CAS 92992-92-2
:N-(5-chloropyridin-2-yl)ethane-1,2-diamine
Description:
N-(5-chloropyridin-2-yl)ethane-1,2-diamine is an organic compound characterized by its structure, which includes a pyridine ring substituted with a chlorine atom and an ethane backbone featuring two amine groups. This compound typically appears as a solid or liquid, depending on its purity and environmental conditions. It is soluble in polar solvents, such as water and alcohols, due to the presence of the amine functional groups, which can engage in hydrogen bonding. The chlorine substituent on the pyridine ring can influence the compound's reactivity and biological activity, making it of interest in medicinal chemistry and drug development. The presence of the amine groups suggests potential applications in the synthesis of various derivatives or as a ligand in coordination chemistry. Additionally, the compound may exhibit specific pharmacological properties, which would require further investigation through biological assays. Safety data should be consulted, as compounds with amine functionalities can be hazardous, and appropriate handling procedures should be followed.
Formula:C7H10ClN3
InChI:InChI=1/C7H10ClN3/c8-6-1-2-7(11-5-6)10-4-3-9/h1-2,5H,3-4,9H2,(H,10,11)
SMILES:c1cc(=NCCN)[nH]cc1Cl
Synonyms:- 2-(2-Aminoethylamino)-5-chloropyridine
- 92992-92-2
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