61349-69-7

Basic information

• Product Name: Cyclopentanone, 2-(4-methoxyphenyl)-
• CAS NO: 61349-69-7
• Molecular Formula: C₁₁H₁₁FO₂
• Molecular Weight: 190.242
• Mol File: 61349-69-7.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 318.686 °C at 760 mmHg
• Flash Point: 146.536 °C
• Density: 1.294 g/cm³
• CAS DataBase Reference: Cyclopentanone, 2-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopentanone, 2-(4-methoxyphenyl)-(61349-69-7)
• EPA Substance Registry System: Cyclopentanone, 2-(4-methoxyphenyl)-(61349-69-7)

Safety Data

• Hazardous Substances Data: 61349-69-7(Hazardous Substances Data)

Usage

General Description

Cyclopentanone, 2-(4-methoxyphenyl)- is a chemical compound that belongs to the class of aromatic ketones. It is also known as 4'-methoxyacetophenone and is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds. This chemical is a colorless to pale yellow liquid with a sweet, floral, and fruity odor. It is primarily used as a fragrance ingredient in cosmetic and personal care products, as well as in flavorings and fragrances. Additionally, it is also used as a solvent and intermediate in the production of other chemicals. However, it is important to handle this compound with care, as it may pose health hazards and should be used in accordance with proper safety guidelines and regulations.

Upstream product

• 936-52-7 1-(N-morpholino)cyclopent-1-ene 
• 18649-43-9 4-methoxyphenyllead(IV) triacetate 
• 694-28-0 2-chlorocyclopentanone 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 2998-04-1 diallyl adipate 
• 75265-67-7 allyl 2-oxocyclopentane-1-carboxylate 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 120-92-3 cyclopentanone 
• 709-12-6 1-(p-methoxyphenyl)-1-cyclopentene 
• 78195-96-7 1-(4-methoxyphenyl)cyclopentan-1-ol 
• 70106-27-3 2-(4-methoxyphenyl)cyclobutan-1-one 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 933674-44-3 2-(4-methoxyphenyl)cyclopentanol 
• 1191-95-3 cyclobutanone 

Downstream Products

• 61321-34-4 2-(4-methoxyphenyl)-2-<2-(dimethylamino)ethyl>cyclopentanone hydrobromide 
• 381226-47-7 C₁₆H₂₀O₃ 
• 129098-68-6 (-)-6-(4-methoxyphenyl)tetrahydro-2H-pyran-2-one 
• 1253111-91-9 (2S,3S)-2-(4-methoxyphenyl)-2-(2-nitro-1-phenylethyl)cyclopentanone 
• 34665-81-1 5-hydroxy-5-(4-methoxyphenyl)valeric acid δ lactone 

Relevant articles and documents

Enantioselective Radical Ring-Opening Cyanation of Oxime Esters by Dual Photoredox and Copper Catalysis

Catalytic enantioselective chemical reactions involving highly reactive radical species remain largely unexplored. We report herein for the first time a novel enantioselective radical ring-opening cyanation of redox-active oxime esters by dual photoreodox

Regio- and enantioselective Baeyer-Villiger oxidation: Kinetic resolution of racemic 2-substituted cyclopentanones

A kinetic resolution of racemic 2-substituted cyclopentanones via highly regio- and enantioselective Baeyer-Villiger oxidation has been successfully developed. The reaction could afford the normal 6-substituted δ-lactones in up to 98% ee and >19/1 regioselectivity. Meanwhile, the unreacted ketones were recovered in excellent ee values (up to 98%). It represents the best results of the kinetic resolution of racemic 2-substituted cyclopentanones via nonenzymic asymmetric BV oxidation.

The 2-(2-Azidoethyl)cycloalkanone strategy for bridged amides and medium-sized cyclic amine derivatives in the Aubé-Schmidt reaction

2-(2-Azidoethyl)cycloalkanones afford bridged lactams in the Aubé-Schmidt reaction, sometimes in excellent yield, and solvolysis yields derivatives of medium-ring amines. Attempts to divert the Schmidt reaction with an arene-mediated fragmentation of the normal Schmidt intermediate have led to an initial example. Georg Thieme Verlag Stuttgart.