tert-butyl N-[3-[3-(trifluoromethyl)diazirin-3-yl]phenyl]carbamate

≥95%

Reagent Code: #216194
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CAS Number 1645279-82-8

science Other reagents with same CAS 1645279-82-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Formula C₁₃H₁₄F₃N₃O₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used in photoaffinity labeling studies to probe protein-ligand interactions. Upon exposure to light, the diazirine group generates a reactive carbene species that forms covalent bonds with nearby biomolecules, enabling the identification and mapping of binding sites in complex biological systems. The trifluoromethyl group enhances stability and increases lipophilicity, improving membrane permeability for use in live-cell labeling. The tert-butyl carbamate (Boc) group acts as a protecting group, allowing for controlled deprotection in synthetic sequences. Commonly applied in chemical biology and drug discovery to study protein-protein interactions and validate target engagement of small molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿4,180.00
1g
10-20 days ฿12,240.00
tert-butyl N-[3-[3-(trifluoromethyl)diazirin-3-yl]phenyl]carbamate
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Used in photoaffinity labeling studies to probe protein-ligand interactions. Upon exposure to light, the diazirine group generates a reactive carbene species that forms covalent bonds with nearby biomolecules, enabling the identification and mapping of binding sites in complex biological systems. The trifluoromethyl group enhances stability and increases lipophilicity, improving membrane permeability for use in live-cell labeling. The tert-butyl carbamate (Boc) group acts as a protecting group, allowing

Used in photoaffinity labeling studies to probe protein-ligand interactions. Upon exposure to light, the diazirine group generates a reactive carbene species that forms covalent bonds with nearby biomolecules, enabling the identification and mapping of binding sites in complex biological systems. The trifluoromethyl group enhances stability and increases lipophilicity, improving membrane permeability for use in live-cell labeling. The tert-butyl carbamate (Boc) group acts as a protecting group, allowing for controlled deprotection in synthetic sequences. Commonly applied in chemical biology and drug discovery to study protein-protein interactions and validate target engagement of small molecules.

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