logo
Home  > 3-(Methylamino)tetrahydropyran

AE16835

120811-33-8 | 3-(Methylamino)tetrahydropyran

Packsize Purity Availability Price Discounted Price    Quantity
50mg 95% 1 week $313.00 $219.00 -   +
100mg 95% 1 week $424.00 $297.00 -   +
250mg 95% 1 week $571.00 $400.00 -   +
500mg 95% 1 week $849.00 $595.00 -   +
1g 95% 1 week $1,067.00 $747.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE16835
Chemical Name: 3-(Methylamino)tetrahydropyran
CAS Number: 120811-33-8
Molecular Formula: C6H13NO
Molecular Weight: 115.1735
MDL Number: MFCD09037816
SMILES: CNC1CCCOC1

 

Upstream Synthesis Route
  • N-Methyltetrahydro-2H-pyran-3-amine, also known as $name$, is a versatile compound widely used in chemical synthesis processes. Its unique molecular structure allows it to participate in various reactions, making it a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.One key application of N-Methyltetrahydro-2H-pyran-3-amine is as a precursor in the synthesis of heterocyclic compounds. Its presence in the starting material enables the formation of complex ring structures through cyclization reactions, providing a convenient route to diverse molecular scaffolds. This makes it an essential component in the development of novel compounds with potential biological activities.Furthermore, N-Methyltetrahydro-2H-pyran-3-amine can also serve as a chiral auxiliary in asymmetric synthesis. Its stereochemical properties allow for the creation of enantiomerically pure molecules, which is crucial in the production of pharmaceuticals and other high-value compounds. By leveraging the chiral nature of this compound, chemists can efficiently access enantiomerically enriched products with high levels of selectivity.Overall, the application of N-Methyltetrahydro-2H-pyran-3-amine in chemical synthesis showcases its versatility and importance in the production of complex molecules. Its role as a building block and chiral auxiliary highlights its value in the design and development of new chemical entities with diverse applications.
FEATURED PRODUCTS