4046-09-7

Basic information

• Product Name: Ethanone, 1-(1-phenylcyclopentyl)-
• CAS NO: 4046-09-7
• Molecular Formula: C13H16O
• Molecular Weight: 188.269
• Mol File: 4046-09-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(1-phenylcyclopentyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(1-phenylcyclopentyl)-(4046-09-7)
• EPA Substance Registry System: Ethanone, 1-(1-phenylcyclopentyl)-(4046-09-7)

Safety Data

• Hazardous Substances Data: 4046-09-7(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-(1-phenylcyclopentyl)- is a chemical compound that belongs to the ketone class of organic compounds. It is derived from a cyclopentane ring with a phenyl substituent attached to one of the carbons, and a ketone functional group attached to another carbon. Ethanone, 1-(1-phenylcyclopentyl)- may have applications in various fields including pharmaceuticals, fragrances, and organic synthesis. Its chemical structure suggests it may have potential for use as a building block in the synthesis of complex molecules. Further research and studies are needed to fully understand its properties and potential uses.

Upstream product

• 110-52-1 1,4-dibromo-butane 
• 103-79-7 1-phenyl-acetone 
• 77-57-6 1-phenyl-1-cyclopentanecarbonitrile 
• 60021-45-6 Methyl-(1-phenyl-2-cyclopentenyl)-keton 
• 154382-30-6 β-oxo-1-phenylcyclopentanepropanoic acid ethyl ester 
• 77-55-4 1-phenyl-1-cyclopentanecarboxylic acid 
• 917-54-4 methyllithium 
• 75-16-1 methylmagnesium bromide 
• 917-64-6 methyl magnesium iodide 

Downstream Products

• 101266-82-4 1-(1-phenyl-cyclopentyl)-ethanol 
• 700-88-9 cyclopentylbenzene 
• 80606-91-3 1-Phenylcyclopentylmethylketoxim 
• 80606-01-5 1-Phenylcyclopentylmethylketoxim-pikrat 

Relevant articles and documents

Water-Soluble Calixarenes as New Inverse Phase-Transfer Catalysts. Their Scope in Aqueous Biphasic Alkylations and Mechanistic Implications

Alkylation reactions of active methylene compounds, alcohols and phenols with alkyl halides in aqueous NaOH solution can be carried out without the need for any added organic solvents in most cases. The water-soluble calix[n]arenes, which contain trimethylammoniomethyl groups on the upper rim, were used as inverse phase-transfer catalysts, resulting in the corresponding alkylated products in good to high yields. The scope of this methodology in aqueous biphasic alkylation reactions and the mechanistic implications are discussed.

Wanderungstendenzen cyclischer, polycyclischer und methylverzweigter Alkylreste bei der Beckmann-Umlagerung

The migration aptitudes of polycyclic bridgehead groups, cycloalkyl groups as well as of β-, γ- and δ-branched alkyl groups in the Chapman variant of the Beckmann rearrangement were determined.From these data it is concluded that at transition state 2 the migrating group is not resembling a planarised carbenium ion R+, but rather a pentacoordinated carbonium ion structure.Because only small geometrical changes occur in the migrating group vertical stabilisation of charge at transition state is believed to have significant influence on the migration aptitudes.