2890-62-2

Basic information

• Product Name: 1-Acetyl-1-methylcyclohexane
• Synonyms: 1-Acetyl-1-methylcyclohexane;1-(1-Methylcyclohexyl)ethanone
• CAS NO: 2890-62-2
• Molecular Formula: C₉H₁₆O
• Molecular Weight: 140.22
• Mol File: 2890-62-2.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 186.2°C (estimate)
• Appearance: /
• Density: 0.9504
• Refractive Index: 1.4543
• CAS DataBase Reference: 1-Acetyl-1-methylcyclohexane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Acetyl-1-methylcyclohexane(2890-62-2)
• EPA Substance Registry System: 1-Acetyl-1-methylcyclohexane(2890-62-2)

Safety Data

• Hazardous Substances Data: 2890-62-2(Hazardous Substances Data)

Usage

General Description

1-Acetyl-1-methylcyclohexane is a chemical compound with the molecular formula C9H16O. It is a colorless liquid that is commonly used as a solvent in industrial and laboratory settings. It is also used as a fragrance ingredient in a variety of personal care products and perfumes. 1-Acetyl-1-methylcyclohexane is derived from cyclohexane, which is a six-membered cyclic hydrocarbon, and it is modified with an acetyl group and a methyl group. 1-Acetyl-1-methylcyclohexane is known for its pleasant odor and is often used to add fragrance to various products. It is important to handle this chemical with caution, as it can be harmful if ingested, inhaled, or comes in contact with the skin or eyes.

Upstream product

• 6555-61-9 1-(1-methylcyclohexyl)ethan-1-ol 
• 6555-59-5 (1-methylcyclohex-4-en-1-yl)-methyl-keton 
• 1124-96-5 2-(1-hydroxycyclohexyl)propan-2-ol 
• 506-82-1 dimethylcadmium 
• 2890-61-1 1-methyl-1-cyclohexancarboxylic acid chloride 
• 1189-71-5 isocyanate de chlorosulfonyle 
• 1123-25-7 1-methyl-1-cyclohexanecarboxylic acid 
• 917-54-4 methyllithium 
• 5749-72-4 isopropylidenecyclohexane 
• 77320-49-1 2-(1-Hydroxy-spiro[2.5]oct-1-yl)-malonic acid diethyl ester 
• 75-16-1 methylmagnesium bromide 
• 42393-50-0 1-(1-Hydroxy-1-methylethyl)-1-bromcyclohexan 
• 173547-35-8 3-Acetyl-3-methylcyclohexanone 
• 193818-70-1 3-(3-iodopropyl)-3-methylpent-4-en-2-one 

Downstream Products

• 27331-02-8 2-(1-methyl-cyclohexyl)-propan-2-ol 
• 1123-25-7 1-methyl-1-cyclohexanecarboxylic acid 
• 4926-90-3 1-methyl-1-ethylcyclohexane 
• 6555-61-9 1-(1-methylcyclohexyl)ethan-1-ol 
• 2890-64-4 1-Methylcyclohexylmethylketoxim 
• 359804-14-1 (1-methyl-cyclohexyl)-glyoxylic acid 
• 91351-46-1 1-(1-methyl-cyclohexyl)-ethanone semicarbazone 
• 28509-10-6 1-ethynyl-1-methylcyclohexane 
• 80605-96-5 1-Methylcyclohexylmethylketoxim-pikrat 
• 16580-26-0 1-methyl-1-isopropylcyclohexane 
• 16580-19-1 1-Methyl-1-(1-methylethenyl)cyclohexane 
• 2890-61-1 1-methyl-1-cyclohexancarboxylic acid chloride 
• 42253-14-5 2-bromo-1-(1-methyl-1-cyclohexyl)-1-ethanone 
• 1401206-01-6 1-(1-methylcyclohexyl)ethanol 

Relevant articles and documents

Synthesis of Vicinal Quaternary All-Carbon Centers via Acid-catalyzed Cycloisomerization of Neopentylic Epoxides

We report our studies on the development of a catalytic cycloisomerization of 2,2-disubstituted neopentylic epoxides to produce highly substituted tetralins and chromanes. Termination of the sequence occurs via Friedel-Crafts-type alkylation of the remote (hetero)arene linker. The transformation is efficiently promoted by sulfuric acid and proceeds best in 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) as the solvent. Variation of the substitution pattern provided detailed insights into the migration tendencies and revealed a competing disproportionation pathway of dihydronaphthalenes.

Enantioselective borohydride reduction of aliphatic ketones catalyzed by ketoiminatocobalt(iii) complex with 1-chlorovinyl axial ligand

For the enantioselective borohydride reduction of aliphatic ketones, the optically active ketoiminatocobalt(II) catalysts was successfully designed based on their axial ligand. Instead of chloroform for the aryl ketone reduction, various axial ligand precursors were examined for the aliphatic ketone. Consequently, 1, 1, 1-trichloroethane was found to be the most effective activator of the cobalt(II) complexes to generate the corresponding 1-chlorovinyl cobalt(III) derivatives as the reactive intermediate. Several aliphatic ketones were successfully reduced to afford the corresponding secondary alcohols with high enantioselectivities.

THERAPEUTIC AGENT FOR DIABETES

A therapeutic agent for diabetes, which comprises a compound of the formula [I] wherein Xis a group of the formula wherein R4and R5are the same or different and each is a hydrogen atom, an optionally substituted alkyl having 1 to 5 carbon atoms and the like, and R6is a hydrogen atom or an amino-protecting group; R1is an optionally substituted alkyl having 1 to 5 carbon atoms, an optionally substituted alkenyl having 2 to 6 carbon atoms and the like, R2is a hydrogen atom, an optionally substituted alkyl having 1 to 5 carbon atoms and the like, R2' is a hydrogen atom, and R3is an optionally substituted alkyl having 1 to 5 carbon atoms and the like, a prodrug thereof, a pharmaceutically acceptable salt thereof, a hydrate thereof and a solvate thereof. The compound of the present invention shows superior blood sugar decreasing action on the state of hyperglycemia, but does not affect the blood sugar when it is in the normal range or in the hypoglycemic state, which means that it is free of serious side effects such as hypoglycemia. Therefore, the compound of the present invention is useful as a therapeutic drug for diabetes and also useful as a preventive of the chronic complications of diabetes.