trans-4-Methylcyclohexanecarboxylic acid
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
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)
MSDS
- Language:English Provider:SigmaAldrich
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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trans-4-Methylcyclohexanecarboxylic acid(13064-83-0)Related Product Information
- Methyl salicylate
- Cyclohexanecarbonitrile
- Cyclohexanecarboxylic acid ethyl ester
- Cyclohexanecarboxylic acid
- Kresoxim-methyl
- p-Toluic acid
- Tribenuron methyl
- o-Toluic acid
- (Aminomethyl)cyclohexane
- Methyl acetate
- METSULFURON METHYL
- Tranexamic Acid
- BOC-N-METHYL-TRANEXAMIC ACID
- BOC-(4-AMINOMETHYL)-CYCLOHEXANE-CARBOXYLIC ACID
- Thiophanate-methyl
- Methyl
- cis,trans-(1,1-DiMethylethoxy)carbonyl TranexaMic Acid-13C2,15N
- trans-4-Propylcyclohexanecarboxylic acid