6948-41-0

Usage

Class

Cyclohexanols

Physical state

Colorless, viscous liquid

Odor

Slightly floral

Uses

Fragrance ingredient in perfumes and personal care products, fresh and clean scent in household cleaners and air fresheners

Antimicrobial properties

Useful ingredient in disinfectants and sanitizers

Solvent

Used in various chemical processes

Versatility

Wide range of industrial and consumer applications

InChI:InChI=1/C10H20O/c1-9(2)6-5-7-10(3,4)8(9)11/h8,11H,5-7H2,1-4H3

Upstream product

• 1195-93-3 2,2,6,6-tetramethylcyclohexanone 
• 487-68-3 mesytaldehyde 
• 775-12-2 diphenylsilane 

Downstream Products

• 72535-85-4 dithiocarbonic acid S-methyl ester-O-(2,2,6,6-tetramethyl-cyclohexyl ester) 
• 78414-58-1 1-methoxy-2,2,6,6-tetramethylcyclohexane 
• 1195-93-3 2,2,6,6-tetramethylcyclohexanone 
• 825637-05-6 2-(allyloxy)-1,1,3,3-tetramethylcyclohexane 
• 825637-06-7 (+/-)-2-{[(2,2,6,6-tetramethylcyclohexyl)oxy]methyl}oxirane 
• 825637-07-8 1-[(2,2,6,6-tetramethylcyclohexyl)oxy]butan-2-one 
• 87887-18-1 1-(2,2,6,6-tetramethyl-cyclohexyloxy)-butan-2-ol 

Relevant academic research and scientific papers

ITACONIC ACID DERIVATIVES AND USES THEREOF IN TREATING AN INFLAMMATORY DISEASE OR A DISEASE ASSOCIATED WITH AN UNDESIRABLE IMMUNE RESPONSE

The invention relates to compounds of formula (I) and to their use in treating or preventing an inflammatory disease or a disease associated with an undesirable immune response: (I) wherein R A, R B, R C and R D

Copper-catalyzed hydrosilylation with a bowl-shaped phosphane ligand: Preferential reduction of a bulky ketone in the presence of an aldehyde

Chemical Equation Presented Hollywood bowl: A highly active copper catalyst with a bowl-shaped phosphane (bsp) ligand was used in the hydrosilylation reaction of bulky ketones. The preferential reduction of a bulky ketone in the presence of an unprotected aldehyde is unprecedented.

Oxidation of α-Substituted Cyclohexanols by Nitric Acid

The influence of α-substituents on the oxidative cleavage of cyclohexanol by nitric acid in the presence of copper(II) and vanadium(V) ions has been investigated.Following the initial oxidation to give the cyclohexanone, further reaction, leading to ring opening of the ketone, requires at least one α-hydrogen.Thus 2,2,6,6-tetramethylcyclohexanol is converted to the corresponding ketone whilst 2,2,6-trimethylcyclohexanol is oxidised to a mixture of dicarboxylic acids.The mechanisms of the oxidations are discussed and enolisation is shown to be the key to oxidative cleavage.For ketones that can give two alternative enols, reaction occurs predominantly via the more stable tautomer.