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Catalog Number:
40175
CAS Number:
78887-39-5
Acide 3-acétamidophénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-acétamidobenzèneboronique
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Product Information

3-Acetamidophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a unique acetamido group that enhances its reactivity and selectivity in various chemical reactions, making it an essential building block for the development of pharmaceuticals and agrochemicals. Its ability to form stable complexes with diols allows for its application in the synthesis of complex organic molecules, including those used in drug discovery and development.

In addition to its synthetic applications, 3-Acetamidophenylboronic acid has shown promise in the field of biochemistry, particularly in the design of targeted therapies and diagnostic agents. Researchers appreciate its role in the development of boron-containing compounds that can selectively bind to biomolecules, facilitating the study of biological processes and disease mechanisms. The compound's favorable properties, such as its solubility and stability, further enhance its utility in laboratory settings, making it a valuable asset for both academic and industrial research.

Synonyms
Acide 3-acétamidobenzèneboronique
CAS Number
78887-39-5
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C8H10BNO3
Molecular Weight
178.98
MDL Number
MFCD00236013
PubChem ID
157274
Melting Point
140 °C (lit.)
Appearance
Poudre cristalline orange clair à jaune à verte
Conditions
Magasin chez RT
General Information
Synonyms
Acide 3-acétamidobenzèneboronique
CAS Number
78887-39-5
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C8H10BNO3
Molecular Weight
178.98
MDL Number
MFCD00236013
PubChem ID
157274
Melting Point
140 °C (lit.)
Appearance
Poudre cristalline orange clair à jaune à verte
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-Acetamidophenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound is often used in the synthesis of pharmaceuticals, particularly in the development of anti-cancer agents, due to its ability to form stable complexes with biomolecules.
  • Bioconjugation: It serves as a versatile building block for bioconjugation, allowing researchers to attach drugs or imaging agents to proteins, enhancing targeted delivery in therapeutic applications.
  • Organic Synthesis: The compound plays a significant role in cross-coupling reactions, which are essential in creating complex organic molecules, making it valuable in the production of agrochemicals and fine chemicals.
  • Sensor Technology: It is employed in the development of chemical sensors, particularly for detecting glucose levels, benefiting the medical field by aiding in diabetes management.
  • Material Science: This compound is used in the formulation of advanced materials, such as polymers and coatings, which require specific chemical properties for improved performance in various applications.

Citations