Chemical Name: | Bicyclo[3.2.1]octane-1,5-dicarboxylic acid, monomethyl ester |
CAS Number: | 110371-27-2 |
Product Number: | AG0093QH(AGN-PC-0NXD5B) |
Synonyms: | |
MDL No: | |
Molecular Formula: | C11H15O4- |
Molecular Weight: | 211.2344 |
5-(Methoxycarbonyl)bicyclo[3.2.1]octane-1-carboxylic acid, also known as $name$, is a versatile compound commonly utilized in chemical synthesis for its unique structural properties and reactivity. In chemical synthesis, this compound serves as a key building block for the preparation of various complex molecules due to its ability to undergo diverse reactions and form important intermediates. $name$ is particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals where its bicyclic structure plays a crucial role in the formation of intricate molecular frameworks. Its methoxycarbonyl group serves as a protecting group that can be selectively removed under specific conditions, allowing for further functionalization and manipulation of the molecule. Additionally, the carboxylic acid functionality in $name$ provides opportunities for conjugation, cross-coupling reactions, and derivatization, enabling the creation of novel compounds with tailored properties. Furthermore, the strained bicyclo[3.2.1]octane ring system of $name$ imparts unique steric and electronic effects that influence the outcome of chemical reactions, making it a valuable tool in the hands of synthetic chemists seeking to access challenging chemical space. Whether used in complex natural product synthesis or in the design of new materials, 5-(Methoxycarbonyl)bicyclo[3.2.1]octane-1-carboxylic acid exhibits great potential for facilitating innovative and efficient synthetic pathways.