CAS 30414-57-4
:6-Heptenoic acid, 3-oxo-, methyl ester
Description:
6-Heptenoic acid, 3-oxo-, methyl ester, with the CAS number 30414-57-4, is an organic compound characterized by its ester functional group and a double bond in its carbon chain. This compound features a seven-carbon backbone with a double bond located at the sixth carbon, and a ketone functional group at the third carbon, contributing to its reactivity and potential applications in organic synthesis. As a methyl ester, it is formed by the reaction of 6-heptenoic acid with methanol, resulting in a compound that is typically liquid at room temperature. The presence of both the double bond and the carbonyl group makes it a versatile intermediate in various chemical reactions, including those in the synthesis of pharmaceuticals and agrochemicals. Its properties, such as solubility and boiling point, are influenced by the molecular structure, and it may exhibit specific reactivity patterns typical of unsaturated carboxylic acid derivatives. Safety data should be consulted for handling, as with all chemical substances.
Formula:C8H12O3
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Found 2 products.
Methyl 3-oxohept-6-enoate
CAS:<p>Methyl 3-oxohept-6-enoate is a cyclopropane, which is a type of organic compound that contains one or more rings of carbon atoms. This compound can be synthesized by the chemoenzymatic process using hydrogen chloride and activated methylene chloride. The synthesis starts with an acidic condensation process, followed by the hydroalkylation of methyl 3-oxoheptanoate. The resulting product is then isolated through a chiral synthetic process and has an isolated yield of 51%.</p>Formula:C8H12O3Purity:Min. 95%Molecular weight:156.18 g/mol
