1448461-04-8

Basic information

• Product Name: methyl (4E)-2-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]hept-4-enoate
• Synonyms: methyl (4E)-2-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]hept-4-enoate
• CAS NO: 1448461-04-8
• Molecular Weight: 350.398
• Mol File: 1448461-04-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl (4E)-2-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]hept-4-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (4E)-2-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]hept-4-enoate(1448461-04-8)
• EPA Substance Registry System: methyl (4E)-2-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]hept-4-enoate(1448461-04-8)

Safety Data

• Hazardous Substances Data: 1448461-04-8(Hazardous Substances Data)

Upstream product

• 476452-73-0 methyl [(1-phenyl-1H-tetrazol-5-yl)sulfonyl]acetate 
• 688317-98-8 trans-carbonic acid methyl ester pent-2-enyl ester 

Relevant articles and documents

Syntheses of the hexahydroindene cores of indanomycin and stawamycin by combinations of iridium-catalyzed asymmetric allylic alkylations and intramolecular diels-alder reactions

Short and concise syntheses of the hexahydroindene cores of the antibiotics indanomycin (X-14547 A) and stawamycin are presented. Key methods used are an asymmetric iridium-catalyzed allylic alkylation, a modified Julia olefination, a Suzuki-Miyaura coupling, and an intramolecular Diels-Alder reaction.