23203-48-7

Basic information

• Product Name: 4-methyl-4-(p-methoxyphenyl)pentanoic acid
• Synonyms: 4-methyl-4-(p-methoxyphenyl)pentanoic acid
• CAS NO: 23203-48-7
• Molecular Weight: 222.284
• Mol File: 23203-48-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-methyl-4-(p-methoxyphenyl)pentanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-4-(p-methoxyphenyl)pentanoic acid(23203-48-7)
• EPA Substance Registry System: 4-methyl-4-(p-methoxyphenyl)pentanoic acid(23203-48-7)

Safety Data

• Hazardous Substances Data: 23203-48-7(Hazardous Substances Data)

Upstream product

• 23203-47-6 4-methyl-4-p-hydroxyphenyl-1-pentanoic acid 
• 77-78-1 dimethyl sulfate 
• 108-95-2 phenol 
• 33214-54-9 3-p-Anisyl-3-methyl-1-butanol 
• 1663-39-4 tert-Butyl acrylate 
• 100-66-3 methoxybenzene 
• 690-94-8 dimethyl(vinylethynyl)carbinol 
• 819-44-3 5-chloro-5-methyl-1-hexen-3-yne 
• 504-85-8 4-methyl-pent-3-enoic acid 
• 124-38-9 carbon dioxide 
• 33214-40-3 1-Brom-3-p-anisyl-3-methylbutan 
• 860548-14-7 4-(4-methoxy-phenyl)-4-methyl-pent-2-ynoic acid 
• 23203-46-5 4-(p-Aminophenyl)-4-methylvaleriansaeure 
• 2696-33-5 4-<1,1-Dimethyl-penten-(4)-in-(2)-yl>-phenol 

Downstream Products

• 23203-51-2 6-methoxy-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one 
• 29510-28-9 4-(p-Anisyl-4-methylpent-1-yl)-p-brombenzolsulfonat 
• 54877-73-5 4-methyl-4-(4-oxocyclohexenyl)pentanoic acid 
• 23203-49-8 7-methoxy-4,4-dimethyl-3,4-dihydronaphthalen-1(2H)-one 
• 26315-95-7 4-Methyl-4-p-methoxyphenyl-1-pentanol 
• 77658-64-1 methyl 4-methyl-4-(4-oxocyclohexenyl)pentanoate 

Relevant articles and documents

A heavy-metal-free desulfonylative Giese-type reaction of benzothiazole sulfones under visible-light conditions

A visible-light-induced desulfonylative Giese-type reaction has been developed. Essential to the success is the employment of Hantzsch ester to activate benzothiazole sulfones without any heavy-metal additives. Not only benzylic benzothiazole sulfones but also alkyl ones were viable substrates and reacted with electron-deficient alkenes and a propiol amide.