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Catalog Number:
40336
CAS Number:
73852-18-3
2,4,6-Trichlorophenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
2,4,6-Trichlorobenzeneboronic acid
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Product Information

2,4,6-Trichlorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique chlorinated structure enhances its reactivity and selectivity, allowing researchers to create complex organic molecules with precision. This compound is particularly valuable in the development of pharmaceuticals, agrochemicals, and advanced materials, where it serves as a key building block for various chemical transformations.

Moreover, 2,4,6-Trichlorophenylboronic acid has shown potential in the field of sensor technology, where it can be employed to detect specific biomolecules due to its affinity for hydroxyl groups. Its applications extend to the synthesis of biologically active compounds, making it a crucial tool for researchers aiming to innovate in drug discovery and development. With its robust performance in diverse applications, this compound stands out as a reliable choice for professionals seeking efficiency and effectiveness in their chemical processes.

Synonyms
2,4,6-Trichlorobenzeneboronic acid
CAS Number
73852-18-3
Purity
98 - 105% (Assay by titration)
Molecular Formula
C6H4BCl3O2
Molecular Weight
225.26
MDL Number
MFCD01074621
PubChem ID
2734384
Melting Point
164 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
2,4,6-Trichlorobenzeneboronic acid
CAS Number
73852-18-3
Purity
98 - 105% (Assay by titration)
Molecular Formula
C6H4BCl3O2
Molecular Weight
225.26
MDL Number
MFCD01074621
PubChem ID
2734384
Melting Point
164 °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

2,4,6-Trichlorophenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals, enhancing the efficiency of chemical reactions.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds, making it invaluable in materials science and drug discovery.
  • Bioconjugation: The boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation techniques for labeling biomolecules, aiding in the development of targeted therapies and diagnostics.
  • Environmental Applications: It can be employed in the detection and removal of pollutants, such as phenolic compounds, from wastewater, contributing to environmental sustainability efforts.
  • Sensor Development: This compound is utilized in creating sensors for detecting glucose and other biomolecules, which is particularly beneficial in the medical field for diabetes management.

Citations