1004-55-3

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
Ethanone, 1-(1-chlorocyclohexyl)is used as a building block in organic synthesis for the production of various pharmaceuticals and agrochemicals. Its unique structure allows it to be a key component in the creation of new and effective compounds for these industries.
Used in Chemical Reactions:
Ethanone, 1-(1-chlorocyclohexyl)is used as a solvent for various chemical reactions due to its high solubility in a wide range of organic solvents. This property makes it a valuable asset in the synthesis of complex molecules and the facilitation of certain chemical processes.
Used in Fragrance Industry:
Ethanone, 1-(1-chlorocyclohexyl)is used as a key ingredient in the manufacture of perfumes and other scented products. Its distinct aroma profile contributes to the creation of unique and appealing fragrances, making it an important component in the fragrance industry.

Upstream product

• 823-76-7 Cyclohexyl methyl ketone 
• 1674-10-8 1,2-dimethylcyclohexene 
• 98959-54-7 2-methyl-1-oxaspiro[2.5]octane-2-carbonitrile 
• 54683-51-1 1-methyl-2-methylenecyclohexyl hydroperoxide 
• 26473-57-4 (1-methoxyethylidene)cyclohexane 
• 98841-10-2 2-Hydroxy-2-<1-Chlor-cyclohexyl-(1)>-propionitril 

Downstream Products

• 1123-25-7 1-methyl-1-cyclohexanecarboxylic acid 
• 932-66-1 1-cyclohexenyl methyl ketone 
• 1209-42-3 1-methyl-cyclohexanecarboxylic acid phenyl ester 
• 40702-53-2 1-(1-amino-cyclohexyl)-ethanone 
• 64639-28-7 (1-trimethylsiloxyethylidene)cyclohexane 
• 7499-13-0 <1-Semicarbazo-ethyl-(1)>-cyclohexen-(1) 
• 1756-33-8 1-cyclohex-1-enyl-ethanone-(2,4-dinitro-phenylhydrazone) 
• 1123-27-9 1-(1-hydroxycyclohexyl)ethan-1-one 
• 927386-24-1 (R_S)-(-)-N-[1-(1-chlorocyclohexyl)ethylidene]-tert-butanesulfinamide 
• 927386-32-1 (R_S,R)-N-(1-phenylspiro[2.5]oct-1-yl)-tert-butanesulfinamide 
• 1123-26-8 1-(1'-hydroxyethyl)-1-cyclohexanol 

Relevant academic research and scientific papers

Regioselective radical cyclization initiated by the reaction of allylic hydroperoxides with iron(II) sulfate

Treatment of 1-methyl-2-methylene-1-cyclohexyl hydroperoxide with a mixture of FeSO4/CuCl2 yielded 1-(1-chlorocyclohexyl)ethanone as the major product consistent with 6-endo-trig cyclization of the intermediate 5-acetylhex-5-enyl rad

The Regiochemistry of the Radical Addition of N-Chloroamides to Enol Ethers

The orientation of the radical addition of N-chloroamides (ZCONHCl) to enol ethers was studied as a function of Z and the enol ether structure and compared with the orientation of radical addition of thioacetic acid and the orientation of typical electrop

The photochemical addition of N-haloamides to olefins: the influence of various factors on the competition between 1,2-addition and hydrogen abstraction

In the photodecomposition of N-haloamides (ZCONRX) in the presence of olefins, the 1,2-addition chain competes with the hydrogen abstraction chain(s) leading to the parent amide (the quantum yields for these processes are greater than unity).The following factors were shown to have an influence on this competition as measured by the yield of 1,2-addition and the yield of parent amide in methylene chloride solutions: (i) the N-halogen (higher yields of addition with X=Cl than with X=Br); (ii) the electronegativity of Z (increase of the yield of addition as the electronegativity of Z increases); (iii) the temperature (higher yields of addition at lower temperatures, and at -70 degC, better yields of addition (>90percent, R=H) for X=Br than for X=Cl); and (iv) the size of R (dramatic decrease of the yield of 1,2-addition in going from R=H to R=CH3).Surprisingly, the presence of a scavenger for HX had no influence on the yield of 1,2-addition.Both the size and electronegativity of Z had an effect on the stereochemistry of 1,2-addition to cyclohexene.High yields of addition to a variety of olefins were obtained with N-chloroamides such as ClCH2CONHCl, C2H5OCONHCl, CF3CONHCl.Their addition to enol ethers at -70 degC led to the synthesis of α-amido acetals or ketals (aldehydes or ketones) and to an α-amido glycoside in good yields.