1041810-71-2

Basic information

• Product Name: (Z)-3-chloro-3-(4-methoxyphenyl)-2-(p-tolyl)propenal
• Synonyms: (Z)-3-chloro-3-(4-methoxyphenyl)-2-(p-tolyl)propenal
• CAS NO: 1041810-71-2
• Molecular Weight: 286.758
• Mol File: 1041810-71-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (Z)-3-chloro-3-(4-methoxyphenyl)-2-(p-tolyl)propenal(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-3-chloro-3-(4-methoxyphenyl)-2-(p-tolyl)propenal(1041810-71-2)
• EPA Substance Registry System: (Z)-3-chloro-3-(4-methoxyphenyl)-2-(p-tolyl)propenal(1041810-71-2)

Safety Data

• Hazardous Substances Data: 1041810-71-2(Hazardous Substances Data)

Upstream product

• 57297-25-3 1-(4-methoxyphenyl)-2-(4-methylphenyl)ethanone 
• 68-12-2 N,N-dimethyl-formamide 
• 622-47-9 4-tolylacetic acid 
• 100-66-3 methoxybenzene 

Downstream Products

• 1041811-21-5 C₁₇H₁₅NOSe 

Relevant articles and documents

Further studies on the application of vinylogous amides and β-halovinylaldehydes to the regiospecific synthesis of unsymmetrical, polyfunctionalized 2,3,4- and 1,2,3,4- substituted pyrroles

Highly functionalized pyrroles with appropriate regiochemical functionality represent an important class of marine natural products and potential drug candidates. We describe herein a detailed study of the reaction of α-aminoacid esters with vinylogous amides and also β-halovinylaldehydes for the regiospecific synthesis of 2,3,4-trisubstituted and 1,2,3,4-tetrasubstituted pyrroles. Since the vinylogous amides and β-halovinylaldehydes are readily available precursors, rapid access to a wide variety of unsymmetrically substituted pyrroles is accomplished via this methodology.