816462-34-7

Basic information

• Product Name: 3,4-dimethoxyphenylpropioloyl chloride
• Synonyms: 3,4-dimethoxyphenylpropioloyl chloride
• CAS NO: 816462-34-7
• Molecular Weight: 224.644
• Mol File: 816462-34-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3,4-dimethoxyphenylpropioloyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-dimethoxyphenylpropioloyl chloride(816462-34-7)
• EPA Substance Registry System: 3,4-dimethoxyphenylpropioloyl chloride(816462-34-7)

Safety Data

• Hazardous Substances Data: 816462-34-7(Hazardous Substances Data)

Upstream product

• 22511-06-4 3,4-dimethoxyphenylpropiolic acid 
• 20583-78-2 ethyl (E)-3,4-dimethoxycinnamate 
• 14737-89-4 3,4-dimethoxy-trans-cinnamic acid 
• 99873-50-4 2,3-dibromo-3-(3',4'-dimethoxy)-phenyl ethyl propanoate 

Downstream Products

• 146072-33-5 N-Trifluoroacetylaminobutyl-3-(3',4'-dimethoxyphenyl)propynamide 
• 6259-86-5 3,4-methylenedioxycinnamyl 3',4'-dimethoxyphenylpropiolate 
• 31786-43-3 1-(3,4-dimethoxyphenyl)-3,4-dihydro-3-hydroxymethyl-6,7-methylenedioxynaphthalene-2-carboxylic acid lactone 
• 31888-76-3 1-(3,4-dimethoxyphenyl)-3-hydroxymethyl-6,7-methylenedioxynaphthalene-2-carboxylic acid lactone 
• 146072-36-8 (2Z)-N-4-Aminobutyl-3-(3',4'-dimethoxyphenyl)prop-2-enamide 
• 146072-34-6 (2Z)-N-4-Trifluoroacetylaminobutyl-3-(3',4'-dimethoxyphenyl)prop-2-enamide 
• 1122102-07-1 1-[2,4-di(benzyloxy)-6-hydroxyphenyl]-3-(3,4-dimethoxyphenyl)prop-2-yn-1-one 

Relevant articles and documents

A Gold(I)-Catalyzed Hydroamination/Cycloisomerization Cascade: Concise Synthesis of (±)-seco-Antofine and (±)-Septicine

A concise and flexible procedure for the synthesis of highly functionalized N-heterocyclic 1,6-annulated 2-pyridones and 2,3-annulated 4-pyrimidinones has been elaborated through a gold-catalyzed tandem hydroamination/cycloisomerization cascade. This novel and highly efficient method allows the rapid construction of these diverse N-heterocyclic scaffolds starting from readily available building blocks, and shows a wide scope and good functional group tolerance. The total synthesis of (±)-seco-antofine and (±)-septicine were realized employing this strategy.

An efficient synthesis of neoflavonoid antioxidants based on Montmorillonite K-10 catalysis

A new approach to synthesis of neoflavonoids, based on a high yielding Montmorillonite K-10 catalyzed lactone ring forming cyclization process, is described. The utility of this methodology is exemplified by its employment in the preparation of the substituted 4-phenylneoflavonoids 1-8. The free radical scavenging properties of these substances were evaluated. The neoflavonoids 1 and 5, which mimic esculetin-type antioxidants, were observed to quench hydrazyl free radicals.

Synthesis of Amido-ureas and the Nature of Caracasanamide, the Hypotensive Principle of Verbesina caracasana

Syntheses of the (E)-1 and (Z)-2 forms of 1-(3-methylbut-2-enyl)-3-(4-butyl)urea, proposed structures for the natural hypotensive caracasanamide, have been carried out.The compounds were found not to be identical wit