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Chemical Structure| 712-09-4 Chemical Structure| 712-09-4
Chemical Structure| 712-09-4

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5-Methoxytryptophol is a naturally occurring indole compound in the pineal gland, a metabolite of melatonin.

Synonyms: 5-MTOH

4.5 *For Research Use Only !

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Product Details of 5-Methoxytryptophol

CAS No. :712-09-4
Formula : C11H13NO2
M.W : 191.23
SMILES Code : COC1=CC2=C(NC=C2CCO)C=C1
Synonyms :
5-MTOH
MDL No. :MFCD00047196
InChI Key :QLWKTGDEPLRFAT-UHFFFAOYSA-N
Pubchem ID :12835

Safety of 5-Methoxytryptophol

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H317
Precautionary Statements:P280

Application In Synthesis of 5-Methoxytryptophol

* 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 [ 712-09-4 ]

[ 712-09-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3471-31-6 ]
  • [ 712-09-4 ]
YieldReaction ConditionsOperation in experiment
In tetrahydrofuran; diethyl ether; Stage 1 2-(5-Methoxyindol-3-yl)ethanol A solution of 15 g of (5-methoxyindol-3-yl)acetic acid (0.073 mol) in 100 ml of tetrahydrofuran is added to a suspension of 2.1 g (0.219 mol) of lithium aluminum hydride in 100 ml of ethyl ether and the reaction mixture is brought to reflux for 6 hours. The reaction mixture is then hydrolyzed with 80 ml of a saturated aqueous magnesium sulfate solution. The whole mixture is filtered through celite and the solvents are evaporated under vacuum. The residue is taken up in a small amount of water and extracted a number of times with dichloromethane. The product is obtained after evaporation of the solvant.
 

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