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Catalog Number:
40348
CAS Number:
5980-97-2
2,4,6-Trimethylphenylboronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
2-Mesityleneboronic acid, 2,4,6-Trimethylbenzeneboronic acid
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Product Information

2,4,6-Trimethylphenylboronic acid is a versatile organoboron compound known for its significant role in organic synthesis and medicinal chemistry. This compound features a boronic acid functional group, which makes it an essential reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. Its unique structure allows for selective binding with diols, making it valuable in the development of sensors and in the synthesis of complex organic molecules. Researchers and industry professionals utilize 2,4,6-Trimethylphenylboronic acid in the production of pharmaceuticals, agrochemicals, and advanced materials, where precision and efficiency are paramount.

The compound's high reactivity and stability under various conditions enhance its applicability in diverse fields, including polymer science and catalysis. Its ability to form stable complexes with various substrates opens avenues for innovative applications in drug discovery and development. With its favorable properties, 2,4,6-Trimethylphenylboronic acid stands out as a crucial tool for chemists seeking to streamline their synthetic processes while achieving high yields and purity.

Synonyms
2-Mesityleneboronic acid, 2,4,6-Trimethylbenzeneboronic acid
CAS Number
5980-97-2
Purity
≥ 98% (HPLC)
Molecular Formula
C9H13BO2
Molecular Weight
164.01
MDL Number
MFCD00236060
PubChem ID
292184
Melting Point
115 - 122 °C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-Mesityleneboronic acid, 2,4,6-Trimethylbenzeneboronic acid
CAS Number
5980-97-2
Purity
≥ 98% (HPLC)
Molecular Formula
C9H13BO2
Molecular Weight
164.01
MDL Number
MFCD00236060
PubChem ID
292184
Melting Point
115 - 122 °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

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

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which is essential for creating complex organic molecules.
  • Pharmaceutical Development: It plays a significant role in drug discovery, particularly in the synthesis of biologically active compounds, enhancing the efficiency of developing new medications.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and nanomaterials, due to its ability to modify surface properties and improve material performance.
  • Sensor Technology: Its unique properties make it suitable for creating sensors that detect specific biomolecules, which is crucial in medical diagnostics and environmental monitoring.
  • Bioconjugation: This boronic acid derivative is utilized in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the functionality of biosensors and drug delivery systems.

Citations