CAS 199522-66-2
:N1-(5-Bromopyrid-2-yl)ethane-1,2-diamine
Description:
N1-(5-Bromopyrid-2-yl)ethane-1,2-diamine, with the CAS number 199522-66-2, is an organic compound characterized by its structure, which includes a pyridine ring substituted with a bromine atom and an ethane-1,2-diamine moiety. This compound typically exhibits properties associated with both amines and halogenated aromatic compounds. It is likely to be a solid at room temperature, with potential solubility in polar solvents due to the presence of amine groups. The bromine substituent can influence its reactivity, making it a candidate for various chemical reactions, including nucleophilic substitutions. The presence of the amine groups suggests that it may engage in hydrogen bonding, affecting its physical properties such as melting and boiling points. Additionally, this compound may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activity often associated with pyridine derivatives. Safety data should be consulted for handling, as halogenated compounds can pose health risks.
Formula:C7H10BrN3
InChI:InChI=1/C7H10BrN3/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]cc1Br
Synonyms:- 199522-66-2
- N-(5-bromopyridin-2-yl)ethane-1,2-diamine
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Found 2 products.
1,2-Ethanediamine, N1-(5-bromo-2-pyridinyl)-
CAS:Formula:C7H10BrN3Purity:96%Color and Shape:SolidMolecular weight:216.0784N1-(5-Bromopyrid-2-yl)ethane-1,2-diamine
CAS:Formula:C7H10BrN3Purity:95.0%Color and Shape:Liquid, OilMolecular weight:216.082

