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Catalog Number:
40138
CAS Number:
145240-28-4
Ácido 4-butilfenilborónico
Purity:
95 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 4-butilbencenoborónico
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$46.77 /1G
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Product Information

4-Butylphenylboronic acid is a versatile organoboron compound known for its significant role in organic synthesis and medicinal chemistry. This compound features a boronic acid functional group, which allows it to participate in various reactions, including Suzuki coupling, a widely used method for forming carbon-carbon bonds. Its unique structure, characterized by the butyl group, enhances its solubility in organic solvents, making it an excellent choice for researchers working in diverse environments.

In the pharmaceutical industry, 4-Butylphenylboronic acid is utilized in the development of biologically active compounds, particularly in the synthesis of complex molecules that can lead to new drug discoveries. Its ability to form stable complexes with diols also makes it valuable in sensor applications and materials science. Researchers appreciate its efficiency and effectiveness in facilitating reactions, providing a reliable option for those looking to streamline their synthetic processes. With its broad applicability and favorable properties, 4-Butylphenylboronic acid stands out as a crucial tool for chemists and industry professionals alike.

Synonyms
Ácido 4-butilbencenoborónico
CAS Number
145240-28-4
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C 10 H 15 BO 2
Molecular Weight
178.04
MDL Number
MFCD02093926
PubChem ID
4100860
Melting Point
97 °C (Literatura)
Appearance
Polvo cristalino de color blanco a naranja.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 4-butilbencenoborónico
CAS Number
145240-28-4
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C 10 H 15 BO 2
Molecular Weight
178.04
MDL Number
MFCD02093926
PubChem ID
4100860
Melting Point
97 °C (Literatura)
Appearance
Polvo cristalino de color blanco a naranja.
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

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

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules.
  • Pharmaceutical Development: It is used in the development of boron-containing pharmaceuticals, which can enhance the efficacy of drug compounds through improved targeting and reduced side effects.
  • Material Science: The compound is employed in creating advanced materials, such as polymers and nanocomposites, which exhibit enhanced mechanical and thermal properties.
  • Bioconjugation: It plays a role in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, facilitating the development of biosensors and targeted drug delivery systems.
  • Environmental Applications: This chemical is also explored for its potential in environmental remediation, particularly in the removal of pollutants through boron-based adsorption techniques.

Citas