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

Catalog Number:
40011
CAS Number:
269410-26-6
4,4,5,5-tétraméthyl-2-(4-phénoxyphényl)-1,3,2-dioxaborolane
Purity:
≥ 98% (CG)
Synonym(s):
4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)phénoxybenzène, Ester pinacol de l'acide phénoxyphényl-4-boronique
Documents
$39.56 /1G
Taille
Request Bulk Quote
Product Information

4,4,5,5-Tetramethyl-2-(4-phenoxyphenyl)-1,3,2-dioxaborolane is a versatile boron-containing compound known for its unique properties and applications in organic synthesis and materials science. This compound serves as an effective reagent in various chemical reactions, particularly in the formation of carbon-carbon bonds, making it invaluable for researchers in the fields of medicinal chemistry and polymer development. Its ability to facilitate cross-coupling reactions enhances its utility in the synthesis of complex organic molecules, which is crucial for drug discovery and development.

Additionally, 4,4,5,5-Tetramethyl-2-(4-phenoxyphenyl)-1,3,2-dioxaborolane exhibits excellent stability and solubility in organic solvents, allowing for easy handling and incorporation into various reaction conditions. Its unique structure provides a platform for further functionalization, enabling the design of tailored compounds for specific applications. This compound is particularly beneficial for professionals seeking efficient and reliable reagents for their synthetic pathways, offering a competitive edge in research and industrial applications.

Synonyms
4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)phénoxybenzène, Ester pinacol de l'acide phénoxyphényl-4-boronique
CAS Number
269410-26-6
Purity
≥ 98% (CG)
Molecular Formula
C 18 H 21 BO 3
Molecular Weight
296.17
MDL Number
MFCD06795691
PubChem ID
17750275
Melting Point
52 - 56 °C
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Magasin chez RT
General Information
Synonyms
4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)phénoxybenzène, Ester pinacol de l'acide phénoxyphényl-4-boronique
CAS Number
269410-26-6
Purity
≥ 98% (CG)
Molecular Formula
C 18 H 21 BO 3
Molecular Weight
296.17
MDL Number
MFCD06795691
PubChem ID
17750275
Melting Point
52 - 56 °C
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

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

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, facilitating the formation of complex molecules through cross-coupling reactions, which are essential in the development of pharmaceuticals and agrochemicals.
  • Material Science: It is used in the synthesis of advanced materials, particularly in the creation of polymers and coatings that exhibit improved thermal and mechanical properties, making them suitable for high-performance applications.
  • Medicinal Chemistry: The compound plays a crucial role in drug discovery, particularly in the development of targeted therapies, by acting as a building block for biologically active molecules.
  • Fluorescent Probes: It is employed in the design of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high specificity and sensitivity.
  • Environmental Applications: The compound is also explored for its potential in environmental remediation, particularly in the development of sensors for detecting pollutants, thus contributing to sustainability efforts.

Citations