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Catalog Number:
40132
CAS Number:
149104-90-5
4-Acetylphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
4-Acetylbenzeneboronic acid
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Product Information

4-Acetylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a phenyl ring with an acetyl group, making it an essential building block for the development of various pharmaceuticals and agrochemicals. Its unique ability to form reversible covalent bonds with diols enhances its application in the synthesis of complex molecules, particularly in the field of drug discovery and development. Researchers often leverage its properties in the design of targeted therapies, where it plays a crucial role in the synthesis of biologically active compounds.

In addition to its applications in pharmaceuticals, 4-Acetylphenylboronic acid is also valuable in materials science, particularly in the development of sensors and catalysts. Its reactivity with sugars and other biomolecules allows for innovative approaches in biosensing technologies. The compound's stability and ease of handling make it an attractive choice for both laboratory and industrial applications, providing researchers and professionals with a reliable tool for advancing their projects.

Synonyms
4-Acetylbenzeneboronic acid
CAS Number
149104-90-5
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H9BO3
Molecular Weight
163.97
MDL Number
MFCD01074667
PubChem ID
3702122
Melting Point
239 °C (Lit.)
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Acetylbenzeneboronic acid
CAS Number
149104-90-5
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H9BO3
Molecular Weight
163.97
MDL Number
MFCD01074667
PubChem ID
3702122
Melting Point
239 °C (Lit.)
Appearance
White to light yellow crystalline 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-Acetylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, facilitating the formation of carbon-boron bonds that are crucial in creating complex organic molecules.
  • Bioconjugation: It is employed in bioconjugation reactions, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in drug delivery systems and diagnostic applications.
  • Fluorescent Probes: The compound is used in developing fluorescent probes for sensing applications, particularly in detecting specific ions or biomolecules, enhancing the sensitivity and specificity of assays.
  • Material Science: In material science, it plays a role in the development of boron-containing polymers, which can exhibit unique properties such as improved thermal stability and mechanical strength.
  • Chemical Sensors: 4-Acetylphenylboronic acid is utilized in the design of chemical sensors for detecting sugars and other analytes, providing a reliable method for monitoring various biological and environmental samples.

Citations