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Catalog Number:
31086
CAS Number:
5122-94-1
Ácido 4-bifenilborónico (contiene cantidades variables de anhídrido)
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ácido bifenil-4-borónico (contiene cantidades variables de anhídrido), Ácido 4-fenilfenilborónico (contiene cantidades variables de anhídrido)
Documents
$18.53 /5G
Tamaño
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Product Information

Conservar lejos de agentes oxidantes y fuentes de ignición.

Synonyms
Ácido bifenil-4-borónico (contiene cantidades variables de anhídrido), Ácido 4-fenilfenilborónico (contiene cantidades variables de anhídrido)
CAS Number
5122-94-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H11BO2
Molecular Weight
198.03
MDL Number
MFCD00093311
PubChem ID
151253
Melting Point
232 - 245 ?C
Appearance
Sólido de color blanquecino
Conditions
Tienda en RT
General Information
Synonyms
Ácido bifenil-4-borónico (contiene cantidades variables de anhídrido), Ácido 4-fenilfenilborónico (contiene cantidades variables de anhídrido)
CAS Number
5122-94-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H11BO2
Molecular Weight
198.03
MDL Number
MFCD00093311
PubChem ID
151253
Melting Point
232 - 245 ?C
Appearance
Sólido de color blanquecino
Conditions
Tienda en RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Biphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in the Suzuki-Miyaura cross-coupling reaction, enabling the formation of carbon-carbon bonds, which is essential for creating complex organic molecules.
  • Pharmaceutical Development: It is used in the synthesis of various pharmaceuticals, particularly in the development of antitumor agents and other therapeutic compounds, enhancing drug efficacy and specificity.
  • Material Science: The compound plays a role in the development of advanced materials, such as polymers and nanomaterials, due to its ability to form stable complexes with various substrates.
  • Bioconjugation: Its boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation techniques for labeling biomolecules, which is crucial in diagnostics and research.
  • Environmental Applications: 4-Biphenylboronic acid is explored for use in sensors that detect environmental pollutants, providing a means to monitor and mitigate contamination effectively.

Citas