6493-80-7

Usage

Uses

Used in Food and Beverage Industry:
Methyl 1-methylcyclohex-3-ene-1-carboxylate is used as a flavoring agent for adding a fruity and sweet aroma to food and beverage products. Its pleasant scent enhances the overall taste and aroma experience of these products, making them more appealing to consumers.
Used in Perfume and Fragrance Industry:
In the perfume and fragrance industry, methyl 1-methylcyclohex-3-ene-1-carboxylate is used as a key ingredient to create unique and captivating scents. Its fruity and sweet aroma contributes to the complexity and depth of perfumes, colognes, and other fragrances, making them more attractive and long-lasting.
Used in Organic Compound Production:
Methyl 1-methylcyclohex-3-ene-1-carboxylate is also used as a solvent in the production of various organic compounds. Its ability to dissolve a wide range of substances makes it a versatile and useful component in chemical synthesis and processing.
Safety Considerations:

InChI:InChI=1/C9H14O2/c1-9(8(10)11-2)6-4-3-5-7-9/h3-4H,5-7H2,1-2H3

Upstream product

• 106-99-0 buta-1,3-diene 
• 80-62-6 methacrylic acid methyl ester 
• 6493-77-2 methyl cyclohex-3-ene-1-carboxylate 
• 74-88-4 methyl iodide 

Downstream Products

• 825-04-7 methyl 1-methylcyclohexanecarboxylate 
• 50552-10-8 1-Hydroxymethyl-1-methyl-cyclohex-3-en 
• 91138-78-2 1-(α-Chlor-isopropyl)-1-methyl-cyclohexan 
• 699-42-3 1-methyl-2,4-cyclohexadienecarbonsaeure-methylester 
• 14064-13-2 (1-methylcyclohexyl)methanol 
• 27331-02-8 2-(1-methyl-cyclohexyl)-propan-2-ol 
• 90976-68-4 1-(α-Chlor-isopropyl)-1-methyl-cyclohex-3-en 
• 931-96-4 1-methyl-3-cyclohexene-1-carboxaldehyde 
• 50552-14-2 4-Methyl-4-nitrosooxymethyl-cyclohexene 
• 85319-31-9 Toluene-4-sulfonic acid (1R,5R)-5-methyl-6-oxo-bicyclo[3.2.1]oct-1-yl ester 
• 85319-28-4 [2-(1-Methyl-3-oxo-cyclohexyl)-2-oxo-ethyl]-phosphonic acid dimethyl ester 
• 344332-94-1 1-(3-Hydroxy-1-methyl-cyclohexyl)-2-methanesulfonyl-ethanone 
• 85319-23-9 3-(2-Methanesulfonyl-acetyl)-3-methyl-cyclohexanone 
• 87787-20-0 2-[4-Methyl-4-(4-nitro-phenoxymethyl)-cyclohexyloxy]-tetrahydro-pyran 

Relevant academic research and scientific papers

New entry to the enantioselective formation of substituted cyclohexenes bearing an all-carbon quaternary stereogenic center

Enantioselective formation of cyclohexene derivatives bearing an all-carbon quaternary stereogenic center is described. The racemic cyclohexenes are readily transformed to chiral substituted cyclohexenes in good yield with excellent enantioselectivity and diastereoselectivity by a palladium-mediated deracemization. The resulting products are promising synthetic intermediates of biologically active natural products. This protocol provides us with a new entry to the concise and scalable synthesis of multifunctionalized compounds.

Studies towards the synthesis of coprinolone, Δ6- coprinolone, and radulone A via an anionic electrocyclization cascade

Studies towards the synthesis of coprinolone, Δ6- coprinolone, and radulone A, resulting in the synthesis of an advanced intermediate with the tricyclic protoilludane carbon skeleton, are described. Georg Thieme Verlag Stuttgart.

Enones with Strained Double Bonds. 8. The Bicyclooctane Systems

The bicyclic enones bicyclooct-1-en-3-one (4) and 1-methylbicyclooct-5(6)-en-7-one (5) have been generated from various precursors and trapped by the addition of nucleophiles such as MeOH, PhSeH, or H2O.The bridgehead enone 5 has also been trapped as its cycloadduct 31 with furan.Pyrolysis of this cycloadduct 31 reformed the bridgehead enone 5 that was trapped as the cycloadduct 32.Related bridgehead enones 35 and 47 have also been generated as intermediates leading to products with bridgehead methoxy substituents.