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Catalog Number:
19664
CAS Number:
660431-65-2
[1-(2-Fluorophenyl)-1-tosyl]methyl isocyanide
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Product Information

[1-(2-Fluorophenyl)-1-tosyl]methyl isocyanide is a versatile compound with significant applications in organic synthesis and medicinal chemistry. Known for its unique reactivity, this isocyanide can be utilized in the construction of complex molecular architectures, making it an invaluable tool for researchers focused on drug discovery and development. Its ability to participate in various coupling reactions allows for the efficient formation of carbon-nitrogen bonds, which are crucial in the synthesis of pharmaceuticals and agrochemicals.

Moreover, the presence of the fluorophenyl and tosyl groups enhances its electrophilic character, providing additional pathways for functionalization. This compound has been employed in the synthesis of novel bioactive molecules, showcasing its potential in the development of new therapeutic agents. Its unique properties not only facilitate innovative research but also offer a competitive edge in the synthesis of compounds that may exhibit improved efficacy and selectivity in biological applications.

CAS Number
660431-65-2
Molecular Formula
C15H12FNO2S
Molecular Weight
289.33
MDL Number
MFCD04114778
PubChem ID
46738231
Conditions
Store at 0-8°C
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
General Information
CAS Number
660431-65-2
Molecular Formula
C15H12FNO2S
Molecular Weight
289.33
MDL Number
MFCD04114778
PubChem ID
46738231
Conditions
Store at 0-8°C
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Properties
Additional property information coming soon!
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Applications

[1-(2-Fluorophenyl)-1-tosyl]methyl isocyanide is widely utilized in research focused on:

  • Drug Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of novel anti-cancer agents.
  • Organic Synthesis: It is used in the preparation of complex organic molecules, enabling chemists to create diverse compounds with specific functional groups.
  • Material Science: The compound finds applications in the creation of advanced materials, including polymers and coatings, which exhibit enhanced properties such as durability and resistance to environmental factors.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems.
  • Analytical Chemistry: This isocyanide is utilized in various analytical methods, aiding researchers in the detection and quantification of specific compounds in complex mixtures.

Citations