4342-60-3

Basic information

• Product Name: 4-Methyl-3-cyclohexene-1-carboxylic Acid
• Synonyms: 4-Methyl-3-cyclohexene-1-carboxylic Acid;4-Methylcyclohex-3-ene-1-carboxylicacid;4-Methylcyclohex-3-Ene-1-Carboxylic Acid(WX610371)
• CAS NO: 4342-60-3
• Molecular Formula: C₈H₁₂O₂
• Molecular Weight: 140.17968
• Mol File: 4342-60-3.mol
• Article Data: 19

Chemical Properties

• Melting Point: 98.0 to 102.0 °C
• Boiling Point: 251.4°C at 760 mmHg
• Flash Point: 116.5°C
• Appearance: /
• Density: 1.078g/cm³
• Vapor Pressure: 0.00644mmHg at 25°C
• Refractive Index: 1.497
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 4.68±0.40(Predicted)
• CAS DataBase Reference: 4-Methyl-3-cyclohexene-1-carboxylic Acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Methyl-3-cyclohexene-1-carboxylic Acid(4342-60-3)
• EPA Substance Registry System: 4-Methyl-3-cyclohexene-1-carboxylic Acid(4342-60-3)

Safety Data

• Hazardous Substances Data: 4342-60-3(Hazardous Substances Data)

Usage

Uses

4-Methylcyclohex-3-ene-1-carboxylic acid is useful as a replacement for cumin oil and/or cumene aldehyde in perfumes used with fabric softeners, cleaning compounds, shampoos e.t.c

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

• 937-28-0 4c-hydroxy-4t-methyl-cyclohexane-r-carboxylic acid 
• 937-28-0 4t-hydroxy-4c-methyl-cyclohexane-r-carboxylic acid 
• 90113-41-0 4-hydroxy-4-methylcyclohexane-1-carboxylic acid 
• 79-10-7 acrylic acid 
• 78-79-5 isoprene 
• 1120-56-5 methylidenecyclobutane 
• 71-43-2 benzene 
• 7560-64-7 4-methyl-cyclohex-3-enecarbaldehyde 
• 6493-79-4 methyl 4-methyl-3-cyclohexene-1-carboxylate 
• 19900-46-0 acrylic acid-(β,γ-epoxy-isobutyl ester) 
• 151153-99-0 3-[(4'-methylcyclohex-3'-ene-1'-yl)carbonyl]oxazolidin-2-one 
• 874-61-3 4-oxocyclohexanecarboxylic acid 
• 90113-39-6 3-hydroxy-4-methyl-cyclohexanecarboxylic acid 
• 932-00-3 1-methyl-2-oxabicyclo[2.2.2]octane 

Downstream Products

• 20292-15-3 4-methyl-cyclohex-3-enecarboxylic acid ethyl ester 
• 94294-79-8 (1S*,1R*)-1-(1,5-dimethyl-1-hydroxy-4-hexene)-4-methyl-3-cyclohexenecarboxylic acid 
• 39155-38-9 (4-methylcyclohex-3-en-1-yl)methanol 
• 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 
• 94294-81-2 (1R*,1R*)-1-(1,5-dimethyl-1-hydroxy-4-hexene)-4-methyl-3-cyclohexenecarboxylic acid 
• 92730-88-6 3-Oxo-2-aethoxycarbonyl-3-(4-methyl-cyclohexen-⁽³⁾-yl)-propionsaeure-aethylester 
• 859179-02-5 3,4-dibromo-4-methyl-cyclohexanecarboxylic acid 
• 622793-07-1 1-(1-hydroxy-1,5-dimethylhex-5-enyl)-4-methylcyclohex-3-enecarboxylic acid 
• 496808-23-2 4-[(E/Z)-1,5-dimethylhex-5-enylidene]-1-methylcyclohex-1-ene 
• 104762-31-4 1-(hydroxymethyl)-4-methyl-1-(1-methyl-2-methylenecyclopentyl)-3-cyclohexene 
• 104762-29-0 methyl 4-methyl-1-(1-methyl-2-methylenecyclopentyl)-3-cyclohexene-1-carboxylate 
• 100231-45-6 1-(2-Methoxy-1-methyl-cyclopent-2-enyl)-4-methyl-cyclohex-3-enecarboxylic acid 

Relevant articles and documents

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.

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

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