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Catalog Number:
40023
CAS Number:
24388-23-6
2-Phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, Phenylboronic acid pinacol ester
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Product Information

2-Phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile organoboron compound known for its unique structural properties and reactivity. This compound serves as a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its ability to participate in various coupling reactions, such as Suzuki-Miyaura cross-coupling, makes it an essential reagent for researchers looking to create complex molecular architectures. The presence of the boron atom enhances its utility in forming carbon-boron bonds, which are crucial in many synthetic pathways.

Additionally, 2-Phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane exhibits excellent stability and solubility in organic solvents, making it easy to handle and integrate into various reaction conditions. Its unique properties allow for selective reactions, which can lead to higher yields and purities in synthetic processes. This compound is particularly beneficial for chemists focused on developing innovative materials and pharmaceuticals, providing a reliable option for efficient synthesis and functionalization.

Synonyms
(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, Phenylboronic acid pinacol ester
CAS Number
24388-23-6
Purity
≥ 98% (GC)
Molecular Formula
C12H17BO2
Molecular Weight
204.08
MDL Number
MFCD00966985
PubChem ID
570673
Melting Point
28 °C (Lit.)
Appearance
White to off-white powder to lump
Boiling Point
130 °C / 20 mmHg (Lit.)
Conditions
Store at RT
General Information
Synonyms
(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, Phenylboronic acid pinacol ester
CAS Number
24388-23-6
Purity
≥ 98% (GC)
Molecular Formula
C12H17BO2
Molecular Weight
204.08
MDL Number
MFCD00966985
PubChem ID
570673
Melting Point
28 °C (Lit.)
Appearance
White to off-white powder to lump
Boiling Point
130 °C / 20 mmHg (Lit.)
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-Phenyl-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 molecules, making it invaluable for researchers developing new pharmaceuticals.
  • Cross-Coupling Reactions: It plays a crucial role in cross-coupling reactions, such as Suzuki reactions, allowing for the formation of carbon-carbon bonds, which is essential in the development of advanced materials and agrochemicals.
  • Fluorescent Probes: The compound is used in the creation of fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes and understanding disease mechanisms.
  • Polymer Chemistry: It is utilized in polymerization processes to enhance the properties of polymers, leading to materials with improved durability and performance in various applications, including packaging and coatings.
  • Environmental Chemistry: This chemical is also explored for its potential in environmental applications, such as the development of sensors for detecting pollutants, contributing to efforts in environmental monitoring and protection.

Citations