4342-60-3

Usage

Uses

Used in Perfumery Industry:
4-METHYL-3-CYCLOHEXENE-1-CARBOXYLIC ACID is used as a fragrance ingredient for its ability to mimic the scent of cumin oil and/or cumene aldehyde. It is particularly suitable for use in perfumes that are applied to fabric softeners, cleaning compounds, shampoos, and other personal care products.
Used in Cleaning Compounds:
In the cleaning industry, 4-METHYL-3-CYCLOHEXENE-1-CARBOXYLIC ACID serves as a replacement for cumin oil and/or cumene aldehyde, providing a pleasant scent to cleaning products without the need for more expensive or less stable ingredients.
Used in Fabric Softeners:
4-METHYL-3-CYCLOHEXENE-1-CARBOXYLIC ACID is used as a scent enhancer in fabric softeners, imparting a fresh and appealing fragrance to laundered fabrics.
Used in Shampoos:
In the personal care industry, 4-METHYL-3-CYCLOHEXENE-1-CARBOXYLIC ACID is used in shampoos to provide a pleasant scent and improve the overall sensory experience of hair washing.
Used in Aromatherapy:
4-METHYL-3-CYCLOHEXENE-1-CARBOXYLIC ACID may also find use in aromatherapy products, where its unique scent can contribute to creating a relaxing or invigorating atmosphere.

InChI:InChI=1/C8H12O2/c1-6-2-4-7(5-3-6)8(9)10/h2,7H,3-5H2,1H3,(H,9,10)

Upstream product

• 6090-09-1 (+-)-4-acetyl-1-methylcyclohexene 
• 586-30-1 3-hydroxy-4-methylbenzoic acid 
• 937-28-0 4c-hydroxy-4t-methyl-cyclohexane-r-carboxylic acid 
• 90113-41-0 4-hydroxy-4-methylcyclohexane-1-carboxylic acid 
• 1120-56-5 methylidenecyclobutane 
• 79-10-7 acrylic acid 
• 78-79-5 isoprene 
• 71-43-2 benzene 
• 20292-15-3 4-methyl-cyclohex-3-enecarboxylic acid ethyl ester 
• 2698-65-9 4-methylcyclohex-3-ene-1,1-dicarboxylic acid diethyl ester 
• 7560-64-7 4-methyl-cyclohex-3-enecarbaldehyde 
• 99380-79-7 3,3,9-Trimethyl-2,4-dioxa-spiro[5.5]undec-8-ene-1,5-dione 
• 6493-79-4 methyl 4-methyl-3-cyclohexene-1-carboxylate 
• 19900-46-0 acrylic acid-(β,γ-epoxy-isobutyl ester) 

Downstream Products

• 20292-15-3 4-methyl-cyclohex-3-enecarboxylic acid ethyl ester 
• 54385-26-1 4-Methyl-N-methyl-3-cyclohexencarboxamid 
• 117015-88-0 (3R,4R)-4-Bromo-3-methoxy-3-methyl-cyclohexanecarboxylic acid methyl ester 
• 115664-07-8 3-Brom-4-methoxy-4-methyl-cyclohexan-1-carbonsaeuremethylester 
• 152668-10-5 1-(4-Chlorobutyl)-4-methyl-3-cyclohexenecarboxylic acid 
• 94294-81-2 (1R*,1R*)-1-(1,5-dimethyl-1-hydroxy-4-hexene)-4-methyl-3-cyclohexenecarboxylic acid 
• 94294-79-8 (1S*,1R*)-1-(1,5-dimethyl-1-hydroxy-4-hexene)-4-methyl-3-cyclohexenecarboxylic acid 
• 119908-42-8 1-((R)-4-Methyl-cyclohex-3-enecarbonyl)-1,3-bis-((S)-1-phenyl-ethyl)-urea 
• 104762-26-7 (2-methyl-1-cyclopentenyl)methyl 4-methyl-3-cyclohexene-1-carboxylate 
• 100231-41-2 4-Methyl-cyclohex-3-enecarboxylic acid 2-methoxy-3-methyl-cyclopent-2-enyl ester 
• 79743-47-8 cis-4,trans-3-dichloro-4-methylcyclohexanecarboxylic acid 
• 16695-95-7 (4'-methylcyclohex-3'-ene-1-'-yl)carbonyl chloride 
• 26034-64-0 4-methyl-cyclohex-3-enecarboxylic acid 4-(3-cyclohexyl-2-imino-imidazolidine-1-sulfonyl)-phenethylamide 
• 147118-84-1 4-methyl-cis-4-phenylcyclohexanecarboxylic acid 

Relevant academic research and scientific papers

TWO CONVENIENT METHODS FOR THE GENERATION OF "METHYLENE MELDRUM'S ACID" FOR DIELS- ALDER REACTIONS.

