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Catalog Number:
40329
CAS Number:
862248-93-9
3,4,5-Trichlorophenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
3,4,5-Trichlorobenzeneboronic acid
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Product Information

3,4,5-Trichlorophenylboronic acid is a versatile compound that plays a crucial role in various chemical synthesis applications, particularly in the field of organic chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in the development of pharmaceuticals and agrochemicals. Its unique structure allows for selective functionalization, which is beneficial in the synthesis of complex organic molecules. Researchers utilize 3,4,5-Trichlorophenylboronic acid in Suzuki coupling reactions, enabling the formation of carbon-carbon bonds that are vital for constructing intricate molecular architectures.

In addition to its applications in synthetic chemistry, this compound is also valuable in materials science, where it can be used to modify surfaces and enhance the properties of polymers. Its high reactivity and specificity make it a preferred choice for chemists looking to optimize their synthetic pathways. With its proven efficacy and adaptability, 3,4,5-Trichlorophenylboronic acid stands out as a key player in advancing research and industrial processes.

Synonyms
3,4,5-Trichlorobenzeneboronic acid
CAS Number
862248-93-9
Purity
98 - 105% (Assay by titration)
Molecular Formula
C6H4BCl3O2
Molecular Weight
225.26
MDL Number
MFCD03095126
PubChem ID
24820465
Melting Point
> 360 °C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3,4,5-Trichlorobenzeneboronic acid
CAS Number
862248-93-9
Purity
98 - 105% (Assay by titration)
Molecular Formula
C6H4BCl3O2
Molecular Weight
225.26
MDL Number
MFCD03095126
PubChem ID
24820465
Melting Point
> 360 °C
Appearance
White to off-white 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

3,4,5-Trichlorophenylboronic 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, allowing researchers to create complex molecules efficiently.
  • Bioconjugation: It is used in bioconjugation reactions, where it helps attach biomolecules to surfaces or other molecules, enhancing the development of targeted drug delivery systems.
  • Sensor Development: The compound is employed in the fabrication of chemical sensors, particularly for detecting phenolic compounds, which is crucial in environmental monitoring and safety assessments.
  • Material Science: It plays a role in the development of advanced materials, such as polymers and coatings, that require specific chemical properties for improved performance in various applications.
  • Medicinal Chemistry: Researchers leverage its unique properties to design and optimize new therapeutic agents, particularly in cancer research, where targeted treatments are essential.

Citations