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Catalog Number:
46039
CAS Number:
73899-14-6
3-Fenil-3-(trifluorometil) -3H- diazirina
Purity:
≥ 98 % (HPLC)
Documents
$50.00 /25 mg
Tamaño
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Product Information

3-Phenyl-3-(trifluoromethyl)-3H-diazirine is a versatile chemical compound known for its unique reactivity and applications in various fields, particularly in organic synthesis and materials science. This diazirine derivative features a trifluoromethyl group, which enhances its stability and reactivity, making it an excellent candidate for photochemical studies and as a labeling agent in biological research. Its ability to form covalent bonds upon exposure to UV light allows researchers to track molecular interactions and dynamics in complex biological systems, providing valuable insights into cellular processes.

In addition to its applications in biological research, 3-Phenyl-3-(trifluoromethyl)-3H-diazirine is also utilized in the development of advanced materials, including polymers and coatings. Its unique properties enable the modification of surfaces and the creation of functionalized materials with tailored characteristics. This compound stands out in comparison to similar diazirine derivatives due to its trifluoromethyl substitution, which imparts enhanced chemical stability and reactivity, making it a preferred choice for researchers and industry professionals seeking reliable and effective solutions for their projects.

CAS Number
73899-14-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C8H5F3N2
Molecular Weight
186.14
MDL Number
MFCD22041649
PubChem ID
11116743
Appearance
Líquido transparente de color amarillo claro a amarillo a naranja.
Refractive Index
n20D 1,44
Conditions
Conservar entre 2 y 8 °C.
General Information
CAS Number
73899-14-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C8H5F3N2
Molecular Weight
186.14
MDL Number
MFCD22041649
PubChem ID
11116743
Appearance
Líquido transparente de color amarillo claro a amarillo a naranja.
Refractive Index
n20D 1,44
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Phenyl-3-(trifluoromethyl)-3H-diazirine is widely utilized in research focused on:

  • Photoaffinity Labeling: This compound is used in biochemical studies to label proteins and other biomolecules upon exposure to light, allowing researchers to track interactions and binding sites effectively.
  • Drug Discovery: In pharmaceutical research, it aids in identifying potential drug targets by covalently attaching to specific proteins, helping to elucidate mechanisms of action for new therapeutics.
  • Material Science: It serves as a useful tool in the development of advanced materials, particularly in creating polymer networks that require precise cross-linking under UV light.
  • Environmental Chemistry: The compound is employed in studies assessing the behavior of pollutants, enabling scientists to understand how certain chemicals interact with biological systems in the environment.
  • Bioconjugation Techniques: It facilitates the attachment of biomolecules to surfaces or other molecules, enhancing the functionality of biosensors and diagnostic tools in medical applications.

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