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Chemical Structure| 301-02-0 Chemical Structure| 301-02-0
Chemical Structure| 301-02-0

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Oleamide is an endogenous fatty acid amide synthesized de novo in the mammalian nervous system and detected in human plasma.

Synonyms: cis-9-Octadecenamide

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Details of Oleamide

CAS No. :301-02-0
Formula : C18H35NO
M.W : 281.48
SMILES Code : CCCCCCCC/C=C\CCCCCCCC(N)=O
Synonyms :
cis-9-Octadecenamide
English Name :(9Z)-9-Octadecenamide
MDL No. :MFCD00053638

Safety of Oleamide

Application In Synthesis of Oleamide

* 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 [ 301-02-0 ]

[ 301-02-0 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 3999-01-7 ]
  • [ 301-02-0 ]
YieldReaction ConditionsOperation in experiment
95% With ammonia In dichloromethane for 1h; Ambient temperature;
  • 2
  • [ 301-02-0 ]
  • [ 1323108-64-0 ]
  • [ 629-54-9 ]
  • [ 124-26-5 ]
  • [ 112-69-6 ]
  • [ 124-28-7 ]
  • [ 1323108-61-7 ]
  • [ 14727-68-5 ]
  • 3
  • [ 124-40-3 ]
  • [ 2733-91-7 ]
  • [ 301-02-0 ]
  • [ 1323108-64-0 ]
  • [ 629-54-9 ]
  • [ 124-26-5 ]
  • 4
  • [ 1196-92-5 ]
  • [ 301-02-0 ]
  • [ 58493-49-5 ]
YieldReaction ConditionsOperation in experiment
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In N,N-dimethyl-formamide at 20℃; for 15h;
  • 5
  • [ 301-02-0 ]
  • [ 100-46-9 ]
  • [ 101762-87-2 ]
YieldReaction ConditionsOperation in experiment
90% With Ce(III) immobilised on an aminated epichlorohydrin-activated agarose matrix at 140℃; for 25h; Green chemistry; General procedure for transamidation of benzamide with benzylamine using CAEA and recovery of CAEA General procedure: CAEA (0.01 g) was added to a mixture of benzamide (1 mmol, 0.121 g) and benzylamine (1.1 mmol, 0.117 g) in a round-bottom flask equipped with a condenser under solvent-free conditions. The reaction mixture was stirred (250 min-1) at 140 °C. The progress of the reaction was monitored by TLC. Following the reaction, the reaction mixture was cooled and the resultant mixture was submitted to silica gel preparative TLC using ethyl acetate/hexane (1/1) as eluent. N-Benzylbenzamide was obtained with a 95 % yield (0.198 g). The spectral data of the compounds are given in Tables 1 and 2. The reaction mixture was centrifuged (1000 min-1,10 min) and washed several times with ethyl acetate and acetone to remove all the organic compounds then the precipitate was dried at ambient temperature.
 

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