Benzenemethanol, 3-ethynyl-5-[3-(trifluoromethyl)-3H-diazirin-3-yl]-

Reagent Code: #142334
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CAS Number 849607-27-8

science Other reagents with same CAS 849607-27-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.18 g/mol
Formula C₁₁H₇F₃N₂O
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a photoaffinity labeling agent in biochemical and pharmacological research. Its diazirine group generates highly reactive carbenes upon UV light exposure, enabling covalent binding to nearby biomolecules such as proteins or nucleic acids. The ethynyl group allows for downstream conjugation via click chemistry, facilitating detection, isolation, or enrichment of labeled targets. This compound is especially valuable in studying protein-ligand interactions, mapping binding sites, and identifying unknown receptors in complex biological systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿23,750.00

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Benzenemethanol, 3-ethynyl-5-[3-(trifluoromethyl)-3H-diazirin-3-yl]-
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Used primarily as a photoaffinity labeling agent in biochemical and pharmacological research. Its diazirine group generates highly reactive carbenes upon UV light exposure, enabling covalent binding to nearby biomolecules such as proteins or nucleic acids. The ethynyl group allows for downstream conjugation via click chemistry, facilitating detection, isolation, or enrichment of labeled targets. This compound is especially valuable in studying protein-ligand interactions, mapping binding sites, and ident

Used primarily as a photoaffinity labeling agent in biochemical and pharmacological research. Its diazirine group generates highly reactive carbenes upon UV light exposure, enabling covalent binding to nearby biomolecules such as proteins or nucleic acids. The ethynyl group allows for downstream conjugation via click chemistry, facilitating detection, isolation, or enrichment of labeled targets. This compound is especially valuable in studying protein-ligand interactions, mapping binding sites, and identifying unknown receptors in complex biological systems.

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