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Catalog Number:
40176
CAS Number:
105365-50-2
4-Hexylphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-Hexylbenzeneboronic acid
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Product Information

4-Hexylphenylboronic acid is a versatile compound widely utilized in organic synthesis and materials science. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals leverage its unique properties to develop advanced materials, pharmaceuticals, and agrochemicals. Its hydrophobic nature allows for effective incorporation into various organic matrices, enhancing the performance of polymeric materials and improving the solubility of active pharmaceutical ingredients.

In addition to its role in synthetic chemistry, 4-Hexylphenylboronic acid is also employed in sensor technology, where it can be used to detect sugars and other biomolecules through selective binding. This compound's ability to function in diverse environments and its compatibility with various substrates make it an attractive choice for researchers looking to innovate in fields such as drug delivery systems and environmental monitoring. With its robust performance and multifunctional applications, 4-Hexylphenylboronic acid stands out as a valuable tool for advancing scientific research and industrial processes.

Synonyms
4-Hexylbenzeneboronic acid
CAS Number
105365-50-2
Purity
97 - 105% (Assay by titration)
Molecular Formula
C12H19BO2
Molecular Weight
206.09
MDL Number
MFCD04039029
PubChem ID
4197864
Melting Point
81 - 84 °C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Hexylbenzeneboronic acid
CAS Number
105365-50-2
Purity
97 - 105% (Assay by titration)
Molecular Formula
C12H19BO2
Molecular Weight
206.09
MDL Number
MFCD04039029
PubChem ID
4197864
Melting Point
81 - 84 °C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Materials Science: It is used to create advanced materials, including polymers and nanomaterials, enhancing properties like conductivity and strength.
  • Bioconjugation: In biochemistry, it aids in the modification of biomolecules, allowing for the attachment of various functional groups to proteins and nucleic acids for drug delivery systems.
  • Sensor Development: The compound is instrumental in developing sensors for detecting biomolecules, offering high sensitivity and selectivity, which is crucial in medical diagnostics.
  • Environmental Applications: It can be applied in the detection and removal of pollutants, showcasing its utility in environmental chemistry and sustainability efforts.

Citations