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Catalog Number:
39936
CAS Number:
874363-18-5
N- [3-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)phényl]acrylamide
Purity:
≥ 97% (RMN)
Synonym(s):
Ester pinacol de l'acide 3-acrylamidophénylboronique, 2-(3-acrylamidophényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
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Product Information

N-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acrylamide is a versatile compound with significant applications in organic synthesis and materials science. This compound features a unique boron-containing moiety that enhances its reactivity and stability, making it an ideal candidate for use in cross-coupling reactions and as a building block in the development of advanced polymers. Its ability to form stable complexes with various substrates allows researchers to explore innovative pathways in drug discovery and materials development.

In the pharmaceutical industry, N-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acrylamide can be utilized in the synthesis of bioactive compounds, contributing to the creation of new therapeutic agents. Additionally, its properties make it suitable for applications in sensor technology and nanotechnology, where precision and stability are paramount. Researchers and industry professionals will find this compound particularly beneficial for developing high-performance materials and conducting advanced chemical research.

Synonyms
Ester pinacol de l'acide 3-acrylamidophénylboronique, 2-(3-acrylamidophényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
CAS Number
874363-18-5
Purity
≥ 97% (RMN)
Molecular Formula
C 15 H 20 BNO 3
Molecular Weight
273.14
MDL Number
MFCD22493996
PubChem ID
74789486
Melting Point
160 - 165 ?C
Appearance
Blanc cassé uni
Conditions
Magasin chez RT
General Information
Synonyms
Ester pinacol de l'acide 3-acrylamidophénylboronique, 2-(3-acrylamidophényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
CAS Number
874363-18-5
Purity
≥ 97% (RMN)
Molecular Formula
C 15 H 20 BNO 3
Molecular Weight
273.14
MDL Number
MFCD22493996
PubChem ID
74789486
Melting Point
160 - 165 ?C
Appearance
Blanc cassé uni
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

N-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acrylamide is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, aiding chemists in developing new pharmaceuticals and agrochemicals.
  • Polymer Chemistry: It is used in the formulation of specialty polymers, enhancing material properties such as flexibility and thermal stability, which are crucial in manufacturing high-performance materials.
  • Bioconjugation: The chemical's unique structure allows for effective bioconjugation techniques, facilitating the development of targeted drug delivery systems in biomedical research.
  • Fluorescent Probes: This compound can be utilized in creating fluorescent probes for biological imaging, providing researchers with tools to visualize cellular processes in real-time.
  • Environmental Applications: It plays a role in the development of sensors for detecting environmental pollutants, contributing to efforts in environmental monitoring and protection.

Citations