424788-79-4

Basic information

• Product Name: Methanesulfonic acid, trifluoro-, 2-formyl-4-methoxyphenyl ester
• CAS NO: 424788-79-4
• Molecular Formula: C9H7F3O5S
• Molecular Weight: 284.213
• Mol File: 424788-79-4.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Methanesulfonic acid, trifluoro-, 2-formyl-4-methoxyphenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Methanesulfonic acid, trifluoro-, 2-formyl-4-methoxyphenyl ester(424788-79-4)
• EPA Substance Registry System: Methanesulfonic acid, trifluoro-, 2-formyl-4-methoxyphenyl ester(424788-79-4)

Safety Data

• Hazardous Substances Data: 424788-79-4(Hazardous Substances Data)

Upstream product

• 672-13-9 2-hydroxy-5-methoxybenzaldehyde 
• 358-23-6 trifluoromethylsulfonic anhydride 
• 37595-74-7 N,N-phenylbistrifluoromethane-sulfonimide 

Downstream Products

• 1309881-72-8 2-(5-methoxy-2-{3-[(2-methylallyl)(toluene-4-sulfonyl)amino]prop-1-ynyl}benzyl)-3-oxobutyric acid ethyl ester 
• 1309881-90-0 C₂₂H₂₅NO₄S 
• 1132669-90-9 5-methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde 
• 223553-44-4 2-(2-phenylethenyl)-5-methoxybenzaldehyde 

Relevant articles and documents

CYCLOPROPYL ETHYLENE COMPOUND AND ARTHROPOD PEST CONTROL COMPOSITION CONTAINING SAME

The present invention provides a compound that have excellent harmful arthropod controlling effects, the compounds being represented by formula (I) [wherein R1 represents a hydrogen atom etc., and R21, R22, R31

Construction of spirofused tricyclic frameworks by NHC-catalyzed intramolecular stetter reaction of a benzaldehyde tether with a cyclic exsnone

Various benzaldehyde tethers with a cyclic enone were prepared from commercially available 2-hydroxybenzaldehydes via a three-step sequence involving triflate formation, Sonogashira cross-coupling, and regioselective hydrogenation. These substrates were t

Pd(II)-catalyzed one-pot, three-step route for the synthesis of unsymmetrical acridines

Unsymmetric acridines are synthesized via a one-pot amination/cyclization/ aromatization reaction for the first time. With Pd(OAc)2-X-Phos as the catalyst, a series of unsymmetric acridines are obtained in moderate to excellent yields (up to 99