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Catalog Number:
40152
CAS Number:
393870-04-7
Acide 4'-méthyl-4-biphénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide (4'-méthyl-[1,1'-biphényl]-4-yl)boronique
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Product Information

4'-Methyl-4-biphenylboronic acid is a versatile organoboron compound that plays a crucial role in various chemical applications, particularly in organic synthesis and medicinal chemistry. This compound 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 utilize this compound to facilitate the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure allows for enhanced reactivity and selectivity, which can lead to improved yields in synthetic processes compared to other boronic acids.

In addition to its synthetic utility, 4'-Methyl-4-biphenylboronic acid is also employed in the development of sensors and as a building block for functional materials. Its properties make it suitable for applications in catalysis and polymer chemistry, where it can contribute to the design of novel materials with specific functionalities. The compound's stability and ease of handling further enhance its appeal, making it a valuable addition to any laboratory focused on innovative chemical research.

Synonyms
Acide (4'-méthyl-[1,1'-biphényl]-4-yl)boronique
CAS Number
393870-04-7
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 13 H 13 BO 2
Molecular Weight
212.06
MDL Number
MFCD04038170
PubChem ID
23005380
Melting Point
138 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide (4'-méthyl-[1,1'-biphényl]-4-yl)boronique
CAS Number
393870-04-7
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 13 H 13 BO 2
Molecular Weight
212.06
MDL Number
MFCD04038170
PubChem ID
23005380
Melting Point
138 °C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
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

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

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex organic molecules efficiently. Its ability to form stable complexes with various substrates enhances reaction yields.
  • Pharmaceutical Development: In drug discovery, it is used to develop boron-containing compounds that can exhibit unique biological activities, potentially leading to new therapeutic agents for various diseases.
  • Material Science: This chemical is applied in the synthesis of advanced materials, including polymers and nanomaterials, which can be utilized in electronics and photonics due to their unique electronic properties.
  • Bioconjugation: It plays a role in bioconjugation chemistry, where it can be used to attach biomolecules to surfaces or other molecules, facilitating the development of biosensors and targeted drug delivery systems.
  • Environmental Applications: The compound is explored for its potential in environmental remediation, particularly in the removal of pollutants through the formation of stable complexes with heavy metals.

Citations