytical methods, improving detection limits and specificity for various analytes in complex samples.

Citations