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Catalog Number:
40097
CAS Number:
364044-44-0
Acide 4'-chloro-4-biphénylboronique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide (4'-chloro-[1,1'-biphényl]-4-yl)boronique
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Product Information

4'-Chloro-4-biphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals appreciate its effectiveness in the development of pharmaceuticals, agrochemicals, and advanced materials. The compound's unique chlorophenyl group enhances its reactivity, allowing for the efficient construction of complex molecular architectures.

In addition to its synthetic applications, 4'-Chloro-4-biphenylboronic acid has shown promise in the field of sensor technology, particularly in the detection of biomolecules. Its ability to selectively bind to specific targets opens avenues for innovative diagnostic tools. With its robust performance and adaptability, this compound stands out as a valuable asset for researchers aiming to push the boundaries of chemical synthesis and application.

Synonyms
Acide (4'-chloro-[1,1'-biphényl]-4-yl)boronique
CAS Number
364044-44-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C12H10BClO2
Molecular Weight
232.47
MDL Number
MFCD08544389
PubChem ID
16244482
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide (4'-chloro-[1,1'-biphényl]-4-yl)boronique
CAS Number
364044-44-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C12H10BClO2
Molecular Weight
232.47
MDL Number
MFCD08544389
PubChem ID
16244482
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4'-Chloro-4-biphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki coupling reactions, allowing chemists to create complex organic molecules efficiently. Its ability to form stable bonds with various substrates makes it valuable in developing pharmaceuticals and agrochemicals.
  • Drug Development: In medicinal chemistry, it is used to modify drug candidates, improving their efficacy and selectivity. The presence of the boronic acid group can enhance the interaction with biological targets, leading to more effective treatments.
  • Material Science: The compound is applied in the development of advanced materials, such as polymers and nanomaterials. Its unique properties contribute to the creation of materials with enhanced mechanical and thermal stability.
  • Bioconjugation: It plays a significant role in bioconjugation processes, where it is used to attach biomolecules to surfaces or other molecules. This application is crucial in the development of biosensors and targeted drug delivery systems.
  • Environmental Chemistry: The compound is utilized in the detection and removal of pollutants. Its reactivity allows for the development of sensors that can identify environmental contaminants, aiding in pollution control efforts.

Citations