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Catalog Number:
40182
CAS Number:
90555-66-1
Acide 3-éthoxyphénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-éthoxybenzèneboronique
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Product Information

3-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 often 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 organic molecules, which is crucial in drug discovery and development.

In addition to its synthetic applications, 3-Ethoxyphenylboronic acid serves as a valuable tool in the field of biochemistry, where it is used to study carbohydrate recognition and enzyme activity. Its ability to selectively bind to specific biomolecules enhances its relevance in the development of targeted therapies and diagnostic tools. With its broad range of applications and unique reactivity, this compound is an indispensable asset for researchers aiming to innovate in various fields, including pharmaceuticals and materials science.

Synonyms
Acide 3-éthoxybenzèneboronique
CAS Number
90555-66-1
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 11 BO 3
Molecular Weight
165.98
MDL Number
MFCD00274219
PubChem ID
2773920
Melting Point
153 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Magasin chez RT
General Information
Synonyms
Acide 3-éthoxybenzèneboronique
CAS Number
90555-66-1
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 11 BO 3
Molecular Weight
165.98
MDL Number
MFCD00274219
PubChem ID
2773920
Melting Point
153 °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

3-Ethoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in the synthesis of complex organic molecules.
  • Pharmaceutical Development: It plays a critical role in drug discovery, particularly in the development of boron-containing pharmaceuticals that can target specific biological pathways.
  • Material Science: Used in the fabrication of advanced materials, including polymers and nanomaterials, enhancing their properties such as conductivity and mechanical strength.
  • Bioconjugation: This chemical is effective in linking biomolecules, aiding in the development of targeted therapies and diagnostic tools in the biomedical field.
  • Analytical Chemistry: It is utilized in the preparation of sensor materials for detecting various analytes, providing high sensitivity and selectivity in environmental monitoring and food safety applications.

Citations