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Catalog Number:
39912
CAS Number:
401797-00-0
2-(3,4-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-o-xylene, 3,4-Dimethylphenylboronic acid pinacol ester
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Product Information

2-(3,4-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile boron-containing compound known for its unique structural properties and reactivity. This compound is particularly valuable in organic synthesis, serving as a key intermediate in the development of pharmaceuticals and agrochemicals. Its ability to participate in cross-coupling reactions makes it an essential reagent for chemists looking to create complex molecular architectures efficiently. Additionally, its stability and compatibility with various reaction conditions enhance its utility in diverse chemical processes.

Researchers and industry professionals can leverage this compound in the synthesis of biologically active molecules, including potential drug candidates. Its favorable properties allow for improved yields and selectivity in reactions, making it a preferred choice over similar compounds. Whether in academic research or industrial applications, 2-(3,4-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane stands out for its effectiveness and reliability in advancing chemical innovation.

Synonyms
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-o-xylene, 3,4-Dimethylphenylboronic acid pinacol ester
CAS Number
401797-00-0
Purity
≥ 98% (GC)
Molecular Formula
C14H21BO2
Molecular Weight
232.13
MDL Number
MFCD12405519
PubChem ID
15906194
Melting Point
35 ?C (Lit.)
Appearance
White to off white powder to lump
Conditions
Store at 2 - 8 °C
General Information
Synonyms
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-o-xylene, 3,4-Dimethylphenylboronic acid pinacol ester
CAS Number
401797-00-0
Purity
≥ 98% (GC)
Molecular Formula
C14H21BO2
Molecular Weight
232.13
MDL Number
MFCD12405519
PubChem ID
15906194
Melting Point
35 ?C (Lit.)
Appearance
White to off white powder to lump
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-(3,4-Dimethylphenyl)-4,4,5,5-tetramethyl-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 synthesis of complex organic molecules, enabling researchers to create new compounds with desired properties.
  • Pharmaceutical Development: It plays a crucial role in drug discovery, where it is used to modify drug candidates, enhancing their efficacy and bioavailability in medicinal chemistry.
  • Material Science: The compound is utilized in the development of advanced materials, such as polymers and coatings, providing improved durability and performance in various applications.
  • Bioconjugation: It is employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted therapies and diagnostics.
  • Environmental Chemistry: This chemical is also explored for its potential in environmental applications, such as the development of sensors for detecting pollutants, contributing to environmental monitoring efforts.

Citations