478011-21-1

Basic information

• Product Name: 6-Heptenoic acid, 3-hydroxy-5-methoxy-4-methyl-7-phenyl-, methyl ester, (4S,5S,6E)-
• CAS NO: 478011-21-1
• Molecular Formula: C16H22O4
• Molecular Weight: 278.348
• Mol File: 478011-21-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-Heptenoic acid, 3-hydroxy-5-methoxy-4-methyl-7-phenyl-, methyl ester, (4S,5S,6E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Heptenoic acid, 3-hydroxy-5-methoxy-4-methyl-7-phenyl-, methyl ester, (4S,5S,6E)-(478011-21-1)
• EPA Substance Registry System: 6-Heptenoic acid, 3-hydroxy-5-methoxy-4-methyl-7-phenyl-, methyl ester, (4S,5S,6E)-(478011-21-1)

Safety Data

• Hazardous Substances Data: 478011-21-1(Hazardous Substances Data)

Upstream product

• 478011-20-0 (E)-(2R,3S)-3-Methoxy-2-methyl-5-phenyl-pent-4-enethioic acid S-ethyl ester 
• 173377-13-4 (E)-(2R,3S)-3-Hydroxy-2-methyl-5-phenyl-pent-4-enethioic acid S-ethyl ester 
• 104-55-2 3-phenyl-propenal 
• 79-20-9 acetic acid methyl ester 
• 138694-19-6 (2R,3R,4E)-3-Methoxy-2-methyl-5-phenyl-4-pentenal 

Downstream Products

• 478011-19-7 (+)-E-2,E-6-(4R,5S)-3,5-dimethoxy-4-methyl-7-phenyl-hepta-2,6-dienoic acid methyl ester 
• 910131-53-2 (+)-E-(2R,3S)-5-methoxy-4-methyl-3-oxo-7-phenyl-hept-6-enoic acid methyl ester 

Relevant articles and documents

The first synthesis and antifungal activities of 9-methoxystrobilurin-type β-substituted β-Methoxyacrylate

The first synthesis of 9-methoxystrobilurin-type β-substituted MOAs was successfully achieved. A chiral oudemansin-type β-substituted MOA was also synthesized utilizing Mukaiyama's asymmetric aldol reaction. Antifungal activities of the synthesized compounds against several representative fungi were examined by disk-diffusion assay. As a result, unique and superior antifungal properties of 9-methoxystrobilurin-type β-substituted MOAs compared with those of oudemansin-type analogue were clearly revealed.