2-Oxo-2H-pyran-5-carboxylic acid methyl ester

CAS : 6018-41-3

Ref. 3D-FO57256

Informations sur le produit

• Nom: 2-Oxo-2H-pyran-5-carboxylic acid methyl ester
• Synonymes: Methyl coumalateMethyl 6-oxopyran-3-carboxylate, 2H-Pyran-5-carboxylic acid, 2-oxo-, methyl ester, 2H-Pyran-5-carboxylic acid, 2-oxo-, methyl ester (8CI)(9CI), 5-(Carbomethoxy)-2-pyrone, 5-(Methoxycarbonyl)-2-pyrone, Coumalic acid, methyl ester, Cumalic acid methyl ester, Glutaconic acid, 4-(hydroxymethylene)-, δ-lactone, methyl ester, Methyl 2-oxo-2H-pyran-5-carboxylate, Methyl 2-pyrone-5-carboxylate, Methyl cumalate, Nsc 137387, Nsc 34627

Description

2-Oxo-2H-pyran-5-carboxylic acid methyl ester is an activated form of 2-oxopyran. It reacts with nucleophiles, such as malic acid, to form ethyl esters. This reaction is an example of the Friedel-Crafts reaction, which is a type of electrophilic aromatic substitution. The rate of this reaction depends on the activation energies and fluorescence properties of the reactants. The mechanism for this reaction is that the double bond in the carbonyl group is ruptured by attacking nucleophiles, resulting in a release of hydrogen gas and formation of carboxylic acid derivatives. The product can be isolated using a solvent extraction technique or purified using column chromatography.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 154.12 g/mol
• Formule: C₇H₆O₄
• Degré de pureté: Min. 98 Area-%
• Couleur/Forme: Powder
• InChI: InChI=1S/C7H6O4/c1-10-7(9)5-2-3-6(8)11-4-5/h2-4H,1H3
• Code InChI: InChIKey=HHWWWZQYHPFCBY-UHFFFAOYSA-N
• SMILES: COC(=O)c1ccc(=O)oc1