(1R,2S,5S)—6,6-DiMethyl-3-aza-bicylo[3.1.0]hexane-2-carboxylic acid Methyl ester hydrochloride CAS: 565456-77-1
Catalog Number | XD93398 |
Product Name | (1R,2S,5S)—6,6-DiMethyl-3-aza-bicylo[3.1.0]hexane-2-carboxylic acid Methyl ester hydrochloride |
CAS | 565456-77-1 |
Molecular Formula | C9H16ClNO2 |
Molecular Weight | 205.68 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
(1R,2S,5S)—6,6-DiMethyl-3-aza-bicylo[3.1.0]hexane-2-carboxylic acid Methyl ester hydrochloride is a chemical compound with various applications in pharmaceutical research and drug development.One of the key uses of this compound is as a chiral building block in the synthesis of pharmaceutical intermediates and active pharmaceutical ingredients (APIs). Its unique bicyclic structure and chirality make it valuable in the production of enantiomerically pure compounds. By incorporating this compound into the synthesis, chemists can control the stereochemistry and create specific pharmacological properties in the resulting molecules. This is particularly important in drug development, where the desired biological activity often depends on the spatial arrangement of the molecule.Additionally, (1R,2S,5S)—6,6-DiMethyl-3-aza-bicylo[3.1.0]hexane-2-carboxylic acid Methyl ester hydrochloride is used as a precursor for the synthesis of quinuclidine-based drugs. Quinuclidine derivatives have shown a wide range of biological activities, including antipsychotic, anticonvulsant, and analgesic properties. By introducing specific functional groups to the compound, chemists can modify its pharmacokinetic and pharmacodynamic properties, enhancing its therapeutic potential.Furthermore, this compound finds use as a reactant or catalyst in organic transformations. Due to the presence of a tertiary amine and the sterically hindered nature of the methyl groups, it can participate in various chemical reactions, such as amidation, alkylation, and cycloaddition reactions. Its reactivity and ability to form complex intermediates make it a versatile tool in organic synthesis, allowing for the creation of structurally diverse compounds.In summary, (1R,2S,5S)—6,6-DiMethyl-3-aza-bicylo[3.1.0]hexane-2-carboxylic acid Methyl ester hydrochloride is a valuable compound in drug development and organic synthesis. Its chirality and unique structure enable the production of enantiomerically pure compounds and the synthesis of quinuclidine-based drugs with specific pharmacological properties. Its reactivity also makes it a useful reactant and catalyst in various chemical transformations. Overall, this compound plays a significant role in the advancement of pharmaceutical research and the development of new therapeutic agents.