2658-92-6

Usage

Uses

Used in Food Industry:
2-(but-3-en-1-yl)-3-methylcyclohex-2-en-1-one is used as a synthetic flavoring agent for its fruity, floral, and woody aroma, enhancing the taste and smell of various food products.
Used in Cosmetic Industry:
2-(but-3-en-1-yl)-3-methylcyclohex-2-en-1-one is used as a fragrance ingredient in cosmetic products, providing a pleasant scent that is appreciated by consumers.
Used in Perfume Industry:
2-(but-3-en-1-yl)-3-methylcyclohex-2-en-1-one is used in perfumes to add depth and complexity to the scent, with its combination of fruity, floral, and woody notes.
Used in Household Products:
It is also utilized in household products such as air fresheners and cleaning agents to provide a fresh and appealing fragrance.
Safety Precautions:
It is important to handle 2-(but-3-en-1-yl)-3-methylcyclohex-2-en-1-one with care due to its potential to cause skin and eye irritation. Additionally, it should be stored away from heat and open flames, as it is a flammable substance.

Upstream product

• 4994-08-5 3-(3-Butenyl)-2-methyl-4-oxo-2-cyclohexen-1-carbonsaeure-ethylester 
• 78707-63-8 3-Allyl-3-methyl-2-methylene-cyclohexanone 
• 220283-99-8 3-but-3-enyl-2-methyl-4-oxo-cyclohex-2-enecarboxylic acid methyl ester 
• 35490-07-4 methyl 2-methyl-4-oxocyclohex-2-enecarboxylate 
• 487-51-4 4-carbethoxy-3-methyl-2-cyclohexen-1-one 
• 220283-98-7 4-methyl-6-oxo-cyclohex-4-ene-1,3-dicarboxylic acid dimethyl ester 
• 5162-44-7 1-bromo-4-butene 
• 69253-50-5 Diethyl-[2-(5-methyl-cyclohexa-1,4-dienyloxy)-ethyl]-amine 

Downstream Products

• 4505-58-2 2--3-methyl-cyclohexen-2-ol 
• 98361-49-0 C₁₁H₁₇⁽²⁾HO 
• 124941-48-6 2-(but-3-enyl)-3,3-dimethylcyclohexanone 
• 90740-17-3 2-(3-butenyl)-3-methyl-2-cyclohexenyl p-nitrobenzoate 
• 98361-52-5 C₁₈H₂₀⁽²⁾HNO₄ 
• 68946-57-6 (4aR,8aR)-8a-Hydroxy-4a-methyl-3,4,4a,5,8,8a-hexahydro-2H-naphthalen-1-one 
• 1371536-56-9 (E)-2-(5-azidopent-3-enyl)-3,3-dimethylcyclohexanone 
• 116089-02-2 1-methyl-3-<2-(3-butenyl)-3-methyl-2-cyclohexenyloxycarbonyl>pyridinium iodide 
• 116088-96-1 2-(3-butenyl)-3-methyl-2-cyclohexenyl nicotinate 

Relevant academic research and scientific papers

Stereocontrol in a combined allylic azide rearrangement and intramolecular schmidt reaction

Pre-equilibration of an interconverting set of isomeric allylic azides is coupled with an intramolecular Schmidt reaction to afford substituted lactams stereoselectively. The effect of substitution and a preliminary mechanistic study are reported. The syn

An efficient one-pot four-step domino reaction for the synthesis of C2-substituted 3-methylcyclohex-2-enones

An efficient one-pot four-step domino reaction of substituted β-ketoesters has been optimized giving rise to a large panel of C2-substituted 3-methylcyclohex-2-enones, an important scaffold for the preparation of various initiators for cationic or radical cyclizations. The developed methodology is quite general and applicable to a wide range of β-ketoester substrates, allowing the introduction of various functionalities at the C2 position of the 3-methylcyclohex-2-enones, in good to excellent yields.

Stereospecific total synthesis of amberketal and a homologue

Amberketal (1a) and acetal homologue (2a) have been synthesised from a commercially available methyl acetoacetate involving palladium catalysed cyclisation as a key step.

THE INFLUENCE OF HYDROGEN BONDING ON THE SOLVOLYTIC REACTIVITY OF NICOTINATES IN FLUORINATED ALCOHOLS

A systematic investigation of solvolytic reactivities of allylic and benzylic nicotinates and their N-methylated derivatives in 80percent EtOH, 97percent TFE and 97percent HFIP was undertaken.The nicotinates in 97percent HFIP are slightly more reactive th

Solvolysis of 2-Alkenyl-2-cyclohexenyl p-Nitrobenzoates

In an attempt to study possible ?-participation in allyl derivatives, 2-alkenyl-3-methyl-2-cyclohexenyl p-nitrobenzoates 6 and 7 were solvolyzed in 97 wt percent trifluoroethanol and 80 vol percent ethanol.These esters show in both solvents a solvolysis r

3-Methylcyclohex-2-enone Derivatives as Initiators of Cyclisation. Part 1. Introduction and Synthesis of 2-Substituted 3-methylcyclohex-2-enones

A series of C-2 substituted 3-methylcyclohex-2-enones has been prepared using the Hagemann ester route.A new synthesis of these compounds has been developed which involves the alkylation of the N,N-diethylaminoethyl ether of 1-hydroxy-5-methylcyclohexa-1,5-diene.The cyclohexenones have been converted into the corresponding α,β-epoxyketones using alkaline hydrogen peroxide.

CYCLIZATION OF 1,3-DISUBSTITUTED 2-(3-BUTENYL)-2-CYCLOHEXEN-1-OLS

The cationic cyclization cyclohexanols 8a-c gave mixtures of the octalinols 9a-c and 10a-c with 9a-c as a main products.By cyclization of the isomeric educts 13a-c, the same products were formed in different proportions.

ACID CATALYZED COPE REARRANGEMENTS OF 2-ACYL-1,5-DIENES

The Cope rearrangement of 1,5-dienes bearing acyl substitutents in the 2-position of the diene system is strongly accelerated by protic and Lewis acids.