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N3-TFBA-O2Oc is a photochemical probe comprising azide and aryl groups. This type of azidoaryl compound serves as a classical precursor to nitro compounds and has been utilized by Fleet et al as a versatile photophore for probing biological receptors. Specifically, N3-TFBA-O2Oc functions as a photo-crosslinker (λmax=258 nm) in studies involving estrogen receptors and for direct surface coating of carbon and organic polymers. Additionally, as a click chemistry reagent, N3-TFBA-O2Oc contains an azide group that reacts with molecules featuring an alkyne group through a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc). It can also engage in strain-promoted azide-alkyne cycloaddition reactions (SPAAC) with molecules that possess DBCO or BCN groups.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | N3-TFBA-O2Oc is a photochemical probe comprising azide and aryl groups. This type of azidoaryl compound serves as a classical precursor to nitro compounds and has been utilized by Fleet et al as a versatile photophore for probing biological receptors. Specifically, N3-TFBA-O2Oc functions as a photo-crosslinker (λmax=258 nm) in studies involving estrogen receptors and for direct surface coating of carbon and organic polymers. Additionally, as a click chemistry reagent, N3-TFBA-O2Oc contains an azide group that reacts with molecules featuring an alkyne group through a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc). It can also engage in strain-promoted azide-alkyne cycloaddition reactions (SPAAC) with molecules that possess DBCO or BCN groups. |
| Molecular Weight | 380.25 |
| Formula | C13H12F4N4O5 |
| Cas No. | 1993119-45-1 |
| Smiles | [N-]=[N+]=NC1=C(F)C(F)=C(C(=O)NCCOCCOCC(=O)O)C(F)=C1F |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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