Product Description
Cigna Qingdao is mainly engaged in the intermediates of febuxostatin, ceflothrin, eprazole, flubiprofen, phenalidone, tovaptan, rivaroxaban and Avanafil, terbinafine intermediates, thioacetamide and thiophene and their derivatives.
AI Product Description
*The following content is generated by AI and is for reference only.
4-(4-Aminophenyl)morpholin-3-one is a specialized organic compound belonging to the class of morpholine derivatives, characterized by a six-membered heterocyclic ring containing both oxygen and nitrogen atoms, fused with an amino-substituted phenyl group. Its molecular formula is C10H12N2O2, reflecting its composition of ten carbon atoms, twelve hydrogen atoms, two nitrogen atoms, and two oxygen atoms. While specific commercial Cas numbers may vary depending on the manufacturer or regional database updates, this compound is widely recognized in chemical literature for its structural utility in pharmaceutical research and agrochemical development. The presence of the primary amine group on the phenyl ring combined with the lactam functionality within the morpholine core offers versatile reactivity, making it an excellent intermediate for synthesizing complex bioactive molecules.
In the pharmaceutical industry, this molecule serves as a crucial building block for developing novel therapeutics targeting various diseases, including cancer, infectious diseases, and neurological disorders. Researchers utilize its unique scaffold to construct libraries of compounds aimed at optimizing drug potency and selectivity. The morpholinone moiety often enhances metabolic stability and solubility, key properties for oral bioavailability in drug candidates. Furthermore, due to its potential to interact with specific enzyme active sites, derivatives of 4-(4-Aminophenyl)morpholin-3-one are investigated for their ability to modulate biological pathways involved in cell proliferation and inflammation.
Beyond medicine, this compound finds applications in materials science, particularly in the synthesis of advanced polymers and functional dyes. The aromatic amine allows for easy modification through diazotization or coupling reactions, enabling the creation of chromophores with distinct optical properties. In agricultural chemistry, similar structures are explored for designing safer pesticides with reduced environmental impact. Overall, 4-(4-Aminophenyl)morpholin-3-one represents a significant tool in modern synthetic chemistry, bridging the gap between fundamental molecular design and practical industrial application. Its continued study supports innovation across multiple sectors, driving the development of next-generation solutions for global health and sustainability challenges.