Azides

Azides

Azides are highly versatile nitrogen-rich reagents used extensively in organic synthesis, pharmaceuticals, materials science, and click chemistry. Their unique –N? functional group enables participation in cycloaddition reactions, particularly the CuAAC “click” reaction, forming triazoles with exceptional efficiency and selectivity. Azides also serve as precursors for amines, nitrenes, and heterocycles through reduction, rearrangement, and insertion reactions. In polymer and surface chemistry, azides enable photo-crosslinking, surface modification, and macromolecular conjugation. Their thermal and energetic properties make certain azides useful in propellants and detonators, though controlled handling is essential. With broad functional-group compatibility and high reactivity, azides remain indispensable tools in modern synthetic and chemical biology applications.

tert-Butyl 3-(Azidomethyl)Piperidine-1-Carboxylate(Saltdata: Free) CAS NO 162167-94-4

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CAS No.:162167-94-4

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Content:99.90%

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(S)-Ethyl 2-Azido-2-Phenylethanoate CAS NO 162402-58-6

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CAS No.:162402-58-6

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Fmoc-Photo-Linker CAS NO 162827-98-7

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CAS No.:162827-98-7

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2(1H)-Pyridinethione, 1-(2-Azidoethyl)- CAS NO 162970-31-2

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CAS No.:162970-31-2

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Benzoic Acid, 3,5-Diazido- CAS NO 162993-50-2

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CAS No.:162993-50-2

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Fmoc-4-Azido-L-Phenylalanine CAS NO 163217-43-4

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CAS No.:163217-43-4

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Methyl-2,3,4-Tri-o-Acetyl-Beta-D-Galactopyranosyluronosyl Azide CAS NO 163776-36-1

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CAS No.:163776-36-1

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S-[2-(4-Azidosalicylamido)Ethylthio]-2-Thiopyridine CAS NO 164575-82-0

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CAS No.:164575-82-0

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