1383129-40-5

Basic information

• Product Name: N-(2,2-diethoxyethyl)-N-(4-methoxyphenyl)-3-(o-tolyl)propiolamide
• Synonyms: N-(2,2-diethoxyethyl)-N-(4-methoxyphenyl)-3-(o-tolyl)propiolamide
• CAS NO: 1383129-40-5
• Molecular Weight: 381.472
• Mol File: 1383129-40-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(2,2-diethoxyethyl)-N-(4-methoxyphenyl)-3-(o-tolyl)propiolamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,2-diethoxyethyl)-N-(4-methoxyphenyl)-3-(o-tolyl)propiolamide(1383129-40-5)
• EPA Substance Registry System: N-(2,2-diethoxyethyl)-N-(4-methoxyphenyl)-3-(o-tolyl)propiolamide(1383129-40-5)

Safety Data

• Hazardous Substances Data: 1383129-40-5(Hazardous Substances Data)

Upstream product

• 645-36-3 2,2-diethoxy-ethanamine 
• 7515-27-7 3-(2-methylphenyl)prop-2-ynoic acid 
• 625842-54-8 N-(2,2-diethoxyethyl)-4-methoxyaniline 
• 696-62-8 para-iodoanisole 

Downstream Products

• 1383129-63-2 1-(2,2-diethoxyethyl)-3-iodo-4-(o-tolyl)-1-azaspiro[4.5]deca-3,6,9-triene-2,8-dione 
• 1383128-83-3 2-(3-iodo-2,8-dioxo-4-(o-tolyl)-1-azaspiro[4.5]deca-3,6,9-trien-1-yl)acetaldehyde 
• 1383129-03-0 (6aS,10aR)-2-iodo-1-(o-tolyl)-6a,7-dihydropyrrolo[2,1-i]indole-3,6,8(5H)-trione 

Relevant articles and documents

Desymmetrization of cyclohexadienones viad-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction

Enantioselective desymmetrization of cyclohexadienones via a d-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction was realized. With 10 mol% of camphor-derived triazolium salt E and 10 mol% of DIEA, various substituted cyclohexadienones proceeded through an intramolecular Stetter reaction, affording tricyclic products in moderate to good yields and excellent ee.