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Catalog Number:
39944
CAS Number:
171364-79-7
4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)anisole
Purity:
≥ 98% (CG)
Synonym(s):
Ester pinacol de l'acide 4-méthoxyphénylboronique, 2-(4-méthoxyphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
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Product Information

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anisole is a versatile compound widely utilized in organic synthesis and materials science. This boron-containing compound is particularly valued for its role in Suzuki-Miyaura cross-coupling reactions, which are essential for the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its unique structure, featuring a dioxaborolane moiety, enhances its reactivity and stability, making it an excellent choice for researchers looking to develop new pharmaceuticals, agrochemicals, or advanced materials.

In addition to its synthetic applications, this compound can also serve as a building block in the development of functional materials, such as OLEDs (organic light-emitting diodes) and other electronic devices. Its ability to facilitate efficient charge transport and its compatibility with various substrates make it a valuable asset in the field of organic electronics. Researchers and industry professionals can leverage the unique properties of 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anisole to drive innovation and enhance the performance of their products.

Synonyms
Ester pinacol de l'acide 4-méthoxyphénylboronique, 2-(4-méthoxyphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
CAS Number
171364-79-7
Purity
≥ 98% (CG)
Molecular Formula
C 13 H 19 BO 3
Molecular Weight
234.1
MDL Number
MFCD05663864
PubChem ID
584319
Density
1,04 g/mL
Appearance
Poudre blanche à blanc cassé en grumeaux
Refractive Index
n20D = 1,51
Conditions
Magasin chez RT
General Information
Synonyms
Ester pinacol de l'acide 4-méthoxyphénylboronique, 2-(4-méthoxyphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
CAS Number
171364-79-7
Purity
≥ 98% (CG)
Molecular Formula
C 13 H 19 BO 3
Molecular Weight
234.1
MDL Number
MFCD05663864
PubChem ID
584319
Density
1,04 g/mL
Appearance
Poudre blanche à blanc cassé en grumeaux
Refractive Index
n20D = 1,51
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anisole is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, enabling the creation of complex molecules through cross-coupling reactions.
  • Pharmaceutical Development: It plays a crucial role in the synthesis of pharmaceutical intermediates, aiding in the development of new drugs with enhanced efficacy and reduced side effects.
  • Material Science: The compound is used in the formulation of advanced materials, such as polymers and coatings, that require specific chemical properties for improved performance.
  • Bioconjugation: It is applied in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Fluorescent Probes: This chemical is utilized in the development of fluorescent probes for imaging applications, providing researchers with tools for studying biological processes in real-time.

Citations