39155-38-9

Usage

Uses

Used in Fragrance and Flavor Industry:
(4-methyl-3-cyclohexen-1-yl)methanol (SALTDATA: FREE) is used as a fragrance and flavoring agent for its strong, pleasant odor, enhancing the sensory experience of various consumer products.
Used in Perfume Production:
In the perfume industry, (4-methyl-3-cyclohexen-1-yl)methanol (SALTDATA: FREE) is used as a key ingredient to create unique and appealing scents, contributing to the overall composition and character of perfumes.
Used in Cosmetics and Personal Care Products:
(4-methyl-3-cyclohexen-1-yl)methanol (SALTDATA: FREE) is utilized in the formulation of cosmetics and personal care products, where its pleasant odor and other properties can improve the product's appeal and effectiveness.
Used as a Preservative:
Due to its antimicrobial properties, (4-methyl-3-cyclohexen-1-yl)methanol (SALTDATA: FREE) is used as a preservative in certain products to prevent microbial growth and extend shelf life.

InChI:InChI=1/C8H14O/c1-7-2-4-8(6-9)5-3-7/h2,8-9H,3-6H2,1H3

Upstream product

• 7560-64-7 4-methyl-cyclohex-3-enecarbaldehyde 
• 4342-60-3 4-methylcyclohex-3-enecarboxylic acid 
• 20292-15-3 4-methyl-cyclohex-3-enecarboxylic acid ethyl ester 
• 6493-79-4 methyl 4-methyl-3-cyclohexene-1-carboxylate 

Downstream Products

• 50552-15-3 1-Methyl-4-nitrosooxymethyl-cyclohexene 
• 3937-49-3 (trans-4-methylcyclohexyl)methanol 
• 3937-48-2 (cis-4-Methyl-cyclohexyl)-methanol 
• 7560-64-7 4-methyl-cyclohex-3-enecarbaldehyde 
• 53216-76-5 4-Methyl-3-cyclohexen-1-acetonitril 
• 7086-66-0 2-<(1RS)-4-methylcyclohex-3-enyl>acetic acid 
• 18240-10-3 (+/-)-2-(3-cyclohexenyl)ethanol 
• 744910-51-8 bis(4-methyl-3-cyclohexenylmethyl) succinate 
• 162132-42-5 (Z)-1-acetoxy-3-(4-methyl-3-cyclohexen-1-yl)-2-butene 
• 70286-15-6 methyl (Z)-3-(4-methyl-3-cyclohexen-1-yl)-2-butenoate 
• 162132-41-4 methyl 3-(4-methyl-3-cyclohexen-1-yl)propynoate 
• 162132-39-0 1,1-dibromo-2-(4-methyl-3-cyclohexen-1-yl)ethene 

Relevant academic research and scientific papers

Compound and preparation method and application thereof

The invention discloses a compound as well as a preparation method and application thereof, and the structural formula of the compound is as shown in formula 1. The research finds that the compound provided by the invention can be applied to preparation o

Simple, chemoselective hydrogenation with thermodynamic stereocontrol

Few methods permit the hydrogenation of alkenes to a thermodynamically favored configuration when steric effects dictate the alternative trajectory of hydrogen delivery. Dissolving metal reduction achieves this control, but with extremely low functional group tolerance. Here we demonstrate a catalytic hydrogenation of alkenes that affords the thermodynamic alkane products with remarkably broad functional group compatibility and rapid reaction rates at standard temperature and pressure.

Bis(phosphine)cobalt dialkyl complexes for directed catalytic alkene hydrogenation

Planar, low-spin cobalt(II) dialkyl complexes bearing bidentate phosphine ligands, (P - P)Co-(CH2SiMe3)2, are active for the hydrogenation of geminal and 1,2-disubstituted alkenes. Hydrogenation of more hindered internal and endocyclic trisubstituted alkenes was achieved through hydroxyl group activation, an approach that also enables directed hydrogenations to yield contrasteric isomers of cyclic alkanes.

Immobilization of macMillan imidazolidinone as mac-SILC and its catalytic performance on sustainable enantioselective dielsAlder cycloaddition

MacMillan's imidazolidinone catalyst was immobilized as a supported ionic liquid catalyst (Mac-SILC) in the pores of silica gel with the aid of an ionic liquid - 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide. The heterogenized organocatalyst was utilized for the enantioselective Diels-Alder reaction of cyclopentadiene and cinnamaldehyde, recovered by simple filtration and subsequent evacuation, and repeatedly used up to six times in 81% average chemical yield, 87% ee for endo- and 80% ee for exo-products. The Mac-SILC was effective for a variety of substrates.

Active ray curable ink-jet composition, image forming method using the same, ink-jet recording apparatus, and triarylsulfonium salt compound

An active ray curable ink-jet ink composition comprising a photo-induced acid generating agent containing an onium salt which does not generate benzene under active ray radiation, and a photopolymerizable compound containing a compound having an oxetane ring in the molecule.

131. Determination of the configuration of wine lactone

The intense sweet and coconut-like smelling odorant 1, named 'wine lactone', was isolated from different wine varieties. The chemical structure of this compound, which has not yet been detected in wine or a food, was identified by high-resolution mass spe

Termite trail attractants: New synthesis of racemic (E)-α-, (Z)-α- and β-bisabolenes

Racemic (E)-α-bisabolene (E)(1) was synthetized starting from 4-methyl-3-cyclohexenecarboxylic acid (3) by a reaction sequence involving the Pd(0)-catalyzed cross-coupling reaction between the (E)-2-methyl-1-alkenyltrimethylstannane 8 and 3-methyl-2-buten-1-yl acetate (9). Three different procedures, in which a common precursor was used as key intermediate, were tested for the synthesis of racemic (Z)-α-bisabolene (Z)(1). The best one, which involved the reaction between bromide 18 and lithium dialkenylcuprate 19, afforded a mixture of (Z)- and (E)-1 in a 93:7 molar ratio, respectively. Finally, racemic β-bisabolene (2) was synthetized by a simple reaction sequence involving the Zr-promoted methylenation of ketone 22 prepared from 3.