221123-48-4

Basic information

• Product Name: 3-(3-isopropyloxy-4-methoxyphenyl)propanol-1
• Synonyms: 3-(3-isopropyloxy-4-methoxyphenyl)propanol-1
• CAS NO: 221123-48-4
• Molecular Weight: 224.3
• Mol File: 221123-48-4.mol

Chemical Properties

• CAS DataBase Reference: 3-(3-isopropyloxy-4-methoxyphenyl)propanol-1(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3-isopropyloxy-4-methoxyphenyl)propanol-1(221123-48-4)
• EPA Substance Registry System: 3-(3-isopropyloxy-4-methoxyphenyl)propanol-1(221123-48-4)

Safety Data

• Hazardous Substances Data: 221123-48-4(Hazardous Substances Data)

Upstream product

• 129150-61-4 3-(3-hydroxy-4-methoxyphenyl)-propionic acid methyl ester 

Downstream Products

• 1026879-23-1 methanesulfonic acid 1-[2-(4-fluoro-3-nitro-phenyl)-ethyl]-5-(3-isopropoxy-4-methoxy-phenyl)-pentyl ester 
• 221123-63-3 1-(4-fluoro-3-nitrophenyl)-7-(3-isopropoxy-4-methoxyphenyl)-3-iodoheptane 
• 221123-62-2 1-(4-fluoro-3-nitrophenyl)-7-(3-isopropoxy-4-methoxyphenyl)heptanol-3 
• 197382-79-9 1-(4-fluoro-3-nitro-phenyl)-7-(3-isopropoxy-4-methoxy-phenyl)-heptan-3-one 
• 221123-64-4 1-(4-fluoro-3-nitrophenyl)-7-(3-isopropoxy-4-methoxyphenyl)heptane 
• 221123-61-1 5-[7-(4-fluoro-3-nitrophenyl)-5-hydroxyheptyl]-2-methoxyphenol 
• 221123-65-5 5-[7-(4-fluoro-3-nitrophenyl)heptyl]-2-methoxyphenol 
• 197382-99-3 aceroside IV perbenzoate 
• 197382-92-6 2-(4-fluoro-3-nitrobenzyl)-7-(3-isopropoxy-4-methoxyphenyl)-3-oxoheptanoic acid methyl ester 
• 221123-52-0 1-(4-fluoro-3-nitrophenyl)-7-(3-hydroxy-4-methoxyphenyl)heptan-3-one 
• 221123-50-8 7-(3-isopropoxy-4-methoxyphenyl)-3-oxoheptanoic acid methyl ester 
• 221123-49-5 3-(3-isopropyloxy-4-methoxyphenyl)propyl iodide 

Relevant articles and documents

A unified strategy toward the synthesis of acerogenin-type macrocycles: Total syntheses of acerogenins A, B, C, and L and aceroside IV

A general strategy for the synthesis of acerogenin-type diarylheptanoids containing an endocyclic biaryl ether bond has been developed, and convergent total syntheses of acerogenin A, B, C, and L and aceroside IV have been accomplished. Cycloetherificatio