40025-43-2

Basic information

• Product Name: 2-(4-Methoxyphenyl)-5-pentylfuran
• Synonyms: 2-(4-Methoxyphenyl)-5-pentylfuran
• CAS NO: 40025-43-2
• Molecular Weight: 244.334
• Mol File: 40025-43-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(4-Methoxyphenyl)-5-pentylfuran(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-Methoxyphenyl)-5-pentylfuran(40025-43-2)
• EPA Substance Registry System: 2-(4-Methoxyphenyl)-5-pentylfuran(40025-43-2)

Safety Data

• Hazardous Substances Data: 40025-43-2(Hazardous Substances Data)

Upstream product

• 3777-69-3 2-pentylfuran 
• 696-62-8 para-iodoanisole 
• 136022-06-5 1-(Methylsulfinyl)octa-1,2-diene 
• 818-72-4 1-Octyn-3-ol 
• 79802-21-4 oct-1-yn-3-yl 4-methylbenzenesulfonate 
• 136022-15-6 4-Methoxy-α-<1-(methylsulfinyl)oct-2-ynyl>benzenemethanol 

Relevant articles and documents

Direct arylation of heteroarenes catalyzed by a palladium-1,10- phenanthroline complex

A new entry in direct arylation of heteroarenes using Pd(OAc)2 and 1,10-phenanthroline as a nitrogen-based ligand is reported. The long induction period observed at the initial stage of the reaction was effectively reduced by modification of th

Substituted propargylic sulfoxides: synthesis and -sigmatropic rearrangement in the presence of thiophilic reagents

The allenic sulfoxides 2 and 12 were converted into the substituted propargylic sulfoxides 3 and 13, respectively, by deprotonation with methyl lithium and reaction with electrophilic reagents.Smooth thermal -sigmatropic rearrangement of 3 and 13, using 2-mercapto-1-methylimidazole to desulfurize the intermediate allenic sulfenate XVa, yielded the corresponding conjugated enones 10.The possible reaction mechanism for these two transformations were examined. Key words: Allenic sulfoxides; propargylic sulfoxides; organolithium compounds adjacent to sulfoxides; -sigmatropic rearrangement; desulfurization; α,β-unsaturated enones; furanes.