42036-05-5

Basic information

• Product Name: 1-Chlor-1-p-methoxy-phenyl-2-formyl-2-phenylaethylen
• Synonyms: 1-Chlor-1-p-methoxy-phenyl-2-formyl-2-phenylaethylen
• CAS NO: 42036-05-5
• Molecular Weight: 272.731
• Mol File: 42036-05-5.mol

Chemical Properties

• CAS DataBase Reference: 1-Chlor-1-p-methoxy-phenyl-2-formyl-2-phenylaethylen(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Chlor-1-p-methoxy-phenyl-2-formyl-2-phenylaethylen(42036-05-5)
• EPA Substance Registry System: 1-Chlor-1-p-methoxy-phenyl-2-formyl-2-phenylaethylen(42036-05-5)

Safety Data

• Hazardous Substances Data: 42036-05-5(Hazardous Substances Data)

Upstream product

• 1023-17-2 4-methoxyphenyl benzyl ketone 
• 103-82-2 phenylacetic acid 
• 100-66-3 methoxybenzene 

Downstream Products

• 52444-49-2 (Z)-1-(4-Methoxy-phenyl)-2-phenyl-3-phenylamino-propenethione 
• 40673-29-8 1-Mercapto-1-p-methoxyphenyl-2-formyl-2-phenylethylen 

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.