| Chemical Name: | methyl 4-methylpiperidine-3-carboxylate,hydrochloride |
| CAS Number: | 908244-98-4 |
| Product Number: | AG00GXTR(AGN-PC-0WAJ5V) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C8H15NO2 |
| Molecular Weight: | 157.2102 |
Methyl 4-methylnipecotate is a versatile chemical compound widely utilized in chemical synthesis processes. As an ester derivative of nipecotic acid, it serves as a crucial building block in the development of various pharmaceuticals and organic compounds. Its application in chemical synthesis is particularly noteworthy in the pharmaceutical industry, where it is employed in the creation of novel drug molecules with diverse biological activities.One of the key uses of Methyl 4-methylnipecotate is in the synthesis of nipecotic acid analogs, which have demonstrated potential in the treatment of neurological disorders such as epilepsy. By incorporating this compound into the molecular structure of pharmaceutical agents, researchers can explore new pathways for drug discovery and therapeutic interventions. Additionally, Methyl 4-methylnipecotate plays a significant role in the formation of heterocyclic compounds, which are essential in medicinal chemistry for their biological activities and pharmaceutical applications.Moreover, this compound serves as a valuable intermediate in the preparation of complex organic molecules through various synthetic routes. Its chemical properties and reactivity enable chemists to modify the structure of organic compounds and enhance their desired properties, leading to the development of innovative materials and substances with diversified applications.In summary, Methyl 4-methylnipecotate is a key component in chemical synthesis, particularly in pharmaceutical research and development. Its versatility and significance in creating biologically active molecules make it an indispensable tool for chemists and researchers seeking to explore new frontiers in drug discovery and organic chemistry.
![O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]](https://img.angenechemical.com/storage/3a59/3a5932eec850ab245f6f4d4a7f9497f9.png)
(Cl)Cl)c1c(C)cc(cc1C)C](https://img.angenechemical.com/storage/6693/66939a3f08a27d2b6717c3194e00970b.png)
