157790-73-3

Basic information

• Product Name: Methanesulfonic acid, trifluoro-, 5-formyl-2-methoxyphenyl ester
• CAS NO: 157790-73-3
• Molecular Formula: C9H7F3O5S
• Molecular Weight: 284.213
• Mol File: 157790-73-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Methanesulfonic acid, trifluoro-, 5-formyl-2-methoxyphenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Methanesulfonic acid, trifluoro-, 5-formyl-2-methoxyphenyl ester(157790-73-3)
• EPA Substance Registry System: Methanesulfonic acid, trifluoro-, 5-formyl-2-methoxyphenyl ester(157790-73-3)

Safety Data

• Hazardous Substances Data: 157790-73-3(Hazardous Substances Data)

Upstream product

• 4885-02-3 Dichloromethyl methyl ether 
• 59099-58-0 2-methoxyphenyl triflate 
• 621-59-0 isovanillin 
• 17763-80-3 para-nitrophenyl triflate 
• 358-23-6 trifluoromethylsulfonic anhydride 

Downstream Products

• 4383-06-6 3-hydroxy-4-methoxybenzyl alcohol 
• 443776-91-8 [4-methoxy-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanol 
• 31825-29-3 3‐isopropyl‐4‐methoxybenzaldehyde 
• 160625-54-7 4-methoxy-3-(3-methyl-3-buten-1-ynyl)acetophenone 
• 160625-53-6 1-<4-methoxy-3-(3-methyl-3-buten-1-ynyl)phenyl>ethanol 
• 160625-49-0 3-ethynyl-4-methoxybenzaldehyde 
• 121007-15-6 4-methoxy-3-(3'-methylbut-3'-en-1'-ynyl)benzyl alcohol 
• 121007-18-9 4-methoxy-3-(3'-methylbut-3'-en-1'-ynyl)benzaldehyde 
• 10035-16-2 benzofuran-5-carbaldehyde 
• 3015-20-1 dehydrotremetone 
• 31823-05-9 5-hydroxymethylbenzo[b]furan 
• 160625-48-9 4-methoxy-3-[2-(trimethylsilyl)ethynyl]benzaldehyde 
• 160625-50-3 4-methoxy-3-(3-hydroxy-3-methyl-1-butynyl)benzaldehyde 
• 38493-59-3 (3-bromo-4-methoxy-phenyl)-methanol 

Relevant articles and documents

4-Nitrophenyltriflate and 4-Nitrophenylnonaflate as New Perfluoroalkanesulfonyl Transfer Agents: Experimental and Computational Studies

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Directed ortho Metalation (D o M)-Linked Corriu-Kumada, Negishi, and Suzuki-Miyaura Cross-Coupling Protocols: A Comparative Study

A systematic study of the widely used, titled name reaction transition-metal-catalyzed cross-coupling reactions with attention to context with the directed ortho metalation (D o M) is reported. In general, the Suzuki-Miyaura and Negishi protocols show gre

The conversion of phenols to the corresponding aryl halides under mild conditions

Mild, novel procedures have been developed for the syntheses of aryl halides from the corresponding phenols in modest to good yields via boronate ester intermediates.