Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
31086
CAS Number:
5122-94-1
Acide 4-biphénylboronique (contient des quantités variables d'anhydride)
Purity:
≥ 99 % (HPLC)
Synonym(s):
Acide biphényl-4-boronique (contient des quantités variables d'anhydride), Acide 4-phénylphénylboronique (contient des quantités variables d'anhydride)
Documents
$18.53 /5G
Taille
Request Bulk Quote
Product Information

Conserver à l'abri des agents oxydants forts, des sources d'inflammation.

Synonyms
Acide biphényl-4-boronique (contient des quantités variables d'anhydride), Acide 4-phénylphénylboronique (contient des quantités variables d'anhydride)
CAS Number
5122-94-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C 12 H 11 BO 2
Molecular Weight
198.03
MDL Number
MFCD00093311
PubChem ID
151253
Melting Point
232 - 245 ?C
Appearance
Blanc cassé uni
Conditions
Magasin chez RT
General Information
Synonyms
Acide biphényl-4-boronique (contient des quantités variables d'anhydride), Acide 4-phénylphénylboronique (contient des quantités variables d'anhydride)
CAS Number
5122-94-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C 12 H 11 BO 2
Molecular Weight
198.03
MDL Number
MFCD00093311
PubChem ID
151253
Melting Point
232 - 245 ?C
Appearance
Blanc cassé uni
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
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.

Citations