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Chemical Structure| 2199-90-8 Chemical Structure| 2199-90-8
Chemical Structure| 2199-90-8

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Ethyl 6-Bromocoumarin-3-carboxylate is a brominated coumarin derivative, commonly used in organic synthesis and fluorescent probe studies, with broad applications in chemistry and biology.

Synonyms: Ethyl 6-bromo-3-coumarincarboxylate

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Product Details of Ethyl 6-Bromocoumarin-3-carboxylate

CAS No. :2199-90-8
Formula : C12H9BrO4
M.W : 297.10
SMILES Code : O=C(C(C1=O)=CC2=C(O1)C=CC(Br)=C2)OCC
Synonyms :
Ethyl 6-bromo-3-coumarincarboxylate
MDL No. :MFCD00124584
InChI Key :RXGDNKCWEKUYQA-UHFFFAOYSA-N
Pubchem ID :691747

Safety of Ethyl 6-Bromocoumarin-3-carboxylate

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P264-P270-P301+P312-P330

Application In Synthesis of Ethyl 6-Bromocoumarin-3-carboxylate

* 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 [ 2199-90-8 ]

[ 2199-90-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2199-90-8 ]
  • [ 51175-79-2 ]
  • ethyl 6-bromo-4-[1-(methoxycarbonyl)cyclobutyl]-2-oxochroman-3-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
68% With mercury dichloride; zinc; In N,N,N,N,N,N-hexamethylphosphoric triamide; benzene; for 4h;Reflux; A mixture of 3 g of fine zinc chips, a catalytic amount of mercurybichloride, 20 ml of anhydrous benzene, 1 ml of HMPT, 12 mmol (2.32 g) of compound I, and 10 mmol (2.97 g) ofcompound II was boiled for 4 h, cooled, poured from zinc excess, hydrolyzed with 5% acetic acid; the organic layer wasseparated; reaction products were twice extracted with ethyl acetate from the water layer. After the extract was dried withanhydrous sodium sulfate the solvents were removed, and compound III was recrystallized from ethanol.
 

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