53618-36-3

Basic information

• Product Name: Butanoic acid, 2-[(4-methoxyphenyl)methylene]-, ethyl ester
• CAS NO: 53618-36-3
• Molecular Formula: C14H18O3
• Molecular Weight: 234.295
• Mol File: 53618-36-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Butanoic acid, 2-[(4-methoxyphenyl)methylene]-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Butanoic acid, 2-[(4-methoxyphenyl)methylene]-, ethyl ester(53618-36-3)
• EPA Substance Registry System: Butanoic acid, 2-[(4-methoxyphenyl)methylene]-, ethyl ester(53618-36-3)

Safety Data

• Hazardous Substances Data: 53618-36-3(Hazardous Substances Data)

Upstream product

• 17145-91-4 triethyl 2-ethylphosphonoacetate 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 1310070-48-4 2-(4-methoxy-3-((4-phenethoxybenzamido)methyl)benzyl)butanoic acid 
• 1310070-47-3 2-(3-((4-(benzyloxy)benzamido)methyl)-4-methoxybenzyl)butanoic acid 
• 1000675-18-2 2-(4-methoxy-3-((2-phenylbenzamido)methyl)benzyl)butanoic acid 
• 1000675-17-1 2-(4-methoxy-3-((3-phenylbenzamido)methyl)benzyl)butanoic acid 
• 1310070-43-9 2-(4-methoxy-3-((2-phenoxybenzamido)methyl)benzyl)butanoic acid 
• 1310070-42-8 2-(4-methoxy-3-((3-phenoxybenzamido)methyl)benzyl)butanoic acid 
• 334013-94-4 2-(4-methoxy-3-((4-(trifluoromethoxy)benzamido)methyl)benzyl)butanoic acid 
• 1310070-38-2 C₃₀H₃₅NO₅ 
• 1310070-37-1 C₂₉H₃₃NO₅ 
• 1310070-36-0 C₂₈H₃₁NO₄ 
• 1310070-35-9 C₂₈H₃₁NO₄ 
• 1310070-33-7 C₂₈H₃₁NO₅ 
• 1310070-32-6 C₂₈H₃₁NO₅ 
• 1310070-30-4 C₂₃H₂₆F₃NO₅ 

Relevant articles and documents

Structure-based design, synthesis, and nonalcoholic steatohepatitis (NASH)-preventive effect of phenylpropanoic acid peroxisome proliferator- activated receptor (PPAR) α-selective agonists

A series of α-ethylphenylpropanoic acid derivatives was prepared as candidate peroxisome proliferator-activated receptor (PPAR) α-selective agonists, based on our PPARα/δ dual agonist 3 as a lead compound. Structure-activity relationship studies clearly indicated that the steric bulkiness and position of the distal hydrophobic tail part are critical for PPARα agonistic activity and PPARα selectivity, as had been predicted from a molecular-modeling study. A representative compound blocked the progression of nonalcoholic steatohepatitis (NASH) in an animal model.

Design, synthesis, and evaluation of potent, structurally novel peroxisome proliferator-activated receptor (PPAR) δ-selective agonists

A series of 3-(4-alkoxyphenyl)propanoic acid derivatives was prepared as candidate peroxisome proliferator-activated receptor (PPAR) δ-selective agonists, based on our previously discovered potent human PPARα/δ dual agonist TIPP-401 as a lead compound. Structure-activity relationship studies clearly indicated the importance of the chain length of the alkoxy group at the 4-position, and the n-butoxy compound exhibited the most potent PPARδ transactivation activity and highest PPARδ selectivity. The (S)-enantiomer of a representative compound exhibited extremely potent PPARδ transactivation activity, comparable with or somewhat superior to that of the known PPARδ-selective agonist, GW-501516. The representative compound regulated the expression of genes involved in lipid and glucose homeostasis, and should be useful not only as a chemical tool to study PPARδ function, but also as a candidate drug for the treatment of metabolic syndrome.

Preparation and biologic properties of α alkylcinnamic acids

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