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7471-07-0

4-(2-Methylbut-3-Yn-2-Yl)Morpholine

Catalog#: AR008PYK  |   CAS#: 7471-07-0  |   MDL#: MFCD25966879  |   MF: C9H15NO  |   MW: 153.2215

Packsize Purity Price Availability Quantity
100mg 98% $107.00 Global Stock Buy Now Add To Cart
250mg 98% $153.00 Global Stock Buy Now Add To Cart
1g 98% $391.00 Global Stock Buy Now Add To Cart
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Catalog Number AR008PYK
Chemical Name 4-(2-Methylbut-3-Yn-2-Yl)Morpholine
CAS Number 7471-07-0
Molecular Formula C9H15NO
Molecular Weight 153.2215
MDL Number MFCD25966879
SMILES C#CC(N1CCOCC1)(C)C
NSC Number 403540

4-(1,1-Dimethylprop-2-ynyl)morpholine, also known by its chemical formula C9H15NO, is a versatile compound widely used in chemical synthesis applications. This specific morpholine derivative plays a crucial role in organic chemistry as a synthetic building block due to its unique structural properties and reactivity. Its incorporation into various chemical reactions enables the formation of complex molecular structures and the synthesis of valuable compounds across different industries.One of the key applications of 4-(1,1-Dimethylprop-2-ynyl)morpholine in chemical synthesis is its utilization as a ligand in transition-metal-catalyzed reactions. Due to the presence of the morpholine ring and the attached propargyl group, this compound can act as a bidentate ligand, coordinating with metal centers to facilitate catalytic processes. The resulting metal-ligand complex enhances the selectivity and efficiency of various catalytic reactions, such as cross-coupling reactions, hydrogenation, and carbonylation.Moreover, 4-(1,1-Dimethylprop-2-ynyl)morpholine serves as a valuable intermediate in the synthesis of biologically active molecules and pharmaceutical compounds. By incorporating this morpholine derivative into the molecular framework, chemists can introduce specific functional groups and stereochemical elements, ultimately leading to the production of novel drug candidates and therapeutic agents. Additionally, the propargyl functionality offers opportunities for further derivatization, allowing for the modification of the compound's properties and expanding its potential applications in drug discovery and development.In summary, the strategic incorporation of 4-(1,1-Dimethylprop-2-ynyl)morpholine in chemical synthesis enables the efficient construction of complex molecules, the enhancement of catalytic processes, and the synthesis of biologically relevant compounds with diverse applications in the pharmaceutical, agrochemical, and materials science sectors.
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