2808-12-0

Usage

Uses

Used in Fragrance Industry:
(Cyclohexyl-3) acetate de methyle is used as a fragrance ingredient for its fruity, floral scent, adding a pleasant aroma to perfumes and personal care products. Its ability to provide a fresh and appealing scent makes it a popular choice in the fragrance industry.
Used in Flavor and Food Industry:
In the flavor and food industry, (cyclohexyl-3) acetate de methyle is used as a flavoring agent. Its unique fruity and floral notes enhance the taste and aroma of various food and beverage products, contributing to a more enjoyable consumer experience.
These applications highlight the diverse utility of (cyclohexyl-3) acetate de methyle in different sectors, primarily driven by its distinctive sensory characteristics.

Upstream product

• 72049-87-7 3-<(methoxycarbonyl)(trimethylsilyl)methyl>cyclohexan-1-one 
• 104681-69-8 (dimethoxy-1,1 cyclohexane yl-3) acatate de methyle 
• 186581-53-3 diazomethane 
• 33646-18-3 dimethyl 2-(3-oxocyclohexyl)malonate 
• 930-68-7 cyclohexenone 
• 36850-80-3 [(1-methoxyvinyl)oxy]trimethylsilane 
• 82452-68-4 (cyclohexanone yl-3) dithioacetate de methyle 
• 18365-23-6 methyl 2-(tributylstannyl)acetate 
• 67-56-1 methanol 

Downstream Products

• 41031-88-3 (Z)-2-(2-pentenyl)-2-cyclopenten-1-one 
• 86576-86-5 methyl 3-hydroxycyclohexylacetate 
• 90534-65-9 methyl 2-(5-oxocyclohex-3-en-1-yl)acetate 

Relevant academic research and scientific papers

Rhodium-Catalyzed Annelation of Benzoic Acids with α,β-Unsaturated Ketones with Cleavage of C?H, CO?OH, and C?C Bonds

In the presence of a [Cp*RhCl2]2 catalyst, the Lewis acid In(OTf)3, and the mild base Na2CO3, aromatic carboxylates and α,β-unsaturated ketones undergo a unique hydroarylation/Claisen/retro-Claisen pr

BENZOYL-PIPERIDINE DERIVATIVES AS DUAL MODULATORS OF THE 5-HT2A AND D3 RECEPTORS

The present invention relates to compounds of formula (I) wherein R1 and A are as defined in the specification as dual modulators of the serotonin 5-HT2a and dopamine D3 receptors, their manufacture, pharmaceutical compositions containing them and their use as medicaments. Compounds of general formula (I) have high affinity for the dopamine D3 and serotonin (5-Hydroxytryptamine; 5-HT) 5-HT2A receptors and are effective in the treatment of psychotic disorders, as well as other diseases such as depression and anxiety, drug dependence, dementias and memory impairment.

An environmentally friendly procedure for Mukaiyama aldol and Mukaiyama-Michael reactions using a catalytic amount of DBU under solvent- and metal-free conditions

Mukaiyama aldol and Mukaiyama-Michael reactions can proceed smoothly in the presence of a catalytic amount of DBU (20% mmol), to afford the corresponding products in moderate to good yields. This solvent- and metal-free approach provides an environmentall

A versatile synthesis of bicyclo[2.2.2]octan-2-one derivatives

A novel sequence for the synthesis of substituted bicyclo[2.2.2]oct-5-en-2-one derivatives starting from substituted cyclohex-2-en-1-ones is presented. The Michael addition of malonic esters to an α,β-unsaturated ketone and an intramolecular aldol reactio

Highly regioselective addition of an ester enolate equivalent to α,β-unsaturated ketones: Selective formation of both isomers derived from 1,2- and 1,4-additions using α-stannyl ester with additives

The reaction of α-stannyl ester with α,β-unsaturated ketones in the presence of stannous chloride (SnCl2) and chlorosilanes (Me3SiCl or Me2SiCl2) gave 1,2- and 1,4-addition products, respectively.

A novel asymmetric synthesis of 2,5-dialkylpyrrolidines

ZnCl2-promoted cyclization of enamino ester 8 furnished a 1.5:1 mixture of pyrrolidines 9 and 10. NaBH4-reduction of this mixture gave cis and trans-2,5-dialkylpyrrolidines 12 and 13 in the ratio 2:1. The latter derivative was obtain

Tetracyclic pyrrole lactam derivatives

Disclosed are the compounds of formula I STR1 wherein R and R1 -R3 independently represent hydrogen or lower alkyl, and m represents the integer 2 or 3; their methods of preparation; pharmaceutical compositions thereof, and their use

Addition-1,4 d'enethiolates lithies de dithioesters aux cetones ethyleniques

Deprotonation of carboxylic dithioesters with LDA gives rise to thermally stable lithium thioenolates that have been submitted to the action of various enones under kinetic conditions.Selective carbon-1,4-addition has been observed.Lithium thioenolates ma

Convenient Synthesis of Jasmonoid Compounds from γ-(Trimethylsiloxy)butyronitrile

1,4-Dioxygenated compounds 4 are constructed by the addition of a Grignard reagent to γ-(trimethylsiloxy)nitriles 1,2, and 3 and subsequent hydrolysis.Oxidation of 4 with pyridinium chlorochromate or Jones reagent yields compounds 5 which are used to produce cyclopentenones 6.Methyl jasmonate and methyl dihydrojasmonate are made by the conjugate addition of silylated ketene acetal 9 to 6a and 6b, respectively, and subsequent protodesilylation. γ-Jasmolactone is also derived from 4a by oxidation with pyridinium dichromate in DMF followed by reduction with NaBH4 in ethanol.