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Catalog Number:
31428
CAS Number:
51067-38-0
4-Phenoxyphenylboronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
4-Phenoxybenzeneboronic acid, p-Phenoxyphenylboronic acid
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Product Information

4-Phenoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form reversible covalent bonds with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique structure allows for applications in the synthesis of complex organic molecules, including those used in drug discovery and development. Researchers particularly value its role in Suzuki-Miyaura cross-coupling reactions, which are pivotal in creating biaryl compounds that serve as key intermediates in the production of advanced materials and biologically active molecules.

Additionally, 4-Phenoxyphenylboronic acid exhibits significant potential in the field of sensor technology, where it can be employed in the detection of glucose and other biomolecules due to its selective binding properties. Its compatibility with various solvents and stability under different conditions further enhance its appeal for industrial applications. With its broad range of uses, this compound stands out as a valuable tool for researchers and industry professionals seeking efficient and effective solutions in their projects.

Synonyms
4-Phenoxybenzeneboronic acid, p-Phenoxyphenylboronic acid
CAS Number
51067-38-0
Purity
≥ 99% (HPLC)
Molecular Formula
C12H11BO3
Molecular Weight
214.03
MDL Number
MFCD00093312
PubChem ID
2734377
Melting Point
141-145 ?C
Appearance
White to off-white powder
Conditions
Store at RT
General Information
Synonyms
4-Phenoxybenzeneboronic acid, p-Phenoxyphenylboronic acid
CAS Number
51067-38-0
Purity
≥ 99% (HPLC)
Molecular Formula
C12H11BO3
Molecular Weight
214.03
MDL Number
MFCD00093312
PubChem ID
2734377
Melting Point
141-145 ?C
Appearance
White to off-white 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-Phenoxyphenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in creating targeted therapies for cancer treatment.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which allows for the formation of complex organic molecules, enhancing the efficiency of chemical synthesis.
  • Material Science: The compound is used in developing advanced materials, including polymers and nanomaterials, which have applications in electronics and coatings.
  • Bioconjugation: It plays a significant role in bioconjugation techniques, aiding in the attachment of biomolecules to surfaces or other molecules, which is crucial for biosensors and drug delivery systems.
  • Analytical Chemistry: 4-Phenoxyphenylboronic acid is utilized in various analytical methods, including chromatography, to improve the separation and detection of compounds, making it valuable for quality control in pharmaceuticals.

Citations