CAS 92993-40-3
:N1-(5-Bromo-2-pyridinyl)-1,3-propanediamine
Description:
N1-(5-Bromo-2-pyridinyl)-1,3-propanediamine, with the CAS number 92993-40-3, is an organic compound characterized by its structure, which includes a propanediamine backbone substituted with a 5-bromo-2-pyridinyl group. This compound typically exhibits properties associated with both amines and heterocyclic aromatic compounds. It is likely to be a solid at room temperature, with potential solubility in polar solvents due to the presence of amine functional groups. The bromine substituent can influence its reactivity, making it a candidate for various chemical reactions, including nucleophilic substitutions. Additionally, the pyridine ring may impart unique electronic properties, affecting its interaction with biological systems or its utility in medicinal chemistry. The compound may also exhibit basicity due to the amine groups, which can participate in hydrogen bonding and coordination with metal ions. Overall, N1-(5-Bromo-2-pyridinyl)-1,3-propanediamine is of interest in research fields such as pharmaceuticals and materials science.
Formula:C8H12BrN3
InChI:InChI=1S/C8H12BrN3/c9-7-2-3-8(12-6-7)11-5-1-4-10/h2-3,6H,1,4-5,10H2,(H,11,12)
InChI key:InChIKey=CJPNRBHTHRCYQX-UHFFFAOYSA-N
SMILES:N(CCCN)C1=CC=C(Br)C=N1
Synonyms:- 1,3-Propanediamine, N-(5-bromo-2-pyridinyl)-
- 1,3-Propanediamine, N< sup> 1< /sup> -(5-bromo-2-pyridinyl)-
- 2-(3-Aminopropylamino)-5-bromopyridine
- N<sup>1</sup>-(5-Bromo-2-pyridinyl)-1,3-propanediamine
- N<sup>1</sup>-(5-Bromopyridin-2-yl)propane-1,3-diamine
- N1-(5-Bromopyridin-2-yl)propane-1,3-diamine
- 1,3-Propanediamine, N1-(5-bromo-2-pyridinyl)-
- N1-(5-Bromo-2-pyridinyl)-1,3-propanediamine
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