57596-01-7

Basic information

• Product Name: 4-(3-hydroxy-4-methoxyphenyl)butanoic acid
• Synonyms: 4-(3-hydroxy-4-methoxyphenyl)butanoic acid
• CAS NO: 57596-01-7
• Molecular Weight: 210.23
• Mol File: 57596-01-7.mol

Chemical Properties

• CAS DataBase Reference: 4-(3-hydroxy-4-methoxyphenyl)butanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(3-hydroxy-4-methoxyphenyl)butanoic acid(57596-01-7)
• EPA Substance Registry System: 4-(3-hydroxy-4-methoxyphenyl)butanoic acid(57596-01-7)

Safety Data

• Hazardous Substances Data: 57596-01-7(Hazardous Substances Data)

Upstream product

• 1403560-03-1 4-(3-acetoxy-4-methoxyphenyl)-4-oxobutyric acid 
• 613-70-7 2-methoxyphenyl acetate 
• 621-59-0 isovanillin 
• 98799-44-1 trans 4-(3-hydroxy-4-methoxyphenyl)but-3-enoic acid 

Downstream Products

• 15288-02-5 6-hydroxy-7-methoxy-1-tetralone 
• 1403560-04-2 4-(3-benzyloxy-4-methoxyphenyl)butyric acid 
• 1064207-26-6 6-benzyloxy-7-methoxy-1-tetralone 
• 96400-70-3 2-benzyloxy-3,8,9-trimethoxy-5-methyl-5,6-dihydrobenzo[c]phenanthridin-6-one 
• 119123-67-0 methyl 4-(3-benzyloxy-4-methoxyphenyl)butyrate 
• 1403560-11-1 C₁₂H₁₆O₄ 
• 98799-68-9 2-(6-Isopropoxy-7-methoxy-1-oxo-1,2,3,4-tetrahydro-naphthalen-2-yl)-3,4,5-trimethoxy-benzoic acid 
• 52259-72-0 norfagaronine 

Relevant articles and documents

Synthesis of benzo[c]phenanthridine alkaloids by Pd(OAc) 2-induced direct aromatic carbonylation

The Pd(OAc)2-induced carbonylation of alkoxy-substituted 1-amino-2-phenyltetralins and 1-amino-2-phenylnaphthalenes was examined to provide the benzo[c]phenanthridine ring system. The carbonylation of substrates containing methylenedioxy groups

Direct Synthesis of Benzophenanthridines and Benzophenanthridones via SRN1 Reactions

A straightforward and high-yield route to the 11,12-dihydrobenzophenanthridine (3) and 11,12-dihydrobenzophenanthridone (14) ring systems is based upon an SRN1 reaction between 2-halobenzylamines 1 or 2-halobenzoic acids 11 and enolates derived from tetralones 2.The efficient dehydrogenation of 3 or 14 gives the benzophenthridines 4 or benzophenanthridones 15.Use of properly substituted reactants leads to nitidine, avicine, and fagaronine and to analogues of those natural products.