ChemicalBook--->CAS DataBase List--->13064-83-0

13064-83-0

13064-83-0 Structure

13064-83-0 Structure
IdentificationMore
[Name]

trans-4-Methylcyclohexanecarboxylic acid
[CAS]

13064-83-0
[Synonyms]

TRANS-4-METHYL-1-CYCLOHEXANECARBOXYLIC ACID
TRANS-4-METHYLCYCLOHEXANECARBOXYLIC ACID
TRANS-4-METHYL HEXAHYDROBENZOIC ACID
[EINECS(EC#)]

235-959-6
[Molecular Formula]

C8H14O2
[MDL Number]

MFCD00074943
[Molecular Weight]

142.2
[MOL File]

13064-83-0.mol
Chemical PropertiesBack Directory
[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)
Safety DataBack Directory
[Risk Statements ]

36/37/38
[Safety Statements ]

24/25
[WGK Germany ]

3
[HS Code ]

29162090
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

White crystal
[Uses]

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

p-Toluic acid

99-94-5

cis-4-methylcyclohexanecarboxylic acid

934-67-8

cis-4-methylcyclohexanecarboxylic acid

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
Spectrum DetailBack Directory
[Spectrum Detail]

trans-4-Methylcyclohexanecarboxylic acid(13064-83-0)1HNMR
trans-4-Methylcyclohexanecarboxylic acid(13064-83-0)IR
trans-4-Methylcyclohexanecarboxylic acid(13064-83-0)Raman
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

trans-4-Methyl-1-cyclohexanecarboxylic acid, 98%(13064-83-0)
[Sigma Aldrich]

13064-83-0(sigmaaldrich)
[TCI AMERICA]

trans-4-Methylcyclohexanecarboxylic Acid,>98.0%(GC)(T)(13064-83-0)
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