From Surf Wiki (app.surf) — the open knowledge base
3-Aminopyridine
3-Aminopyridine is an aminopyridine. It is a colorless solid.
Preparation
3-Aminopyridine is prepared by heating nicotinamide with sodium hypobromite (Hofmann rearrangement), which is in turn prepared in situ by the reaction of sodium hydroxide and bromine at 70 °C.
:[[File:Synthesis of 3-Aminopyridine.gif]]
It can be used in the synthesis of organic ligand 3-pyridylnicotinamide. Troxipide is another synthesis that uses 3-AP.
Toxicity
The acute toxicity is indicated by the = 178 mg/kg (quail, oral).
References
References
- (1950). "3-Aminopyridine".
- (2000). "Pyridine and Pyridine Derivatives".
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
Ask Mako anything about 3-Aminopyridine — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report