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Catalog Number:
40173
CAS Number:
22237-13-4
Acide 4-éthoxyphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 4-éthoxybenzèneboronique
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Product Information

4-Ethoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. 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 pharmaceuticals, agrochemicals, and advanced materials. Its effectiveness in facilitating the formation of carbon-carbon bonds allows for the synthesis of complex molecules, which is crucial in drug discovery and development.

In addition to its synthetic applications, 4-Ethoxyphenylboronic acid serves as a valuable tool in the field of sensor technology, particularly in the detection of glucose and other biomolecules. Its selectivity and sensitivity make it an attractive option for developing diagnostic devices. With its broad range of applications, this compound stands out for its efficiency and reliability, providing researchers with a powerful resource for innovative solutions in various fields.

Synonyms
Acide 4-éthoxybenzèneboronique
CAS Number
22237-13-4
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 11 BO 3
Molecular Weight
165.98
MDL Number
MFCD00674028
PubChem ID
2734351
Melting Point
168 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Magasin chez RT
General Information
Synonyms
Acide 4-éthoxybenzèneboronique
CAS Number
22237-13-4
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 11 BO 3
Molecular Weight
165.98
MDL Number
MFCD00674028
PubChem ID
2734351
Melting Point
168 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
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-Ethoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in the Suzuki-Miyaura coupling reaction, which is essential for forming carbon-carbon bonds. This application is particularly valuable in the pharmaceutical industry for developing complex drug molecules.
  • Bioconjugation: It is used to attach biomolecules to surfaces or other molecules, enhancing the functionality of biosensors and drug delivery systems. This is crucial in the field of biochemistry and molecular biology.
  • Material Science: The compound plays a role in creating advanced materials, such as polymers and nanomaterials, which have applications in electronics and coatings. Its ability to form stable complexes with various substrates makes it a versatile choice.
  • Diagnostics: In medical research, it is utilized in the development of diagnostic tools, particularly in detecting specific biomolecules. This application is vital for early disease detection and monitoring.
  • Environmental Chemistry: It helps in the detection and removal of pollutants, as it can form complexes with heavy metals. This application is significant for environmental monitoring and remediation efforts.

Citations