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Catalog Number:
39679
CAS Number:
1258874-29-1
Chlorhydrate de 4-[3-(trifluorométhyl)-3 H -diazirin-3-yl]benzylamine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Chlorhydrate de 3-[4-(aminométhyl)phényl]-3-(trifluorométhyl)-3 H -diazirine
Documents
$232.25 /200 mg
Taille
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Informations sur le produit

4-[3-(Trifluoromethyl)-3H-diazirin-3-yl]benzylamine hydrochloride is a specialized compound known for its unique properties and applications in various fields, particularly in chemical biology and medicinal chemistry. This compound features a trifluoromethyl group, which enhances its reactivity and stability, making it an ideal candidate for use in photoaffinity labeling experiments. Researchers can utilize this compound to study protein interactions and cellular processes, providing valuable insights into biological mechanisms. Its ability to form covalent bonds upon UV irradiation allows for precise targeting of biomolecules, facilitating advancements in drug discovery and development.

In addition to its applications in research, 4-[3-(Trifluoromethyl)-3H-diazirin-3-yl]benzylamine hydrochloride can be employed in the synthesis of novel pharmaceuticals and agrochemicals. The trifluoromethyl group imparts unique electronic properties, which can enhance the biological activity of derived compounds. This makes it a valuable tool for chemists looking to innovate and optimize new chemical entities. With its distinctive features and versatile applications, this compound stands out as a significant resource for professionals in the chemical and pharmaceutical industries.

Numéro CAS 
1258874-29-1
Formule moléculaire
C9H8F3N3 · HCl
Poids moléculaire 
251.64
Point de fusion 
142 °C (déc.)
Informations générales
Numéro CAS 
1258874-29-1
Formule moléculaire
C9H8F3N3 · HCl
Poids moléculaire 
251.64
Point de fusion 
142 °C (déc.)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

4-[3-(Trifluoromethyl)-3H-diazirin-3-yl]benzylamine hydrochloride is widely utilized in research focused on:

  • Photocrosslinking Studies: This compound is effective in biological research for photocrosslinking proteins and nucleic acids, allowing scientists to study interactions and structures under specific light conditions.
  • Drug Development: Its unique trifluoromethyl group enhances the compound's stability and bioavailability, making it a valuable candidate in the design of new pharmaceuticals.
  • Imaging Techniques: Used in advanced imaging methods, it helps in tracing biological pathways and understanding cellular processes, which is crucial in both academic and clinical research.
  • Material Science: The compound can be incorporated into polymers to create materials with specific properties, such as increased resistance to heat and chemicals, beneficial in various industrial applications.
  • Environmental Monitoring: Its ability to form stable complexes with certain pollutants makes it useful in developing sensors for detecting environmental contaminants, aiding in pollution control efforts.

Citations