125532-06-1

Basic information

• Product Name: Ethanone, 1-[4-(diethoxymethyl)phenyl]-
• CAS NO: 125532-06-1
• Molecular Formula: C13H18O3
• Molecular Weight: 222.284
• Mol File: 125532-06-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[4-(diethoxymethyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[4-(diethoxymethyl)phenyl]-(125532-06-1)
• EPA Substance Registry System: Ethanone, 1-[4-(diethoxymethyl)phenyl]-(125532-06-1)

Safety Data

• Hazardous Substances Data: 125532-06-1(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-[4-(diethoxymethyl)phenyl]- is a chemical compound with the molecular formula C14H18O3. It is a derivative of ethanone, or acetone, with a substituted phenyl group containing diethoxymethyl groups attached at the para position. Ethanone, 1-[4-(diethoxymethyl)phenyl]- is used in various industrial and research applications, including as a precursor for the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also used in the production of polymers and as a solvent in chemical reactions. The presence of the diethoxymethyl group makes this compound potentially useful in organic synthesis and as a building block for more complex molecules.

Upstream product

• 13411-48-8 1-(trimethylsilyl)ethanone 
• 34421-94-8 4-bromobenzaldehyde diethyl acetal 
• 81172-89-6 terephthalaldehyde mono(diethylacetal) 
• 125532-05-0 1-<4-(diethoxymethyl)phenyl>ethanol 

Downstream Products

• 147622-33-1 4'-diethylacetal-2-diphenylphosphino-acetophenone 
• 628311-43-3 (E)-4-[3-(2,4-dichloro-phenyl)-acryloyl]-benzaldehyde 
• 141200-79-5 5-{4-[1-[(Z)-Benzyloxyimino]-3-(5-methyl-2-phenyl-oxazol-4-yl)-propyl]-benzyl}-thiazolidine-2,4-dione 
• 125531-50-2 5-[1-(4-{3-[5-Methyl-2-(4-trifluoromethyl-phenyl)-oxazol-4-yl]-propionyl}-phenyl)-meth-(Z)-ylidene]-thiazolidine-2,4-dione 
• 125532-04-9 5-<4-<3-(5-methyl-2-phenyl-4-oxazolyl)-1-(methoxyimino)propyl>benzyl>thiazolidine-2,4-dione 
• 125531-49-9 5-[1-{4-[3-(5-Methyl-2-naphthalen-2-yl-oxazol-4-yl)-propionyl]-phenyl}-meth-(Z)-ylidene]-thiazolidine-2,4-dione 
• 125549-29-3 5-{4-[1-[(Z)-Hydroxyimino]-3-(5-methyl-2-phenyl-oxazol-4-yl)-propyl]-benzyl}-thiazolidine-2,4-dione 
• 125531-59-1 5-[1-(4-{3-[2-(4-Methoxy-phenyl)-5-methyl-oxazol-4-yl]-propionyl}-phenyl)-meth-(Z)-ylidene]-thiazolidine-2,4-dione 
• 125531-74-0 5-<4-<3-(5-methyl-2-phenyl-4-oxazolyl)-1-hydroxypropyl>benzyl>thiazolidine-2,4-dione 
• 125531-48-8 5-[1-{4-[3-(5-Methyl-2-p-tolyl-oxazol-4-yl)-propionyl]-phenyl}-meth-(Z)-ylidene]-thiazolidine-2,4-dione 
• 141199-92-0 5-{4-[3-(4-Benzyloxy-phenyl)-propionyl]-benzyl}-thiazolidine-2,4-dione 
• 141200-24-0 Darglitazone 
• 125531-60-4 5-[1-{4-[3-(5-Methyl-2-thiophen-2-yl-oxazol-4-yl)-propionyl]-phenyl}-meth-(Z)-ylidene]-thiazolidine-2,4-dione 
• 125531-61-5 5-[1-{4-[3-(2-Furan-2-yl-5-methyl-oxazol-4-yl)-propionyl]-phenyl}-meth-(Z)-ylidene]-thiazolidine-2,4-dione 

Relevant articles and documents

Palladium-catalyzed acetylation of arenes

A simple method for the preparation of aryl methyl ketones is reported. The transformation involves the Pd-catalyzed coupling of an acyl anion equivalent, acetyltrimethylsilane, with aryl bromides to afford the corresponding acetylated arenes in synthetically useful yields. The methodology is tolerant of heterocycles and provides a new method for arene functionalization.

Synthesis and coordination properties of novel polyfunctional phosphine ligands

4′-formyl-2-diphenylphosphino-acetophenone 5 has been prepared in four steps (50%) starting from terephtalaldehyde mono-(diethylacetal) 1. Condensation of 5 with the para-substituted anilines H2NA-i gives quantitatively the phosphine-imines 6-8