39257-08-4

Basic information

• Product Name: Cyclohexanone, 2,2,3-trimethyl-
• CAS NO: 39257-08-4
• Molecular Formula: C9H16O
• Molecular Weight: 140.225
• Mol File: 39257-08-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 2,2,3-trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 2,2,3-trimethyl-(39257-08-4)
• EPA Substance Registry System: Cyclohexanone, 2,2,3-trimethyl-(39257-08-4)

Safety Data

• Hazardous Substances Data: 39257-08-4(Hazardous Substances Data)

Upstream product

• 144406-32-6 2,2,3-trimethylstannyl-3-trimethylstannylcyclohexanone 
• 1551-89-9 trans-2,3-dimethylcyclohexanone 
• 98361-28-5 2,3-dimethyl-1-trimethylsilyloxycyclohexene 
• 74-88-4 methyl iodide 
• 1121-18-2 2-methyl-2-cyclohexen-1-one 
• 54313-25-6 4-penten-1-yllithium 
• 1120-72-5 2-Methylcyclopentanone 
• 112126-29-1 2-Methyl-1-(1-methyl-1-methylselanyl-ethyl)-cyclopentanol 
• 39256-99-0 2-methyl-7-octen-3-one 
• 412016-77-4 1-(α-hydroxy-isopropyl)-2-methyl-cyclopentanol 

Downstream Products

• 100428-69-1 (+/-)-cis-2,2,3-trimethyl-6-methylene-cyclohexylacetaldehyde 
• 91055-80-0 3,3,4-trimethylcyclohex-1-enecarbaldehyde 
• 96715-00-3 1,1,2-Trimethyl-5-methylen-6-acetonyl-cyclohexan 
• 92370-89-3 6-(Isobutyloxy-methylen)-2,2,3-trimethyl-cyclohexanon-⁽¹⁾ 
• 112967-39-2 3,3,4-trimethyl-1-cyclohexenyl methyl vinyl ether 
• 92037-13-3 1,1,2-Trimethyl-5-methylen-6-(β-hydroxy-ethyl)-cyclohexan 
• 90974-65-5 1-hydroxymethyl-3,3,4-trimethyl-1-cyclohexene 
• 107233-35-2 6-Hydroxy-methylen-2,2,3-trimethyl-cyclohexanon-⁽¹⁾ 

Relevant articles and documents

Access to 1,2-diketones by an unusual radical cascade

An unusual radical fragmentation of an unstrained cyclohexane structure was observed leading to complex 1,2-diketones.

Dependence of the Lewis Acid-induced Reaction of β-stannyl Ketones upon Substitution Pattern. 1,2-Alkyl Migration versus Cyclopropanation

3-Stannylcyclohexanones fully substituted at 2 and 3 positions undergo a 1,2-alkyl migration and cyclopropanation.The balance of the reaction pattern depends upon the steric environment and migratory aptitude of the alkyl groups.

Cycloaliphatic unsaturated ketones as odour- and taste-modifying agents

Process for the preparation of unsaturated cycloaliphatic ketones useful as perfuming and odour-modifying agents in the manufacture of perfumes and perfumed products, and as flavouring and taste-modifying agents in the aromatization of foodstuffs in general and imitation flavours for foodstuffs, beverages, animal feeds, pharmaceutical preparations and tobacco products. Compositions of matter relating to some of said unsaturated cycloaliphatic ketones which are new, and perfume- and flavouring compositions containing same.