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Chemical Structure| 73-31-4 Chemical Structure| 73-31-4
Chemical Structure| 73-31-4

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Melatonin is a hormone which plays a role in natural sleep-wake cycle and also a ATF6 blocker.

Synonyms: N-Acetyl-5-methoxytryptamine; NSC 56423; 5-Methoxy-N-acetyltryptamine

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Product Details of Melatonin

CAS No. :73-31-4
Formula : C13H16N2O2
M.W : 232.28
SMILES Code : COC1=CC2=C(NC=C2CCNC(C)=O)C=C1
Synonyms :
N-Acetyl-5-methoxytryptamine; NSC 56423; 5-Methoxy-N-acetyltryptamine
MDL No. :MFCD00005655
InChI Key :DRLFMBDRBRZALE-UHFFFAOYSA-N
Pubchem ID :896

Safety of Melatonin

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of Melatonin

* 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 [ 73-31-4 ]

[ 73-31-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 73-31-4 ]
  • [ 802919-90-0 ]
  • [ 1609470-74-7 ]
  • 2
  • [ 73-31-4 ]
  • [ 4263-52-9 ]
  • C15H19N2O5S(1-)*Na(1+) [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate; In acetonitrile; at 80℃; 100 mg of melatonin was dissolved in 10 mL of acetonitrile, and then 137 mg of sodium carbonate and 136 mg of sodium bromoethylsulfonate were added, and the reaction was stirred at 80C overnight. After the end of the reaction, the residue obtained by spin-drying is separated and purified by column chromatography to obtain the target molecule 2, and the reaction formula is as follows:
 

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