73087-65-7

Basic information

• Product Name: 1-(4-methoxyphenyl)-4-(3-methoxyphenyl)butan-1-ol
• Synonyms: 1-(4-methoxyphenyl)-4-(3-methoxyphenyl)butan-1-ol
• CAS NO: 73087-65-7
• Molecular Weight: 286.371
• Mol File: 73087-65-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(4-methoxyphenyl)-4-(3-methoxyphenyl)butan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methoxyphenyl)-4-(3-methoxyphenyl)butan-1-ol(73087-65-7)
• EPA Substance Registry System: 1-(4-methoxyphenyl)-4-(3-methoxyphenyl)butan-1-ol(73087-65-7)

Safety Data

• Hazardous Substances Data: 73087-65-7(Hazardous Substances Data)

Upstream product

• 74973-35-6 (4-Methoxy-phenyl)-[2-(3-methoxy-phenyl)-cyclopropyl]-methanone 
• 57668-35-6 3-[3-(Benzyloxy)phenyl]-1-propanol 
• 75849-10-4 ethyl 3-<3-(benzyloxy)phenyl>propanoate 
• 1971-83-1 3-(3-bromopropyl)phenol 
• 6943-97-1 (m-methoxyphenyl)propyl bromide 
• 123-11-5 4-methoxy-benzaldehyde 
• 78074-34-7 4-(3-Methoxy-phenyl)-1-(4-methoxy-phenyl)-butan-1-one 

Downstream Products

• 73087-67-9 6-methoxy-1-(4-methoxyphenyl)-1,2,3,4-tetrahydronaphthalene 
• 73087-66-8 8-methoxy-1-(4-methoxyphenyl)-1,2,3,4-tetrahydronaphthalene 

Relevant articles and documents

Reductive Cleavage of Arylcyclopropyl Ketones

Arylcyclopropyl aryl ketones undergo clean but slow reductive cleavage to 4-arylbutyrophenones when heated with zinc in ethanol.Replacement of one the aryl groups by an alkyl group strongly inhibits reaction.This effect is in part overcome by the use of a higher boiling alcohol.When substituted at the cyclopropyl methylene position by an ethoxycarbonyl group these cyclopropyl ketones also undergo cleavage but with the unexpected formation of the ethyl 3,5-diaryl-5-oxopentanoates (22).In general, the results are consistent with the formation of an anion-radical intermediate.