647029-45-6

Basic information

• Product Name: (2S,3S)-2-Benzo[1,3]dioxol-5-ylmethyl-3-hydroxy-3-isopropyl-5-(4-methoxy-phenyl)-pent-4-ynal
• CAS NO: 647029-45-6
• Molecular Weight: 380.441
• Mol File: 647029-45-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3S)-2-Benzo[1,3]dioxol-5-ylmethyl-3-hydroxy-3-isopropyl-5-(4-methoxy-phenyl)-pent-4-ynal(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-2-Benzo[1,3]dioxol-5-ylmethyl-3-hydroxy-3-isopropyl-5-(4-methoxy-phenyl)-pent-4-ynal(647029-45-6)
• EPA Substance Registry System: (2S,3S)-2-Benzo[1,3]dioxol-5-ylmethyl-3-hydroxy-3-isopropyl-5-(4-methoxy-phenyl)-pent-4-ynal(647029-45-6)

Safety Data

• Hazardous Substances Data: 647029-45-6(Hazardous Substances Data)

Upstream product

• 2373-80-0 3,4-(methylenedioxy)cinnamic acid 
• 212712-42-0 (+)-(S)-4′′-benzyl-3′′-(3-(3′,4′-methylenedioxyphenyl)propanoyl)oxazolidin-2′′-one 
• 2815-95-4 3-(1,3 benzodioxol-5-yl)propionic acid 
• 68996-81-6 3-benzo[1,3]dioxol-5-yl-propionyl chloride 
• 120-57-0 piperonal 
• 647029-27-4 (4S)-4-benzyl-[(2S,3S)-3-hydroxy-5-(4-methoxyphenyl)-2-(3,4-methylenedioxybenzyl)-4-pentynoyl]-2-oxazolidinone 
• 647029-32-1 1-tert-butyldimethylsilyloxy-5-(4-methoxyphenyl)-2-(3,4-methylenedioxyphenyl)methyl-4-pentyn-3-ol 
• 647029-34-3 (2R)-1-tert-butyldimethylsilyloxy-5-(4-methoxyphenyl)-2-(3,4-methylenedioxyphenyl)methyl-4-pentyn-3-one 
• 647029-29-6 5-(4-methoxyphenyl)-2-(3,4-methylenedioxyphenyl)methyl-4-pentyne-1,3-diol 
• 647029-36-5 (2R)-1-hydroxy-5-(4-methoxyphenyl)-2-(3,4-methylenedioxyphenyl)methyl-4-pentyn-3-one 
• 647008-05-7 (2R,3S)-5-(4-methoxyphenyl)-2-(3,4-methylenedioxybenzyl)-3-(1-methylethyl)-4-pentyne-1,3-diol 

Downstream Products

• 647029-39-8 (2S,3S)-3-hydroxy-3-isopropyl-5-(4-methoxyphenyl)-2-(3,4-methylenedioxybenzyl)-4-pentynoic acid 

Relevant articles and documents

Systematic strategy for the synthesis of cyanobacterin and its stereoisomers. 1. Asymmetric total synthesis of dechloro-cyanobacterin and its enantiomer

The stereocontrolled total synthesis of the non-chlorinated analog of cyanobacterin, a potent photosynthesis inhibitor, was achieved by 12 steps in a 10.0% overall yield. Its enantiomer was also synthesized from the same starting material. This synthetic strategy is expected to be applicable to prepare cyanobacterin and all its stereoisomers, together with other similar bioactive compounds.