(1R,2S,5S)—6,6-DiMethyl-3-aza-bicylo[3.1.0]hexane-2-carboxylic acid Methyl ester hydrochloride CAS:565456-77-1

The compound has three stereocenters, denoted by the (1R,2S,5S) configuration, which determines the three-dimensional orientation of the atoms within the molecule. This chirality is important for the molecule's biological activity and its interactions with other molecules. The 6,6-dimethyl substituents on the larger ring enhance the steric hindrance, which can influence the compound's chemical reactivity and its ability to engage in hydrogen bonding. The presence of the methyl ester group provides a point of esterification, which can be used to attach additional functional groups or to modify the molecule's physicochemical properties. The carboxylic acid moiety is fully protonated in the hydrochloride salt form, increasing the compound's overall charge and potentially enhancing its solubility in aqueous media. The hydrochloride form is often used for handling and storage due to its increased stability. The compound's complexity and the presence of various functional groups make it a challenging target for synthesis but also provide opportunities for its use in the制备 of more complex molecules. Its potential applications include medicinal chemistry, where it could serve as a building block for the synthesis of drugs, or in the field of organic chemistry, where it could be used in the construction of more elaborate molecular architectures.