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Catalog Number:
39925
CAS Number:
475250-57-8
4,4,5,5-tétraméthyl-2-(naphtalène-1-ylméthyl)-1,3,2-dioxaborolane
Purity:
≥ 93% (CG)
Synonym(s):
Ester pinacol de l'acide (naphtalène-1-ylméthyl)boronique, 1-[(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)méthyl]naphtalène
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Product Information

4,4,5,5-Tetramethyl-2-(naphthalen-1-ylmethyl)-1,3,2-dioxaborolane is a versatile boron-containing compound that has garnered attention in organic synthesis and materials science. This compound is particularly valued for its role as a reagent in cross-coupling reactions, which are essential for forming carbon-carbon bonds in the synthesis of complex organic molecules. Its unique structure allows for enhanced reactivity and selectivity, making it an ideal choice for researchers looking to streamline their synthetic pathways.

In addition to its applications in organic synthesis, this dioxaborolane derivative has potential uses in the development of advanced materials, including organic light-emitting diodes (OLEDs) and other electronic devices. The compound's stability and compatibility with various substrates make it a promising candidate for researchers aiming to innovate in the fields of electronics and photonics. With its ability to facilitate efficient reactions and contribute to the creation of high-performance materials, 4,4,5,5-Tetramethyl-2-(naphthalen-1-ylmethyl)-1,3,2-dioxaborolane stands out as a valuable asset in both academic and industrial settings.

Synonyms
Ester pinacol de l'acide (naphtalène-1-ylméthyl)boronique, 1-[(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)méthyl]naphtalène
CAS Number
475250-57-8
Purity
≥ 93% (CG)
Molecular Formula
C 17 H 21 BO 2
Molecular Weight
268.16
MDL Number
MFCD22419278
PubChem ID
11254165
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Ester pinacol de l'acide (naphtalène-1-ylméthyl)boronique, 1-[(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)méthyl]naphtalène
CAS Number
475250-57-8
Purity
≥ 93% (CG)
Molecular Formula
C 17 H 21 BO 2
Molecular Weight
268.16
MDL Number
MFCD22419278
PubChem ID
11254165
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4,4,5,5-Tetramethyl-2-(naphthalen-1-ylmethyl)-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 carbon-carbon bonds. Its unique structure allows for efficient coupling reactions, making it invaluable for synthesizing complex organic molecules.
  • Pharmaceutical Development: In the pharmaceutical industry, it is used to create novel drug candidates. Its ability to modify biological molecules can lead to the development of more effective medications with improved bioavailability.
  • Materials Science: The compound is employed in the production of advanced materials, particularly in the development of polymers and nanomaterials. Its properties enhance the performance and stability of these materials, making them suitable for high-tech applications.
  • Fluorescent Probes: It is utilized in the design of fluorescent probes for biological imaging. These probes can help researchers visualize cellular processes in real-time, providing insights into disease mechanisms and treatment effects.
  • Environmental Applications: The compound has potential uses in environmental chemistry, such as in the detection and removal of pollutants. Its reactivity can be harnessed to develop methods for monitoring and mitigating environmental contaminants.

Citations