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Catalog Number:
40105
CAS Number:
105365-51-3
Ácido 4-butoxifenilborónico
Purity:
95 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 4-butoxibencenoborónico
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Product Information

4-Butoxyphenylboronic 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 the development of various pharmaceuticals and agrochemicals. Its unique properties allow for the selective functionalization of aromatic compounds, facilitating the synthesis of complex molecules with precision. Researchers often leverage 4-butoxyphenylboronic acid in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the creation of biaryl compounds, a class of compounds with significant applications in drug discovery and material science.

The compound's solubility in organic solvents enhances its usability in diverse laboratory settings, while its relatively low toxicity makes it a safer alternative compared to other boronic acids. Additionally, 4-butoxyphenylboronic acid's stability under various conditions allows for its application in both academic research and industrial processes. Its role in the synthesis of advanced materials and pharmaceuticals underscores its importance in the chemical industry, providing researchers with a reliable tool for innovative solutions.

Synonyms
Ácido 4-butoxibencenoborónico
CAS Number
105365-51-3
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C 10 H 15 BO 3
Molecular Weight
194.04
MDL Number
MFCD03427054
PubChem ID
3836310
Melting Point
108 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 4-butoxibencenoborónico
CAS Number
105365-51-3
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C 10 H 15 BO 3
Molecular Weight
194.04
MDL Number
MFCD03427054
PubChem ID
3836310
Melting Point
108 °C (Literatura)
Appearance
Polvo cristalino de color blanco a blanquecino.
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-Butoxyphenylboronic 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.
  • Pharmaceutical Development: It is employed in the synthesis of boron-containing drugs, which can enhance the efficacy of treatments for various diseases, including cancer.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and nanomaterials, that exhibit unique properties for applications in electronics and optics.
  • Bioconjugation: It plays a role in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial for drug delivery systems.
  • Analytical Chemistry: This chemical is utilized in sensor development, particularly in detecting biomolecules, due to its ability to form stable complexes with various analytes.

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