141-86-6
141-86-6
Chemical Structure
2,6-Diaminopyridine
- CAS No.: 141-86-6
- Formula:C5H7N3
- Molecular Weight:109.13
IUPAC Name: pyridine-2,6-diamine
InChIKey: VHNQIURBCCNWDN-UHFFFAOYSA-N
SMILES: NC1=NC(N)=CC=C1
Biological Activity: 2,6-Diaminopyridine is an intermediate and coupling agent for hair dyes. 2,6-Diaminopyridine participates in organic synthesis reactions such as N-methylation and can bind metal ions by forming macrocyclic ligands through condensation with aldehydes. 2,6-Diaminopyridine can be used to synthesize the analgesic phenazopyridine hydrochloride (HY-B0985)[1][2].
| Cat. No. | Nom du produit | Pureté | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
2,6-Diaminopyridine | 99.96% | 2,6-Diaminopyridine is an intermediate and coupling agent for hair dyes. 2,6-Diaminopyridine participates in organic synthesis reactions such as N-methylation and can bind metal ions by forming macrocyclic ligands through condensation with aldehydes. 2,6-Diaminopyridine can be used to synthesize the analgesic phenazopyridine hydrochloride (HY-B0985). | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2,6-Diaminopyridine (Standard) | ≥98% | 2,6-Diaminopyridine (Standard) is the analytical standard of 2,6-Diaminopyridine (HY-Y0198). This product is intended for research and analytical applications. 2,6-Diaminopyridine is an intermediate and coupling agent for hair dyes. 2,6-Diaminopyridine participates in organic synthesis reactions such as N-methylation and can bind metal ions by forming macrocyclic ligands through condensation with aldehydes. 2,6-Diaminopyridine can be used to synthesize the analgesic phenazopyridine hydrochloride (HY-B0985). | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Ilhan S, et al. Synthesis, characterization and redox properties of macrocyclic Schiff base by reaction of 2, 6-diaminopyridine and 1, 3-bis (2-carboxyaldehyde phenoxy) propane and its CuII, NiII, PbII, CoIII and LaIII complexes. Transition Metal Chemistry, 2007, 32(3): 344-349.
- [2]. Nabati M, et al. One-pot and one-step novel N-methylation of 2, 6-diaminopyridine[J]. Iranian chemical communication, 2014, 2(3, pp. 162-231, Serial No. 4): 162-167.
