1589493-42-4

Basic information

• Product Name: methyl (2E)-2-{[N-(2-formylphenyl)(4-methylbenzene)sulfonamido]methyl}-3-(4-fluorophenyl)prop-2-enoate
• Synonyms: methyl (2E)-2-{[N-(2-formylphenyl)(4-methylbenzene)sulfonamido]methyl}-3-(4-fluorophenyl)prop-2-enoate
• CAS NO: 1589493-42-4
• Molecular Weight: 467.518
• Mol File: 1589493-42-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: methyl (2E)-2-{[N-(2-formylphenyl)(4-methylbenzene)sulfonamido]methyl}-3-(4-fluorophenyl)prop-2-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (2E)-2-{[N-(2-formylphenyl)(4-methylbenzene)sulfonamido]methyl}-3-(4-fluorophenyl)prop-2-enoate(1589493-42-4)
• EPA Substance Registry System: methyl (2E)-2-{[N-(2-formylphenyl)(4-methylbenzene)sulfonamido]methyl}-3-(4-fluorophenyl)prop-2-enoate(1589493-42-4)

Safety Data

• Hazardous Substances Data: 1589493-42-4(Hazardous Substances Data)

Upstream product

• 5344-90-1 2-Aminobenzyl alcohol 
• 98-59-9 p-toluenesulfonyl chloride 
• 90312-02-0 N-(2-hydroxymethylphenyl)-4-methylbenzenesulfonamide 
• 353506-65-7 methyl 3-(4-fluorophenyl)-3-hydroxy-2-methylenepropanoate 
• 1010396-60-7 methyl (Z)-4-(bromomethyl)-3-(4-fluorophenyl)-2-propenoate 
• 6590-65-4 N-(2-Formyl-phenyl)-4-methyl-benzenesulfonamide 

Relevant articles and documents

Synthesis, crystal structure analysis, spectral investigations, DFT computations, Biological activities and molecular docking of methyl(2E)-2-{[N-(2-formylphenyl)(4-methylbenzene) sulfonamido]methyl}-3-(4-fluorophenyl)prop-2-enoate, a potential bioactive

The title compound methyl(2E)-2-{[N-(2-formylphenyl) (4-methylbenzene)sulfonamido]methyl}-3-(4-fluorophenyl) prop-2-enoate (MFMSF) has been synthesized and single crystals were grown by slow evaporation solution growth technique at room temperature. The g

Multicomponent cascade assembly for quinolinopyranpyrazole architectures

A highly efficient, multicomponent protocol for the construction of functionalized quinolinopyranpyrazole scaffolds with high stereoselectivity has been developed through the application of a domino reaction. All the quinolinopyranpyrazoles were synthesiz