446874-39-1

Basic information

• Product Name: 3-(2-iodo-3,4,5-trimethoxy-phenyl)-N-methoxy-N-methyl-propionamide
• Synonyms: 3-(2-iodo-3,4,5-trimethoxy-phenyl)-N-methoxy-N-methyl-propionamide
• CAS NO: 446874-39-1
• Molecular Weight: 409.221
• Mol File: 446874-39-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-(2-iodo-3,4,5-trimethoxy-phenyl)-N-methoxy-N-methyl-propionamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-iodo-3,4,5-trimethoxy-phenyl)-N-methoxy-N-methyl-propionamide(446874-39-1)
• EPA Substance Registry System: 3-(2-iodo-3,4,5-trimethoxy-phenyl)-N-methoxy-N-methyl-propionamide(446874-39-1)

Safety Data

• Hazardous Substances Data: 446874-39-1(Hazardous Substances Data)

Upstream product

• 369405-57-2 N-methoxy-N-methyl-3-(3',4',5'-trimethoxyphenyl)propanamide 
• 66543-72-4 3-(3',4',5'-trimethoxyphenyl)propionyl chloride 
• 25173-72-2 3-(3,4,5-trimethoxyphenyl)propanoic acid 

Downstream Products

• 446874-44-8 1-{6-[3-(tert-butyl-dimethyl-silanyloxy)-5-trimethylsilanyl-pent-4-ynyl]-2,3,4-trimethoxy-phenyl}-5-diazo-pentane-1,4-dione 
• 446874-42-6 4-{6-[3-(tert-butyl-dimethyl-silanyloxy)-5-trimethylsilanyl-pent-4-ynyl]-2,3,4-trimethoxy-phenyl}-4-oxo-butyric acid 
• 446874-45-9 1-{6-[3-(tert-butyl-dimethyl-silanyloxy)-pent-4-ynyl]-2,3,4-trimethoxy-phenyl}-5-diazo-pentane-1,4-dione 
• 446874-43-7 4-{6-[3-(tert-butyl-dimethyl-silanyloxy)-pent-4-ynyl]-2,3,4-trimethoxy-phenyl}-4-oxo-butyric acid 
• 446874-41-5 1-[3-(tert-butyl-dimethyl-silanyloxy)-5-trimethylsilanyl-pent-4-ynyl]-2-iodo-3,4,5-trimethoxy-benzene 
• 446874-40-4 5-(2-iodo-3,4,5-trimethoxy-phenyl)-1-trimethylsilanyl-pent-1-yn-3-ol 
• 866897-67-8 tert-butyl(dimethyl)silyl[(1R)-1-[(2-iodo-3,4,5-trimethoxyphenyl)ethyl]-3-(trimethylsilyl)prop-2-ynyl]ether 
• 866897-66-7 (3R)-5-(2-iodo-3,4,5-trimethoxyphenyl)-1-(trimethylsilyl)pent-1-yn-3-ol 
• 866897-68-9 4-{6-[3-(tert-butyl-dimethyl-silanyloxy)-5-trimethylsilanyl-pent-4-ynyl]-2,3,4-trimethoxy-phenyl}-4-oxo-butyric acid 
• 866897-65-6 5-(2-iodo-3,4,5-trimethoxyphenyl)-1-(trimethylsilyl)pent-1-yn-3-one 

Relevant articles and documents

Facile construction of the colchicine skeleton by a rhodium-catalyzed cyclization/cycloaddition cascade

The major alkaloid of the meadow saffron is colchicine, which displays remarkable antimitotic activity and has long been used in the treatment of acute gout and is currently being tested against a broad variety of other diseases. In a remarkable Rh-cataly

Total syntheses of colchicine in comparison: A journey through 50 years of synthetic organic chemistry

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