6,6-diMethyl-3-azabicyclo[3.1.0]hexane (Hydrochloride) CAS:943516-55-0

The 6,6-dimethyl substituents on the larger ring enhance the steric hindrance, shielding the nitrogen atom and affecting the compound's reactivity. The presence of two methyl groups also increases the lipophilicity of the compound, which can influence its interaction with biological membranes and its potential as a drug candidate. The three-membered ring, known as an aziridine ring, is highly strained and can undergo ring-opening reactions under certain conditions, leading to the formation of new chemical species. This reactivity makes the compound a valuable precursor for the synthesis of more complex molecules. The hydrochloride salt form of 6,6-dimethyl-3-azabicyclo[3.1.0]hexane is often used in organic synthesis due to its improved handling and storage characteristics compared to the free base. The presence of the chloride ion can also influence the compound's solubility and reactivity in aqueous solutions. In summary, 6,6-dimethyl-3-azabicyclo[3.1.0]hexane hydrochloride is a versatile compound with applications in organic synthesis and medicinal chemistry. Its unique structure and the presence of functional groups make it a valuable starting material for the synthesis of a wide range of organic compounds, including those with potential therapeutic applications.