29643-34-3

Basic information

• Product Name: Ethanone, 1-(3-ethyl-4-methoxyphenyl)-
• CAS NO: 29643-34-3
• Molecular Formula: C11H14O2
• Molecular Weight: 178.231
• Mol File: 29643-34-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(3-ethyl-4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(3-ethyl-4-methoxyphenyl)-(29643-34-3)
• EPA Substance Registry System: Ethanone, 1-(3-ethyl-4-methoxyphenyl)-(29643-34-3)

Safety Data

• Hazardous Substances Data: 29643-34-3(Hazardous Substances Data)

Upstream product

• 110457-64-2 2,4-diethylanisole 
• 14804-32-1 2-ethylanisole 
• 75-36-5 acetyl chloride 
• 3056-59-5 acetate d'ethyl-2 phenyl 
• 90-00-6 o-Hydroxyethylbenzene 
• 22934-47-0 1-(3-ethyl-4-hydroxy-phenyl)-ethanone 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 105321-45-7 3-ethyl-4-methoxy-α-methylbenzylamine 
• 22934-36-7 methyl 3-ethyl-4-hydroxybenzoate 
• 95763-98-7 2-Aethyl-4-methoxycarbonyl-cyclohexanol 
• 105211-75-4 3-ethyl-4-hydroxybenzoic acid 
• 22934-35-6 3-ethyl-4-methoxybenzoic acid 
• 30195-60-9 3-Dimethylamino-1-(3-ethyl-4-methoxy-phenyl)-propan-1-one; hydrochloride 

Relevant articles and documents

Selective electrochemical oxidation of aromatic hydrocarbons and preparation of mono/multi-carbonyl compounds

A selective electrochemical oxidation was developed under mild condition. Various mono-carbonyl and multi-carbonyl compounds can be prepared from different aromatic hydrocarbons with moderate to excellent yield and selectivity by virtue of this electrochemical oxidation. The produced carbonyl compounds can be further transformed into α-ketoamides, homoallylic alcohols and oximes in a one-pot reaction. In particular, a series of α-ketoamides were prepared in a one-pot continuous electrolysis. Mechanistic studies showed that 2,2,2-trifluoroethan-1-ol (TFE) can interact with catalyst species and generate the corresponding hydrogen-bonding complex to enhance the electrochemical oxidation performance. [Figure not available: see fulltext.]

Substituted pyrazolyl benzenesulfonamides for use in veterinary therapies

A method of using pyrazolyl benzenesulfonamide compounds in treating inflammation and inflammation-related disorders in companion animals is disclosed.

Triazine derivatives, a process for preparing the derivatives, and herbicides containing the derivatives as the effective component

A triazine derivative represented by the general formula: STR1 wherein R1 and R2 are each an alkyl group having 1 to 4 carbon atoms, and X1 and X2 are each a halogen atom, an alkyl group having 1 to 4 carbon atoms, an alkoxyl group having 1 to 4 carbon atoms, or an alkylthio group having 1 to 4 carbon atoms. This invention also provides a process for efficiently preparing said triazine derivative and a herbicide containing said triazine derivative as effective component.