CAS 925890-81-9
:N-(4-bromoisoquinolin-1-yl)ethane-1,2-diamine
Description:
N-(4-bromoisoquinolin-1-yl)ethane-1,2-diamine is a chemical compound characterized by its unique structure, which includes an isoquinoline moiety substituted with a bromine atom and an ethane-1,2-diamine functional group. This compound typically exhibits properties associated with both aromatic and aliphatic amines, such as potential solubility in polar solvents and the ability to participate in hydrogen bonding due to the presence of amino groups. The bromine substitution can influence its reactivity, making it a candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the isoquinoline structure may impart biological activity, making it of interest in medicinal chemistry for potential therapeutic applications. The compound's molecular weight, melting point, and specific reactivity would depend on its precise formulation and purity. As with many amines, it may also exhibit basicity, allowing it to interact with acids to form salts. Safety and handling precautions should be observed due to the presence of bromine and the potential for biological activity.
Formula:C11H12BrN3
InChI:InChI=1/C11H12BrN3/c12-10-7-15-11(14-6-5-13)9-4-2-1-3-8(9)10/h1-4,7H,5-6,13H2,(H,14,15)
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Found 1 products.
1-(2-Aminoethyl)amino-4-bromoisoquinoline
CAS:<p>1-(2-Aminoethyl)amino-4-bromoisoquinoline</p>Purity:≥95%Molecular weight:266.13707g/mol
