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Chemical Structure| 3943-97-3 Chemical Structure| 3943-97-3
Chemical Structure| 3943-97-3

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Methyl p-coumarate (Methyl 4-hydroxycinnamate) is a derivative of coumaric acid that can inhibit melanin formation and the growth of various pathogens.

Synonyms: Methyl 4-hydroxycinnamate

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Product Details of Methyl p-coumarate

CAS No. :3943-97-3
Formula : C10H10O3
M.W : 178.18
SMILES Code : O=C(OC)/C=C/C1=CC=C(O)C=C1
Synonyms :
Methyl 4-hydroxycinnamate
MDL No. :MFCD00157167

Safety of Methyl p-coumarate

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of Methyl p-coumarate

* 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 [ 3943-97-3 ]

[ 3943-97-3 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 3943-97-3 ]
  • [ 3101-60-8 ]
  • [ 70193-89-4 ]
  • 2
  • [ 3943-97-3 ]
  • [ 3101-60-8 ]
  • [ 60377-18-6 ]
  • 3
  • [ 67-56-1 ]
  • genistein 7-O-(2"-p-coumaroyl-β-D-glucopyranoside) [ No CAS ]
  • [ 3943-97-3 ]
  • [ 529-59-9 ]
  • 4
  • [ 3943-97-3 ]
  • [ 14704-31-5 ]
  • C23H20O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N,N-dimethyl-formamide; at 50℃; for 6h;Inert atmosphere; General procedure: To a mixture of compound 2 (550?mg, 2.0?mmol), methyl-4-hydroxycinnamate (434?mg, 2.3?mmol) in DMF (10.0?mL) was added K2CO3 (1.38?g, 10.0?mmol) and the mixture was stirred for 6?h?at 50?C. After cooling, the resulting mixture was extracted with EtOAc and water. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography (hexane/EtOAc?=?15/1) to afford compound 7b (457?mg, 63.8%) as a white solid.
  • 5
  • [ 3943-97-3 ]
  • [ 1700-31-8 ]
  • C24H22O4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N,N-dimethyl-formamide; at 50℃; for 6h;Inert atmosphere; General procedure: To a mixture of compound 2 (550?mg, 2.0?mmol), methyl-4-hydroxycinnamate (434?mg, 2.3?mmol) in DMF (10.0?mL) was added K2CO3 (1.38?g, 10.0?mmol) and the mixture was stirred for 6?h?at 50?°C. After cooling, the resulting mixture was extracted with EtOAc and water. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography (hexane/EtOAc?=?15/1) to afford compound 7b (457?mg, 63.8percent) as a white solid.
  • 6
  • [ 3943-97-3 ]
  • [ 3101-60-8 ]
  • [ 60377-55-1 ]
  • 7
  • [ 3943-97-3 ]
  • [ 17024-12-3 ]
  • C24H18O3 [ No CAS ]
 

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