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Chemical Structure| 5292-21-7 Chemical Structure| 5292-21-7
Chemical Structure| 5292-21-7

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Cyclohexaneacetic acid is a flavouring ingredient.

4.5 *For Research Use Only !

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Product Details of Cyclohexaneacetic acid

CAS No. :5292-21-7
Formula : C8H14O2
M.W : 142.20
SMILES Code : O=C(O)CC1CCCCC1
MDL No. :MFCD00001518
InChI Key :LJOODBDWMQKMFB-UHFFFAOYSA-N
Pubchem ID :21363

Safety of Cyclohexaneacetic acid

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of Cyclohexaneacetic acid

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 5292-21-7 ]

[ 5292-21-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1189-71-5 ]
  • [ 5292-21-7 ]
  • [ 4435-14-7 ]
YieldReaction ConditionsOperation in experiment
14.6 g (85%) In dichloromethane; N,N-dimethyl-formamide; Step (1) Preparation of Cyclohexylacetonitrile A solution of the cyclohexylacetic acid (20.0 g, 141 mmol) in CH2 Cl2 (80 mL) was heated to reflux and a solution of chlorosulfonyl isocyanate (20.9 g, 148 mmol) in CH2 Cl2 (18 mL) was added dropwise over 40 minutes. After the addition was complete, stirring was continued at reflux for 65 minutes. The mixture was cooled to 0 C., and DMF (21.1 g, 288 mmol) was added dropwise. The mixture was allowed to warm to room temperature and stirred 18 hours. The mixture was poured over ice, the organic layer separated, and the aqueous layer extracted with CH2 Cl2 (50 mL). The combined organic layers were washed with water (3*50 mL), brine, dried (Na2 SO4), filtered through a plug of Florosil and concentrated. The nitrile was obtained as 14.6 g (85%) of an oil of sufficient purity for use in the next reaction. NMR (DMSO-d6, 200 MHz): delta 1.10 (m, 5H), 1.62 (m, 6H), 2.40 (d, J=7.0, 2H).
  • 2
  • [ 5292-21-7 ]
  • [ 4435-14-7 ]
 

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