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trans-4-Methylcyclohexanecarboxylic acid

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trans-4-Methylcyclohexanecarboxylic acid Basic information

Product Name:
trans-4-Methylcyclohexanecarboxylic acid
Synonyms:
  • trans-4-Methyl-1-cyclohexanecarboxylic acid 98%
  • trans-4-Methylcyclohexanecarboxylic Acid
  • Tranexamic Acid Impurity 3
  • TRANS-4-METHYL HEXAHYDROBENZOIC ACID
  • TRANS-4-METHYLCYCLOHEXANECARBOXYLIC ACID
  • trans-4-Methyl-1-cyclohexanecarboxylic acid
  • 4-methylcyclohexane-1-carboxylic acid
  • Cyclohexanecarboxylic acid, 4-methyl-, trans-
CAS:
13064-83-0
MF:
C8H14O2
MW:
142.2
EINECS:
235-959-6
Product Categories:
  • Biphenyl & Diphenyl ether
  • (intermediate of glimepiride)
  • 4-Alkylcyclohexanecarboxylic Acids (Building Blocks for Liquid Crystals)
  • 4-Substituted Cyclohexanecarboxylic Acids
  • Building Blocks for Liquid Crystals
  • Functional Materials
  • C8
  • Carbonyl Compounds
  • Carboxylic Acids
  • Building Blocks
  • Carbonyl Compounds
  • Carboxylic Acids
  • Chemical Synthesis
  • Organic Building Blocks
Mol File:
13064-83-0.mol
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trans-4-Methylcyclohexanecarboxylic acid Chemical Properties

Melting point:
109-111 °C (lit.)
Boiling point:
245 °C
Density 
1.025±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
pka
pK1:4.89 (25°C)
color 
White to Almost white
InChI
InChI=1S/C8H14O2/c1-6-2-4-7(5-3-6)8(9)10/h6-7H,2-5H2,1H3,(H,9,10)/t6-,7-
InChIKey
QTDXSEZXAPHVBI-LJGSYFOKSA-N
SMILES
[C@@H]1(C(O)=O)CC[C@@H](C)CC1
CAS DataBase Reference
13064-83-0(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
24/25
WGK Germany 
3
HS Code 
29162090

MSDS

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trans-4-Methylcyclohexanecarboxylic acid Usage And Synthesis

Chemical Properties

White crystal

Uses

trans-4-Methyl-1-cyclohexanecarboxylic acid may be used in chemical synthesis.

Synthesis

99-94-5

934-67-8

934-67-8

General procedure: The hydrogenation reaction is carried out in a 25 mL stainless steel autoclave with a PTFE liner. Typical operation is as follows: 20 mg of catalyst and 61 mg (0.5 mmol) of p-toluic acid are dispersed homogeneously 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. The reaction system was heated to 110 °C under magnetic stirring (1000 rpm) and maintained until the reaction was completed. At the end of the reaction, the mixture was extracted using ethyl acetate and the solid catalyst was removed by centrifugation. 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 subjected to structural confirmation 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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