70017-27-5

Basic information

• Product Name: 2-Propenal, 3-(2,4-dichlorophenyl)-, (E)-
• CAS NO: 70017-27-5
• Molecular Formula: C9H6Cl2O
• Molecular Weight: 201.052
• Mol File: 70017-27-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-Propenal, 3-(2,4-dichlorophenyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenal, 3-(2,4-dichlorophenyl)-, (E)-(70017-27-5)
• EPA Substance Registry System: 2-Propenal, 3-(2,4-dichlorophenyl)-, (E)-(70017-27-5)

Safety Data

• Hazardous Substances Data: 70017-27-5(Hazardous Substances Data)

Upstream product

• 874-42-0 2,4-dichlorobenzaldeyhde 
• 75-07-0 acetaldehyde 
• 20595-45-3 2,4-dichlorocinnamic acid 
• 98581-93-2 3-(2',4'-dichlorophenyl)propionaldehyde 
• 3054-95-3 acrylaldehyde diethyl acetal 
• 29898-32-6 2,4-dichloro-1-iodo-benzene 

Downstream Products

• 93863-46-8 6-(2,4-dichlorophenyl)-4-hydroxy-5-hexen-2-one 
• 148775-23-9 (2E)-3-(2,4-dichlorophenyl)prop-2-en-1-ol 
• 1346682-13-0 (E)-1-(3-bromoprop-1-enyl)-2,4-dichlorobenzene 
• 1169949-29-4 (3S,4R)-9-benzyl-4-(2,4-dichlorophenyl)-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde 
• 1169949-05-6 (3S,4R)-9-benzyl-4-(2,4-dichlorophenyl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde 
• 1169949-27-2 (3S,4R)-9-benzyl-4-(2,4-dichlorophenyl)-6-methoxy-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde 
• 1280199-16-7 (E)-1,1,1-trichloro-4-(2,4-dichlorophenyl)but-3-en-2-one 
• 1280199-27-0 (4S,6S)-4-(2,4-dichlorophenyl)-6-hydroxy-2-phenyl-6-(trichloromethyl)-5,6-di-hydro-4H-pyran-3-carbonitrile 

Relevant articles and documents

Iron-Catalyzed ?±,?-Dehydrogenation of Carbonyl Compounds

An iron-catalyzed α,β-dehydrogenation of carbonyl compounds was developed. A broad spectrum of carbonyls or analogues, such as aldehyde, ketone, lactone, lactam, amine, and alcohol, could be converted to their α,β-unsaturated counterparts in a simple one-step reaction with high yields.

Organocatalytic enantioselective multicomponent synthesis of pyrrolopiperazines

The first organocatalytic multicomponent synthesis of enantioenriched pyrrolopiperazines is reported. These biologically relevant fused tricyclic products were obtained under catalytic iminium activation through a reaction sequence involving an enantioselective Michael addition followed by an iminium ion trapping via Pictet-Spengler cyclization (MAPS sequence). Substantial possibilities for variation on the three reaction partners [β-keto ester, enal and N-(2-aminoethyl)pyrrole] along with excellent enantioselectivities are the highlights of the present transformation.

Direct oxidative conversion of 3-aryl propionaldehydes to 3-aryl acroleins promoted by SOMO catalysis

A new direct oxidative transformation of 3-aryl propionaldehydes to 3-aryl acroleins promoted by SOMO catalysis has been realized with high efficiency under mild reaction conditions.