36895-36-0

Basic information

• Product Name: 7-((3-phenylisoxazol-5-yl)methoxy)-4-methyl-2H-benzopyran-2-one
• Synonyms: 7-((3-phenylisoxazol-5-yl)methoxy)-4-methyl-2H-benzopyran-2-one
• CAS NO: 36895-36-0
• Molecular Weight: 333.343
• Mol File: 36895-36-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 7-((3-phenylisoxazol-5-yl)methoxy)-4-methyl-2H-benzopyran-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-((3-phenylisoxazol-5-yl)methoxy)-4-methyl-2H-benzopyran-2-one(36895-36-0)
• EPA Substance Registry System: 7-((3-phenylisoxazol-5-yl)methoxy)-4-methyl-2H-benzopyran-2-one(36895-36-0)

Safety Data

• Hazardous Substances Data: 36895-36-0(Hazardous Substances Data)

Upstream product

• 36895-28-0 4-methyl-7-((3-phenyl-4,5-dihydroisoxazol-5-yl)methoxy)-2Hchromen-2-one 
• 3993-57-5 7-allyloxy-4-methyl-2H-chromen-2-one 
• 90924-12-2 3-phenyl-5-hydroxymethylisoxazole 
• 932-90-1 Benzaldoxime 
• 100-52-7 benzaldehyde 
• 108-46-3 recorcinol 
• 2039-50-1 5-bromomethyl-3-phenyl-isoxazole 
• 67268-43-3 7-propargyloxy-4-methyl-2H-chromen-2-one 
• 698-16-8 benzohydroximoyl chloride 
• 90-33-5 7-hydroxy-4-methyl-chromen-2-one 
• 873-67-6 benzonitrile oxide 

Relevant articles and documents

Coumarin phenyl isoxazole derivatives and applications thereof

The invention relates to coumarin phenyl isoxazole derivatives and applications thereof. 4'-hydroxyl chalcone is taken as the raw materials. 4'-hydroxyl chalcone reacts with bromomethyl isoxazole with different substituent groups in the presence of potass

Design and synthesis of antimicrobial, anticoagulant, and anticholinesterase hybrid molecules from 4-methylumbelliferone

We designed and synthesized new series of diverse triazoles, isoxazoles, isoxazolines, and aziridines linked 4-methylumbelliferone 1 using intermolecular 1,3-dipolar cycloaddition reactions. Structures of these compounds were established on the basis of 1H NMR, 13C NMR, and ESI-HRMS. All prepared compounds were evaluated for their antimicrobial, anticoagulant, and anticholinesterase activities. Interestingly, among the tested molecules, some of the analogs displayed better activities than the parent 4-methylumbelliferone 1 such as 6a and 6d for their antifungal properties. Moreover, compounds 4, 5, 6, and 7 showed the importance of the added fragments to 4-methylumbelliferone 1 via the linker methylene to have good activity.