Basic information Safety Supplier Related

4-Methylcyclohexanecarboxylic acid

Basic information Safety Supplier Related

4-Methylcyclohexanecarboxylic acid Basic information

Product Name:
4-Methylcyclohexanecarboxylic acid
Synonyms:
  • 4-METHYL-CYCLOHEXANECARBOXYLIC ACID
  • 4-METHYL-1-CYCLOHEXANECARBOXYLIC ACID
  • 4-Methyl-1-cyclohexanecarboxylic acid,mixture of cis and trans
  • 4-METHYL-1-CYCLOHEXANECARBOXYLIC ACID, 9 9%, MIXTURE OF CIS AND TRANS
  • 4-Methyl-1-cyclohexanecarboxylic acid, 98%, mixture of cis and trans
  • 4-Methylcyclohexanecarboxylic Acid (cis- and trans- mixture)
  • 4-METHYL-1-CYCLOHEXANECARBOXYLICACID(CIS+TRANS)
  • trans-4-Methyl-1-cyclohexanecarboxylic acid
CAS:
4331-54-8
MF:
C8H14O2
MW:
142.2
EINECS:
224-369-4
Product Categories:
  • Building Blocks
  • Carbonyl Compounds
  • Carboxylic Acids
  • Chemical Synthesis
  • Organic Building Blocks
  • 4-Alkylcyclohexanecarboxylic Acids (Building Blocks for Liquid Crystals)
  • 4-Substituted Cyclohexanecarboxylic Acids
  • Building Blocks for Liquid Crystals
  • Functional Materials
  • C8
  • Carbonyl Compounds
  • Carboxylic Acids
Mol File:
4331-54-8.mol
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4-Methylcyclohexanecarboxylic acid Chemical Properties

Melting point:
110 °C
Boiling point:
134-136 °C/15 mmHg (lit.)
Density 
1.005 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.4598(lit.)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform, DMSO, Methanol
pka
4.92±0.10(Predicted)
form 
Oil
color 
Clear Colorless
InChI
InChI=1S/C8H14O2/c1-6-2-4-7(5-3-6)8(9)10/h6-7H,2-5H2,1H3,(H,9,10)
InChIKey
QTDXSEZXAPHVBI-UHFFFAOYSA-N
SMILES
C1(C(O)=O)CCC(C)CC1
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36
Safety Statements 
26
WGK Germany 
2
HS Code 
29162090

MSDS

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4-Methylcyclohexanecarboxylic acid Usage And Synthesis

Chemical Properties

Relative density 1.005, melting point 108-111°C, boiling point 134-136°C (15mmHg), refractive index 1.4598.

Uses

4-Methyl-1-cyclohexanecarboxylic acid was used to investigate the palladium core-porous silica shell-nanoparticles catalyzed hydrogenation of 4-carboxybenzaldehyde (4-CBA) to p-toluic acid. It was also used in the synthesis of substituted cyclohexyl carbonyl chlorides.

Synthesis

99-94-5

934-67-8

934-67-8

GENERAL STEPS: The hydrogenation reaction was carried out in a 25 mL stainless steel autoclave with a PTFE liner. In a typical experiment, 20 mg of catalyst and 61 mg (0.5 mmol) of p-toluic acid were dispersed in 5 mL of deionized water. After sealing the autoclave, the air in the autoclave was replaced with hydrogen and pressurized to 2.5 MPa. Subsequently, the reaction mixture was heated to 110 °C under magnetic stirring (1000 rpm). Upon completion of the reaction, it was cooled to room temperature, the reaction mixture was extracted with ethyl acetate and separated by centrifugation to remove the solid catalyst. The recovered solid catalyst was washed sequentially with ethyl acetate, ethanol and deionized water. The filtrate was analyzed by gas chromatography (GC, HP5890, USA) equipped with a 30 m HP-5 capillary column and a flame ionization detector (FID). All products were confirmed structurally by gas chromatography-mass spectrometry (GC-MS, Agilent 6890).

References

[1] Tetrahedron Letters, 2004, vol. 45, # 35, p. 6669 - 6672
[2] Steroids, 1983, vol. 41, # 3, p. 349 - 359
[3] Recueil des Travaux Chimiques des Pays-Bas, 1961, vol. 80, p. 595 - 607
[4] Recueil des Travaux Chimiques des Pays-Bas, 1961, vol. 80, p. 595 - 607
[5] Journal of the Chemical Society, 1937, p. 2003,2007

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