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Catalog Number:
40133
CAS Number:
177490-82-3
4-Acetoxyphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-Acetoxybenzeneboronic acid
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$39.56 /200MG
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Product Information

4-Acetoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a phenyl ring substituted with an acetoxy group, enhancing its reactivity and solubility in various solvents. Its unique structure allows it to participate in Suzuki-Miyaura cross-coupling reactions, making it invaluable for the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Researchers and industry professionals can leverage this compound for the development of pharmaceuticals, agrochemicals, and advanced materials, where precise molecular architecture is essential.

In addition to its role in synthetic chemistry, 4-Acetoxyphenylboronic acid exhibits potential in biological applications, particularly in the design of targeted drug delivery systems and as a building block for biologically active compounds. Its ability to form reversible covalent bonds with diols makes it a candidate for creating innovative therapeutic agents. The compound's favorable properties, such as stability and ease of handling, further enhance its appeal for both laboratory and industrial applications, making it a valuable addition to any chemical toolkit.

Synonyms
4-Acetoxybenzeneboronic acid
CAS Number
177490-82-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H9BO4
Molecular Weight
179.97
MDL Number
MFCD09027198
PubChem ID
44119577
Melting Point
224 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
4-Acetoxybenzeneboronic acid
CAS Number
177490-82-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H9BO4
Molecular Weight
179.97
MDL Number
MFCD09027198
PubChem ID
44119577
Melting Point
224 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Organic Synthesis: This compound serves as a versatile building block for synthesizing various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: Its boronic acid functionality allows for the formation of reversible covalent bonds with diols, making it useful in designing targeted drug delivery systems and enhancing the efficacy of certain medications.
  • Bioconjugation: Researchers employ this chemical in bioconjugation processes to attach biomolecules to surfaces or other molecules, facilitating the development of biosensors and diagnostic tools.
  • Material Science: It is used in creating advanced materials, such as polymers and hydrogels, which have applications in drug release and tissue engineering due to their unique properties.
  • Chemical Sensors: The compound is instrumental in developing chemical sensors that can detect specific biomolecules, contributing to advancements in medical diagnostics and environmental monitoring.

Citations