95123-61-8

Basic information

• Product Name: 2-Propenal, 3-[4-(trifluoromethyl)phenyl]-, (2E)-
• CAS NO: 95123-61-8
• Molecular Formula: C10H7F3O
• Molecular Weight: 200.16
• Mol File: 95123-61-8.mol
• Article Data: 52

Chemical Properties

• CAS DataBase Reference: 2-Propenal, 3-[4-(trifluoromethyl)phenyl]-, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenal, 3-[4-(trifluoromethyl)phenyl]-, (2E)-(95123-61-8)
• EPA Substance Registry System: 2-Propenal, 3-[4-(trifluoromethyl)phenyl]-, (2E)-(95123-61-8)

Safety Data

• Hazardous Substances Data: 95123-61-8(Hazardous Substances Data)

Usage

General Description

2-Propenal, 3-[4-(trifluoromethyl)phenyl]-, (2E)- is a chemical compound with the molecular formula C10H7F3O. It is also known as 3-(4-trifluoromethylphenyl)-2-propenal and is classified as an alpha, beta-unsaturated aldehyde. 2-Propenal, 3-[4-(trifluoromethyl)phenyl]-, (2E)- is commonly used in the synthesis of pharmaceuticals and agrochemicals, and also has applications in the production of fragrances and flavorings. It is known to have potential toxic effects and should be handled with care. Additionally, it is important to note that this compound may have specific regulations regarding its handling and disposal, and should be used in accordance with proper safety protocols.

Upstream product

• 455-13-0 4-Iodobenzotrifluoride 
• 20461-86-3 2,2-diethoxy acetic acid 
• 1059140-27-0 1-(2-bromovinyl)-4-(trifluoromethyl)benzene 
• 298-12-4 Glyoxilic acid 
• 352525-91-8 trans-2-[4-(trifluoromethyl)phenyl]vinylboronic acid 
• 1813-97-4 1-allyl-4-(trifluoromethyl)benzene 
• 201230-82-2 carbon monoxide 
• 705-31-7 4-trifluoromethylphenylacetylene 
• 83494-26-2 α-ethynyl-4-(trifluoromethyl)-benzenemethanol 
• 455-19-6 4-Trifluoromethylbenzaldehyde 
• 75-07-0 acetaldehyde 
• 3054-95-3 acrylaldehyde diethyl acetal 
• 149946-79-2 1-(4'-(trifluoromethyl)phenyl)-allylalcohol 
• 166947-09-7 3-(4-trifluoromethylphenyl)propanal 

Downstream Products

• 1095273-18-9 ethyl 2-(4-formyl-1-tosyl-5-(4-(trifluoromethyl)phenyl)pyrrolidin-3-yl)acetate 
• 1195315-12-8 (R)-2-(4-(trifluoromethyl)phenyl)-2H-chromene-3-carbaldehyde 
• 1245793-04-7 6-isopropyl-2-phenyl-3,5-di(4-trifluoromethylphenylmethyl)-4H-pyran-4-one 
• 1255189-05-9 C₁₂H₉F₃OS 

Relevant articles and documents

Crossed Regio- and Enantioselective Iron-Catalyzed [4+2]-Cycloadditions of Unactivated Dienes

The cyclohexene motif is ubiquitous in nature and specialty chemicals. A straightforward selective access to chiral cyclohexenes from unactivated dienes and dienophiles is not feasible by classical Diels–Alder reaction and constitutes an unsolved syntheti

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.

Asymmetric Synthesis of Functionalized 9-Methyldecalins Using a Diphenylprolinol-Silyl-Ether-Mediated Domino Michael/Aldol Reaction

Substituted 9-methyldecalin derivatives containing an all carbon quaternary chiral center were synthesized with excellent enantioselectivity via an organocatalyst-mediated domino reaction. The first reaction is a diphenylprolinol silyl ether-mediated Michael reaction, and the second reaction is an intramolecular aldol reaction. The enantiomerically pure catalyst is involved in both reactions.