1346660-51-2

Basic information

• Product Name: 1-(3-methoxy-4-acetoxyphenyl)-2-propen-1-yl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate
• Synonyms: 1-(3-methoxy-4-acetoxyphenyl)-2-propen-1-yl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate
• CAS NO: 1346660-51-2
• Molecular Weight: 372.461
• Mol File: 1346660-51-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(3-methoxy-4-acetoxyphenyl)-2-propen-1-yl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-methoxy-4-acetoxyphenyl)-2-propen-1-yl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate(1346660-51-2)
• EPA Substance Registry System: 1-(3-methoxy-4-acetoxyphenyl)-2-propen-1-yl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate(1346660-51-2)

Safety Data

• Hazardous Substances Data: 1346660-51-2(Hazardous Substances Data)

Upstream product

• 97-53-0 4-allylguaiacol 
• 1346660-49-8 4-(1-bromoallyl)-2-methoxyphenyl acetate 
• 10453-89-1 chrysanthemumic acid 
• 93-28-7 eugenol acetate 

Relevant articles and documents

Design and synthesis of novel pyrethriods containing eugenol moiety

A novel series of pyrethriods was designed and synthesized by connecting various eugenol derivatives to either a chrysanthematic acid or 2-(4-chlorophenyl)-3-methylbutanoic acid. The insecticidal activity of target compounds has been evaluated by an immersion method on the fourth instar larvae of Culex pipens quinquefasciatus. The results revealed that the larvae were sensitive to synthesized compounds. Varying substituents in both acid moiety and eugenol group resulted in new compounds that exhibited different contact toxicity. Compound 3a showed the highest activity and is currently under further investigation.