2047-97-4

Basic information

• Product Name: Ethanone, 1-(2-methyl-1-cyclohexen-1-yl)-
• CAS NO: 2047-97-4
• Molecular Formula: C9H14O
• Molecular Weight: 138.21
• Mol File: 2047-97-4.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(2-methyl-1-cyclohexen-1-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(2-methyl-1-cyclohexen-1-yl)-(2047-97-4)
• EPA Substance Registry System: Ethanone, 1-(2-methyl-1-cyclohexen-1-yl)-(2047-97-4)

Safety Data

• Hazardous Substances Data: 2047-97-4(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-(2-methyl-1-cyclohexen-1-yl)-, also known as alpha-methylcyclohexenyl methyl ketone, is a chemical compound with the molecular formula C11H16O. It is a ketone with a cyclohexenyl group attached to the carbon chain, giving it unique aromatic and functional properties. Ethanone, 1-(2-methyl-1-cyclohexen-1-yl)- is commonly used in the fragrance industry as a scent modifier and enhancer due to its pleasant floral and fruity aroma. It is also used in the production of perfumes, essential oils, and other cosmetic products. Additionally, it can act as a flavoring agent in food and beverages, providing a sweet and fruity taste.

Upstream product

• 591-49-1 1-methylcyclohex-1-ene 
• 108-24-7 acetic anhydride 
• 628-92-2 Cycloheptene 
• 64-19-7 acetic acid 
• 64-18-6 formic acid 
• 15564-30-4 cis-1-Ethinyl-2-methyl-1-cyclohexanol 
• 2396-65-8 1,8-nonadiyn 
• 30502-73-9 2,8-nonanedione 
• 15564-30-4 1-ethynyl-2-methyl-1-cyclohexanol 
• 583-60-8 2-Methylcyclohexanone 
• 108-94-1 cyclohexanone 
• 75-16-1 methylmagnesium bromide 
• 122439-38-7 1-(2-bromocyclohex-1-en-1-yl)ethanone 
• 38127-47-8 2-bromocyclohex-1-ene-1-carbaldehyde 

Downstream Products

• 76480-15-4 1-isopropenyl-2-methylcyclohexene 
• 55169-91-0 Methyl-1-acetyl-2-propionyl-6-cyclohexen 
• 859183-53-2 Androstan 
• 202351-70-0 1-(2-methyl-1-cyclohexenyl)-3-trimethylsilyloxy-3-phenyl-1-propanone 

Relevant articles and documents

Natural products inspired synthesis of neuroprotective agents against H2O2-induced cell death

Stroke is a debilitating disease and the third leading cause of death in the USA, where over 2000 new stroke cases are diagnosed every day. Treatment options for stroke-related brain damage are very limited and there is an urgent need for effective neurop

Enabling the development of N-Heterocyclic Carbene (NHC) catalyzed reactions: Practical methods for the preparation of 1-acyl-2-alkylcycloalkenes from cycloalkanones

The synthesis of 1-acyl-2-alkylcycloalkenes from a variety of cycloalkanones has been achieved via either-keto enol phosphates or-bromoenones. Both methods exploit simple and readily scalable transformations allowing the preparation of the desired compoun

A Novel Hetero-Diels-Alder Approach towards Perhydro Quinolinones Bearing an Angular Methyl Group

The title compounds 9-11 were synthesized by a hetero Diels-Alder reaction using the sterically demanding diene 2 as a new building block. The effect of commonly used Lewis acids and the substitution pattern of various imines 5 on both the mechanism and t