| Chemical Name: | 1-(3-Aminomethyl-piperidin-1-yl)-ethanone |
| CAS Number: | 915922-81-5 |
| Product Number: | AG00GVR2(AGN-PC-0WALB4) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C8H16N2O |
| Molecular Weight: | 156.2254 |
1-[3-(Aminomethyl)-1-piperidinyl]ethanone, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure consisting of a piperidine ring with an aminoethyl moiety positions it as a valuable intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, $name$ is utilized for its functional groups that can undergo a range of reactions, including reductive amination, nucleophilic substitution, and condensation reactions. The amino group in the piperidine ring allows for selective derivatization, facilitating the synthesis of diverse compounds with tailored properties.Additionally, the presence of the piperidine ring in $name$ provides the molecule with stereochemical properties that are advantageous in the creation of chiral compounds. This makes it an essential component in the preparation of enantiomerically pure substances, which are often crucial in the pharmaceutical industry for the development of drugs with specific biological activities.Furthermore, the incorporation of 1-[3-(Aminomethyl)-1-piperidinyl]ethanone into chemical synthesis pathways enables the efficient construction of complex molecular structures with high yields and selectivity. Its compatibility with various reaction conditions and compatibility with a wide range of functional groups make it a valuable tool for synthetic chemists striving to access novel compounds for various applications.
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