CAS 26501-83-7
:3-Furancarboxylicacid, 5-methyl-, ethyl ester
Description:
3-Furancarboxylic acid, 5-methyl-, ethyl ester, commonly referred to as ethyl 5-methyl-3-furancarboxylate, is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing oxygen. This compound features a carboxylic acid functional group that has been esterified with ethanol, resulting in its ethyl ester form. It typically appears as a colorless to pale yellow liquid with a pleasant, fruity odor. The presence of the methyl group at the 5-position of the furan ring influences its reactivity and solubility properties, making it more lipophilic. This compound is often used in organic synthesis and may serve as a building block in the production of various pharmaceuticals, agrochemicals, and flavoring agents. Its chemical stability and relatively low toxicity make it suitable for various applications in the chemical industry. As with many esters, it can undergo hydrolysis in the presence of water, reverting to the corresponding acid and alcohol.
Formula:C8H10O3
Synonyms:- 3-Furoicacid, 5-methyl-, ethyl ester (8CI)
- Ethyl 2-methyl-4-furoate
- Ethyl5-methylfuran-3-carboxylate
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Found 4 products.
3-Furancarboxylic acid, 5-methyl-, ethyl ester
CAS:Formula:C8H10O3Purity:98%Molecular weight:154.1632Ethyl 5-methylfuran-3-carboxylate
CAS:Ethyl 5-methylfuran-3-carboxylatePurity:98%Molecular weight:154.16g/molEthyl 5-methylfuran-3-carboxylate
CAS:<p>Ethyl 5-methylfuran-3-carboxylate is a synthetic, unsaturated, unsaturated lactone. It is used as a precursor to the synthesis of dienes, esters and other compounds. In one example, ethyl 5-methylfuran-3-carboxylate was converted to ethyl 2-(5-methylthiophenoxy)propionate in a three step sequence that involved the use of anhydrous pyridine and an acid catalyst. The resulting product was used in the synthesis of a variety of organic compounds including an antiarrhythmic drug.</p>Formula:C8H10O3Purity:Min. 95%Molecular weight:154.16 g/mol



