Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
40057
CAS Number:
253342-48-2
4,4,5,5-Tetramethyl-2-(m-tolyl)-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)toluene, m-Tolylboronic acid pinacol ester
Documents
$32.25 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

4,4,5,5-Tetramethyl-2-(m-tolyl)-1,3,2-dioxaborolane is a versatile organoboron compound that has garnered attention in various fields, particularly in organic synthesis and materials science. This compound is recognized for its unique dioxaborolane structure, which enhances its stability and reactivity, making it an excellent candidate for applications in cross-coupling reactions and as a boron source in organic transformations. Its ability to facilitate the formation of carbon-carbon bonds is particularly valuable in the development of pharmaceuticals and agrochemicals, where precision and efficiency are paramount.

Moreover, 4,4,5,5-Tetramethyl-2-(m-tolyl)-1,3,2-dioxaborolane is also utilized in the synthesis of advanced materials, including polymers and nanomaterials, due to its favorable electronic properties. Researchers appreciate its compatibility with various reaction conditions, allowing for greater flexibility in experimental design. This compound stands out for its ease of handling and storage, making it a practical choice for both laboratory and industrial applications. With its broad range of uses, it is an essential tool for chemists aiming to innovate in synthetic methodologies and material development.

Synonyms
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)toluene, m-Tolylboronic acid pinacol ester
CAS Number
253342-48-2
Purity
≥ 98% (GC)
Molecular Formula
C13H19BO2
Molecular Weight
218.1
MDL Number
MFCD05864303
PubChem ID
2760598
Melting Point
34 - 38 °C
Appearance
White to off-white powder to lump
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)toluene, m-Tolylboronic acid pinacol ester
CAS Number
253342-48-2
Purity
≥ 98% (GC)
Molecular Formula
C13H19BO2
Molecular Weight
218.1
MDL Number
MFCD05864303
PubChem ID
2760598
Melting Point
34 - 38 °C
Appearance
White to off-white powder to lump
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4,4,5,5-Tetramethyl-2-(m-tolyl)-1,3,2-dioxaborolane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, particularly in the formation of carbon-boron bonds, which are crucial for synthesizing complex organic molecules.
  • Drug Development: Its unique properties make it valuable in pharmaceutical research, aiding in the design and synthesis of new drug candidates, especially in targeting specific biological pathways.
  • Material Science: The compound is used in the development of advanced materials, including polymers and coatings, enhancing their properties such as durability and resistance to environmental factors.
  • Bioconjugation: It plays a role in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of biosensors and targeted drug delivery systems.
  • Environmental Applications: This chemical can be employed in environmental chemistry for the detection and removal of pollutants, contributing to cleaner and safer ecosystems.

Citations