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Catalog Number:
31438
CAS Number:
352303-67-4
Acide 2-fluoro-3-méthoxyphénylboronique
Purity:
≥ 99,5 % (HPLC)
Synonym(s):
Acide 2-fluoro-3-méthoxybenzèneboronique
Documents
$22.03 /5G
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Product Information

Conserver à l'écart des substances incompatibles, des sources d'inflammation et des agents oxydants. Éviter les périodes de stockage prolongées.

Synonyms
Acide 2-fluoro-3-méthoxybenzèneboronique
CAS Number
352303-67-4
Purity
≥ 99,5 % (HPLC)
Molecular Formula
C 7 H 8 BFO 3
Molecular Weight
169.95
MDL Number
MFCD02094728
PubChem ID
4985744
Melting Point
117 - 122 ?C
Appearance
Blanc cassé uni
Conditions
Magasin chez RT
General Information
Synonyms
Acide 2-fluoro-3-méthoxybenzèneboronique
CAS Number
352303-67-4
Purity
≥ 99,5 % (HPLC)
Molecular Formula
C 7 H 8 BFO 3
Molecular Weight
169.95
MDL Number
MFCD02094728
PubChem ID
4985744
Melting Point
117 - 122 ?C
Appearance
Blanc cassé uni
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-Fluoro-3-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 drugs targeting cancer and other diseases. Its unique structure allows for the modification of biological activity, making it valuable in drug discovery.
  • Organic Synthesis: It is frequently used in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for forming carbon-carbon bonds. This application is crucial in creating complex organic molecules, thereby enhancing the efficiency of synthetic pathways.
  • Material Science: The compound is employed in the development of advanced materials, including polymers and nanomaterials. Its boronic acid functionality allows for the formation of dynamic covalent bonds, which can improve material properties like strength and flexibility.
  • Bioconjugation: In biochemistry, it is utilized for the modification of biomolecules, enabling the attachment of various functional groups. This application is particularly important in creating targeted drug delivery systems and diagnostic tools.
  • Analytical Chemistry: It is used in the development of sensors and assays for detecting specific biomolecules. The ability to form stable complexes with certain analytes enhances the sensitivity and selectivity of these analytical methods.

Citations