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6105-74-4

1,1-DIMETHYL-2-PIPERIDIN-1-YL-ETHYLAMINE

Catalog#: AR00EAU2  |   CAS#: 6105-74-4  |   MDL#: MFCD05022423  |   MF: C9H20N2  |   MW: 156.2685

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Catalog Number AR00EAU2
Chemical Name 1,1-DIMETHYL-2-PIPERIDIN-1-YL-ETHYLAMINE
CAS Number 6105-74-4
Molecular Formula C9H20N2
Molecular Weight 156.2685
MDL Number MFCD05022423
SMILES CC(CN1CCCCC1)(N)C

2-Methyl-1-(piperidin-1-yl)propan-2-amine, also known as $name$, is a versatile compound commonly utilized in chemical synthesis for its unique properties and capabilities. In the realm of organic chemistry, this compound plays a crucial role as a building block for the synthesis of various complex molecules and pharmaceuticals. Its specific structure, containing a piperidine ring and an amine group, allows for a range of synthetic transformations and functional group manipulations.One key application of 2-Methyl-1-(piperidin-1-yl)propan-2-amine is its use as a chiral amine intermediate in the synthesis of enantiomerically pure compounds. By incorporating this compound into a synthetic route, chemists can introduce chirality in a controlled manner, leading to the production of valuable chiral molecules with high optical purity. This is particularly important in the pharmaceutical industry, where enantiomeric purity often determines the biological activity and safety profile of a drug.Furthermore, 2-Methyl-1-(piperidin-1-yl)propan-2-amine can serve as a key component in the preparation of heterocyclic compounds, which are prevalent in medicinal chemistry and materials science. Its piperidine moiety can participate in various ring-forming reactions, enabling the construction of diverse ring systems with tailored properties and functionalities. This versatility makes it an indispensable tool for chemists seeking to access complex molecular architectures efficiently.In summary, 2-Methyl-1-(piperidin-1-yl)propan-2-amine is a crucial building block in chemical synthesis, offering a wide array of applications in the creation of chiral molecules, heterocyclic compounds, and pharmaceutical intermediates. Its strategic placement within synthetic pathways facilitates the preparation of intricate structures, making it a valuable asset for organic chemists striving to unlock new possibilities in molecular design and drug discovery.
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GHS Pictogram N/A
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