1241859-97-1

Basic information

• Product Name: ethyl 4-(4-methoxyphenyl)-5-methyl-2-phenylfuran-3-carboxylate
• Synonyms: ethyl 4-(4-methoxyphenyl)-5-methyl-2-phenylfuran-3-carboxylate
• CAS NO: 1241859-97-1
• Molecular Weight: 336.387
• Mol File: 1241859-97-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: ethyl 4-(4-methoxyphenyl)-5-methyl-2-phenylfuran-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 4-(4-methoxyphenyl)-5-methyl-2-phenylfuran-3-carboxylate(1241859-97-1)
• EPA Substance Registry System: ethyl 4-(4-methoxyphenyl)-5-methyl-2-phenylfuran-3-carboxylate(1241859-97-1)

Safety Data

• Hazardous Substances Data: 1241859-97-1(Hazardous Substances Data)

Upstream product

• 13540-76-6 3-(4-methoxyphenyl)prop-1-yne 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 37614-59-8 4-(4-methoxyphenyl)prop-2-yn-1-ol 

Relevant articles and documents

Method for preparing tetrasubstituted furan compound based on carbon-hydrogen bond activation

The invention provides a method for preparing a tetrasubstituted furan compound based on carbon-hydrogen bond activation, belongs to the field of organic synthesis, and relates to a method for synthesizing a tetrasubstituted furan compound through a [3+2]

Transition-metal-catalyzed domino reactions: Efficient one-pot regiospecific synthesis of highly functionalized polysubstituted furans from electron-deficient alkynes and 2-Yn-1-ols

Based on the reactive behavior of different transition-metal catalysts, three methods for the synthesis of highly functionalized polysubstituted furan derivatives are presented: (i) copper(I) iodide catalyzed regiospecific synthesis of furan aldehydes/ketones from alkynols and diethyl but-2-ynedioate under atmospheric pressure; (ii) nano-Cu-catalyzed domino process for the regioselective synthesis of -carbonylfurans from readily accessible starting materials; (iii) silver-catalyzed one-pot cyclization in toluene at 50 C for the synthesis of furan derivatives. It was notably that all the domino reactions were smooth under mild conditions with commercially available catalysts, and afforded highly functionalized furans in moderate to good yields. As we know, furans derivatives are extremely useful organic molecules used as synthetic building blocks for the synthesis of more elaborate heterocyclic compounds. Georg Thieme Verlag Stuttgart.