53557-95-2

Basic information

• Product Name: Isoxazole, 5-[2-(4-methoxyphenyl)ethenyl]-3-methyl-4-nitro-
• CAS NO: 53557-95-2
• Molecular Formula: C13H12N2O4
• Molecular Weight: 260.249
• Mol File: 53557-95-2.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Isoxazole, 5-[2-(4-methoxyphenyl)ethenyl]-3-methyl-4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Isoxazole, 5-[2-(4-methoxyphenyl)ethenyl]-3-methyl-4-nitro-(53557-95-2)
• EPA Substance Registry System: Isoxazole, 5-[2-(4-methoxyphenyl)ethenyl]-3-methyl-4-nitro-(53557-95-2)

Safety Data

• Hazardous Substances Data: 53557-95-2(Hazardous Substances Data)

Upstream product

• 123-54-6 acetylacetone 
• 300-87-8 3,5-dimethyl-1,2-oxazole 
• 1123-49-5 3,5-dimethyl-4-nitroisoxazole 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 103806-30-0 2-Acetyl-3-(4-methoxy-phenyl)-4-(3-methyl-4-nitro-isoxazol-5-yl)-butyric acid ethyl ester 
• 79510-61-5 3-[1-(4-Methoxy-phenyl)-2-(3-methyl-4-nitro-isoxazol-5-yl)-ethyl]-pentane-2,4-dione 
• 754985-40-5 4-amino-3-methyl-5-[(E)-2-(4-methoxyphenyl)-1-ethenyl]isoxazole 
• 1021951-87-0 (1R,2S)-1-(4-methoxyphenyl)-2-(3-methyl-4-nitro-isoxazol-5-yl)-ethane-1,2-diol 
• 53558-02-4 5-(4-methoxy-styryl)-3-methyl-isoxazol-4-ylamine 
• 1205553-70-3 (S)-5-(2-(4-methoxyphenyl)-3-nitropropyl)-3-methyl-4-nitroisoxazole 
• 1205553-75-8 (R)-5-(2-(4-methoxyphenyl)-3-nitropropyl)-3-methyl-4-nitroisoxazole 
• 1229422-27-8 1-(4-methoxyphenyl)-2-(3-methyl-4-nitroisoxazol-5-yl)ethanesulfonic acid 
• 1334145-76-4 (S)-5-(2-(4-methoxyphenyl)-2-(phenylthio)ethyl)-3-methyl-4-nitroisoxazole 
• 1371645-01-0 (+)-dimethyl 2-(4-methoxyphenyl)-3-(3-methyl-4-nitroisoxazol-5-yl)cyclopropane-1,1-dicarboxylate 
• 1380544-27-3 5-(4-methoxyphenethyl)-3-methyl-4-nitroisoxazole 

Relevant articles and documents

Phosphine-Catalyzed [3 + 2] Annulation of Morita-Baylis-Hillman Carbonates with Isoxazole-Based Alkenes

A phosphine-catalyzed [3 + 2] annulation of Morita-Baylis-Hillman (MBH) carbonates with 3-methyl-4-nitro-5-styrylisoxazoles has been developed to afford various multifunctional isoxazoles in moderate to good yields with moderate to excellent diastereoselectivities. With a spirocyclic chiral phosphine as the catalyst, up to 89% ee was obtained.

An efficient solvent-free synthesis of 3-methyl-4-nitro-5-styrylisoxazoles using solid nano-titania

Abstract: An efficient and solvent-free procedure for the synthesis of 3-methyl-4-nitro-5-styrylisoxazoles using nano-titania as solid support and recyclable catalyst is presented. This method provides clean, simple, solvent-free and useful alternative to

One-pot synthesis of functionalized isoxazole-thiolane hybrids via Knoevenagel condensation and domino sulfa-1,6-Michael/intramolecular vinylogous Henry reactions

One-pot synthesis of highly functionalized tetrahydrothiophene (thiolane) derivatives conjugated with biologically useful isooxazole are reported via the Knoevenagel condensation followed by domino sulfa-1,6-Michael/intramolecular vinylogous Henry reactio