The transient isopropylidene methylenemalonate can be easily generated by treating either Meldrum's acid or diisopropylidene methylenedimalonate with formaldehyde, and trapped by reactive dienes.

CANNABINOID DERIVATIVES, PRECURSORS AND USES

The present disclosure relates to new cannabinoid derivatives and precursors and processes for their preparation. The disclosure also relates to pharmaceutical and analytical uses of the new cannabinoid derivatives.

METHODS OF SYNTHESIS OF (1R,2R,5R)-5-AMINO-2-METHYLCYCLOHEXANOL HYDROCHLORIDE AND INTERMEDIATES USEFUL THEREIN

Provided herein are methods and intermediates for making (lR,2R,5R)-5-amino-2- methylcyclohexanol hydrochloride, which are useful for the preparation of compounds useful for the treatment of a disease, disorder, or condition associated with the JNK pathwa

BORON-BASED CYCLOADDITION CATALYSTS AND METHODS FOR THE PRODUCTION OF BIO-BASED TEREPHTHALIC ACID, ISOPHTHALIC ACID AND POLY (ETHYLENE TEREPHTHALATE)

Methods for producing cycloaddition products comprising: reacting a diene with a dienophile in the presence of one or more boron-based catalysts of Formula I or Formula II are provided. In particular, the methods can be used to prepare 4-methyl-3-cyclohexene- 1-carboxylic acid and 3-methyl-3-cyclohexene-l-carboxylic acid, including bio-based versions thereof. The cycloaddition products can be advantageously used in the production of terephthalic acid and isophthalic acid, and ultimately, poly(ethylene terephthalate), and bio-based versions thereof. Formula I Formula II

Method for preparation of 4-methylcyclohex-3-ene-1-carboxylic acid from 4-methyl-3-cyclohexene-1-carbaldehyde

The invention relates to a method for preparation of 4-methylcyclohex-3-ene-1-carboxylic acid by selective oxidation of 4-methyl-3-cyclohexene-1-carbaldehyde. Specifically, the method includes: under an alkaline condition, under the action of a supported

Polyelectrolyte-catalyzed Diels–Alder reactions

Imidazolium-based poly(ionic liquids) bearing bromide and bis(trifluoromethane)sulfonimide as counteranions [poly(ViEIm)Br and poly(ViEIm)NTf2] derived from reversible addition fragmentation chain transfer (RAFT) polymerization techniques are u

Synthesis of 1,3-Cycloalkadienes from Cycloalkenes: Unprecedented Reactivity of Oxoammonium Salts

Few methods allow for the direct conversion of cycloalkenes into cycloalkadienes with high chemo- and regioselectivity. Herein, we report a convenient one-pot process for this transformation that involves the unprecedented N-preferential group transfer of N-oxoammonium salts to cycloalkenes, followed by Cope elimination, to afford cycloalkadienes at room temperature and pressure.

NOVEL COMPOUNDS

Novel rapamycin analogues and methods for their production with FKBP and/or MIP inhibitory activity with reduced mTOR inhibitory activity with therapeutic potential e.g. as bacterial virulence inhibitors.

SOLID FORMS OF 2-(TERT-BUTYLAMINO)-4-((1R,3R,4R)-3-HYDROXY-4-METHYLCYCLOHEXYLAMINO)-PYRIMIDINE-5-CARBOXAMIDE, COMPOSITIONS THEREOF AND METHODS OF THEIR USE

Provided herein are formulations, processes, solid forms and methods of use relating to 2- (tert-butylamino)-4-((lR,3R,4R)-3-hydroxy-4-methylcyclohexylamino)-pyrimidine-5- carboxamide.

Dehydro-aromatization of cyclohexene-carboxylic acids by sulfuric acid: Critical route for bio-based terephthalic acid synthesis

A novel dehydro-aromatization reaction under mild reaction conditions was successfully developed using sulfuric acid as a cost-effective and efficient oxidant. This reaction simplified the synthesis of terephthalic acid (TA, an important aromatic monomer precursor) from biomass-derived isoprene and acrylic acid.