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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
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Chemical Structure| 4630-82-4 Chemical Structure| 4630-82-4
Chemical Structure| 4630-82-4

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Methyl Cyclohexanecarboxylate is an endogenous metabolite.

4.5 *For Research Use Only !

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Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

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Product Details of Methyl cyclohexanecarboxylate

CAS No. :4630-82-4
Formula : C8H14O2
M.W : 142.19
SMILES Code : COC(=O)C1CCCCC1
MDL No. :MFCD00001458
InChI Key :ZQWPRMPSCMSAJU-UHFFFAOYSA-N
Pubchem ID :20748

Safety of Methyl cyclohexanecarboxylate

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225
Precautionary Statements:P210-P403+P235
Class:3
UN#:3272
Packing Group:

Application In Synthesis of Methyl cyclohexanecarboxylate

* 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 [ 4630-82-4 ]

[ 4630-82-4 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 67-56-1 ]
  • [ 70264-96-9 ]
  • [ 4630-82-4 ]
  • [ 6642-30-4 ]
  • [ 71099-00-8 ]
  • 2
  • [ 4630-82-4 ]
  • [ 12012-95-2 ]
  • [ 75266-48-7 ]
  • 3
  • [ 4630-82-4 ]
  • [ 12012-95-2 ]
  • [ 138052-81-0 ]
  • 4
  • [ 4630-82-4 ]
  • [ 103347-14-4 ]
  • methyl1-(4-chloro-3-methoxybenzyl)cyclohexanecarboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
n-Butyllithium (2.5 M in hexanes) (6.06 ml, 15.2 mmol) was addeddropwise to a -78 oc solution of diisopropylamine (2.16 ml, 15.2 mmol) in tetrahydrofuran(THF) (40 ml). The mixture was allowed to warm to room temperature and stirred for 15minutes. The mixture was cooled to -78 oc before methyl cyclohexanecarboxylate (2.06ml, 14.4 mmol) was added dropwise. The mixture was warmed to 0 oc and stirred for 15minutes. A solution of <strong>[103347-14-4]4-(bromomethyl)-1-chloro-2-methoxybenzene</strong> (1.7 g, 7.22 mmol) intetrahydrofuran (THF) (13.3 ml) was added dropwise. The mixture was stirred anadditional 20 minutes at 0 oc and then quenched with saturated ammonium chloride. Themixture was extracted 2 times with ethyl acetate. The combined organic layers werewashed with brine, dried over sodium suflate, and concentrated to give crude methyl 1-(4-chloro-3-methoxybenzyl)cyclohexane-1-carboxylate (2.14 g). 1H NMR (400 MHz,CHLOROFORM-d) o ppm 7.15-7.28 (m, 1 H), 6.51-6.62 (m, 2 H), 3.84 (s, 3 H), 3.60 (s, 3H), 2.74 (s, 2 H), 1.36-2.09 (m, 4 H), 1.12- 1.34 (m, 6 H).
 

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