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Catalog Number:
39684
CAS Number:
87736-88-7
Alcool 4-[3-(trifluorométhyl)-3 H -diazirin-3-yl]benzylique
Purity:
≥ 97 % (HPLC)
Synonym(s):
3-[4-(hydroxyméthyl)phényl]-3-(trifluorométhyl)-3 H -diazirine
Documents
$105.56 /200 mg
Taille
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Informations sur le produit

4-[3-(Trifluoromethyl)-3H-diazirin-3-yl]benzyl alcohol is a versatile compound with significant applications in the fields of medicinal chemistry and materials science. This compound features a unique trifluoromethyl group, which enhances its reactivity and stability, making it an ideal candidate for various chemical transformations. Researchers utilize this compound in photochemistry and as a photoaffinity labeling agent, allowing for the study of protein interactions and drug-target engagements. Its diazirine moiety is particularly valuable in bioconjugation techniques, enabling the covalent attachment of biomolecules to surfaces or other molecules, which is crucial in the development of targeted therapies and diagnostic tools.

In addition to its applications in research, 4-[3-(Trifluoromethyl)-3H-diazirin-3-yl]benzyl alcohol is also explored for its potential in the synthesis of advanced materials, including polymers and nanomaterials. Its unique properties allow for the creation of functional materials with tailored characteristics, making it a valuable asset in the development of innovative solutions across various industries. With its combination of reactivity and stability, this compound stands out as a key player in advancing both scientific research and industrial applications.

Numéro CAS 
87736-88-7
Formule moléculaire
C9H7F3N2O
Poids moléculaire 
216.16
Indice de réfraction 
n20D 1.48
Informations générales
Numéro CAS 
87736-88-7
Formule moléculaire
C9H7F3N2O
Poids moléculaire 
216.16
Indice de réfraction 
n20D 1.48
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]benzyl alcohol is widely utilized in research focused on:

  • Photochemistry: This compound is valuable in photochemical studies due to its ability to undergo photolysis, making it useful for investigating light-induced chemical reactions.
  • Drug Development: It serves as a potential precursor in the synthesis of pharmaceuticals, particularly in creating targeted therapies that require precise molecular modifications.
  • Bioconjugation: The unique structure allows for efficient labeling and tracking of biomolecules, aiding in the development of diagnostic tools and therapeutic agents in the biomedical field.
  • Material Science: Its properties make it suitable for developing advanced materials, such as polymers with enhanced thermal and chemical resistance, which are crucial in various industrial applications.
  • Environmental Research: The compound can be used in studies related to environmental monitoring, particularly in assessing the degradation of pollutants under UV light exposure.

Citations