Aminopyridine
Aminopyridine refers to a group of organic compounds where an amino group (-NH2) is attached to a pyridine ring, which is a six-membered aromatic ring containing five carbon atoms and one nitrogen atom. The position of the amino group on the ring defines the specific isomer, with the most common being 2-aminopyridine, 3-aminopyridine, and 4-aminopyridine, each having unique chemical and physical properties. These compounds are significant in the pharmaceutical and agrochemical industries, often serving as key intermediates in the synthesis of drugs, pesticides, and other fine chemicals. Aminopyridines are valued for their reactivity, particularly in substitution and coupling reactions, and their ability to form hydrogen bonds, which can influence their solubility, stability, and biological activity.
- Structure
- Product name
- CAS No.
- Molecular formula
- Inquiry
![(3-Chlorophenyl)-(1H-pyrazolo[4,3-b]pyridin-3-yl)aMine](http://file1.lookchem.com/300w/synthetic/2022-02-06-11/8311e80d-e36d-4d2d-a10c-b26a3e9c8556.png)
![5-[4-(1-Methylethoxy)phenyl]-2-pyridinamine](http://file1.lookchem.com/300w/substances/2022-02-26-07/dd114ffd-aa4d-467e-b7c8-2ec84e5a4256.png)
![Thiazolo[5,4-c]pyridin-2-amine](http://file1.lookchem.com/300w/substances/2022-03-04-04/03a62a9f-fbe5-4c2b-bbc5-07c9e89b8e31.png)
![Oxazolo[4,5-c]pyridin-2-amine (9CI)](http://www.lookchem.com/300w/2010/073/114498-55-4.jpg)
![Thiazolo[4,5-b]pyridin-2-amine](http://file1.lookchem.com/cas/reactions/2021/08/27/637793.png)
