| Chemical Name: | 1-[(2-methylpropan-2-yl)oxycarbonyl]-3-oxopiperidine-4-carboxylic acid |
| CAS Number: | 936497-91-5 |
| Product Number: | AG00H2W3(AGN-PC-08XZXH) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C11H17NO5 |
| Molecular Weight: | 243.2564 |
1-(tert-Butoxycarbonyl)-3-oxopiperidine-4-carboxylic acid, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis as a key building block. This compound serves as a crucial intermediate in the preparation of various pharmaceuticals, agrochemicals, and functional materials.In chemical synthesis, $name$ is frequently used as a protecting group for amines due to its stability and ease of removal under mild conditions. By selectively blocking the amino group with the tert-butoxycarbonyl (Boc) moiety, unwanted side reactions can be minimized during the synthesis of complex molecules. This protection strategy allows chemists to manipulate other functional groups in the molecule without affecting the amine functionality.Furthermore, the presence of the 3-oxo and carboxylic acid groups in $name$ offers additional synthetic pathways for introducing various functionalities into the final molecule. These functional groups can undergo a wide range of chemical transformations, including condensation reactions, esterifications, and nucleophilic additions, enabling the incorporation of diverse structural motifs in the target compound.Overall, the strategic incorporation of 1-(tert-Butoxycarbonyl)-3-oxopiperidine-4-carboxylic acid in chemical synthesis not only facilitates the construction of complex molecules but also provides chemists with a valuable tool for controlling reactivity and selectivity in organic reactions.
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