1173997-34-6

Basic information

• Product Name: ethyl-4-[(1-phenyl-1H-tetrazole-5-yl)thio]butanoate
• Synonyms: ethyl-4-[(1-phenyl-1H-tetrazole-5-yl)thio]butanoate
• CAS NO: 1173997-34-6
• Molecular Weight: 292.362
• Mol File: 1173997-34-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: ethyl-4-[(1-phenyl-1H-tetrazole-5-yl)thio]butanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl-4-[(1-phenyl-1H-tetrazole-5-yl)thio]butanoate(1173997-34-6)
• EPA Substance Registry System: ethyl-4-[(1-phenyl-1H-tetrazole-5-yl)thio]butanoate(1173997-34-6)

Safety Data

• Hazardous Substances Data: 1173997-34-6(Hazardous Substances Data)

Upstream product

• 2969-81-5 Ethyl 4-bromobutyrate 
• 15052-19-4 5-mercapto-1-phenyl-1H-tetrazole sodium salt 

Downstream Products

• 1173997-10-8 ethyl 4-((1-phenyl-1H-tetrazol-5-yl)sulfonyl)butanoate 
• 156661-61-9 (-)-(R)-6-Methyl-9-phenyl-(E)-4-nonenoic acid ethyl ester 
• 1215664-16-6 ethyl (Z)-5-[4-(trifluoromethyl)phenyl]pent-4-enoate 

Relevant articles and documents

"One-pot" reductive lactone alkylation provides a concise asymmetric synthesis of chiral isoprenoid targets

An efficient method, based on nucleophilic addition to lactones followed by modified in situ Clemmensen reduction, provides a short synthetic route to chiral isoprenoid targets. The efficacy of this method has been exemplified through the synthesis of several targets including the commercial fragrance Rosaphen, the side chain of Zaragozic acid C, the cotton leaf sex pheromone, and the side chains of vitamin E.