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

Conservar alejado de sustancias incompatibles, fuentes de ignición y agentes oxidantes. Evitar periodos de almacenamiento prolongados.

Synonyms
Ácido 2-fluoro-3-metoxibencenoborónico
CAS Number
352303-67-4
Purity
≥ 99,5 % (HPLC)
Molecular Formula
C7H8BFO3
Molecular Weight
169.95
MDL Number
MFCD02094728
PubChem ID
4985744
Melting Point
117 - 122 ?C
Appearance
Sólido de color blanquecino
Conditions
Tienda en RT
General Information
Synonyms
Ácido 2-fluoro-3-metoxibencenoborónico
CAS Number
352303-67-4
Purity
≥ 99,5 % (HPLC)
Molecular Formula
C7H8BFO3
Molecular Weight
169.95
MDL Number
MFCD02094728
PubChem ID
4985744
Melting Point
117 - 122 ?C
Appearance
Sólido de color blanquecino
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
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.

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