N-(2-(2-(2-Aminoethoxy)ethoxy)ethyl)-4-(3-(trifluoromethyl)-3H-diazirin-3-yl)benzamide

96%

Reagent Code: #219893
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CAS Number 655224-73-0

science Other reagents with same CAS 655224-73-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 360.33 g/mol
Formula C₁₅H₁₉F₃N₄O₃
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in biochemical and biophysical research for photoaffinity labeling, enabling the study of protein-ligand interactions. Upon exposure to light, the diazirine group generates reactive carbenes that form covalent bonds with nearby biomolecules, helping to capture and identify transient molecular interactions. The trifluoromethyl group enhances photochemical stability and labeling efficiency. The polyether linker provides flexibility and improved solubility, facilitating access to binding sites in complex biological systems. Commonly applied in mapping drug-binding sites, receptor-ligand interactions, and protein-protein interfaces.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿56,680.00
inventory 250mg
10-20 days ฿84,210.00
N-(2-(2-(2-Aminoethoxy)ethoxy)ethyl)-4-(3-(trifluoromethyl)-3H-diazirin-3-yl)benzamide
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Used in biochemical and biophysical research for photoaffinity labeling, enabling the study of protein-ligand interactions. Upon exposure to light, the diazirine group generates reactive carbenes that form covalent bonds with nearby biomolecules, helping to capture and identify transient molecular interactions. The trifluoromethyl group enhances photochemical stability and labeling efficiency. The polyether linker provides flexibility and improved solubility, facilitating access to binding sites in compl

Used in biochemical and biophysical research for photoaffinity labeling, enabling the study of protein-ligand interactions. Upon exposure to light, the diazirine group generates reactive carbenes that form covalent bonds with nearby biomolecules, helping to capture and identify transient molecular interactions. The trifluoromethyl group enhances photochemical stability and labeling efficiency. The polyether linker provides flexibility and improved solubility, facilitating access to binding sites in complex biological systems. Commonly applied in mapping drug-binding sites, receptor-ligand interactions, and protein-protein interfaces.

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