Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. 87-13-8, formula is C10H16O5, Name is Diethyl 2-(ethoxymethylene)malonate. They perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Electric Literature of 87-13-8.
Hassen, Manel Ben;Masmoudi, Fatma;Zribi, Lazhar;Trigui, Mohamed;Ismaili, Lhassane;Marco-Contelles, Jose;Chabchoub, Fakher research published 《 Regioselective Synthesis of Novel [1,2,4]Triazolo[1,5-a]pyridine Derivatives》, the research content is summarized as follows. Herein, the reaction of 2-(5-aryl-4H-1,2,4-triazol-3-yl)acetonitriles I (R = H, Me) with appropriate Michael acceptors (E)-R1C(OCH2CH3)=C(R2)R3 (R1 = H, Me, Et; R2 = CN, C(O)OCH2CH3; R3 = CN, C(O)OCH2CH3) gives novel [1,2,4]triazolo[1,5-a]pyridines II and III whose antioxidant properties have been investigated. A plausible reaction mechanism, supported by DFT calculations, has been proposed to explain the total observed regioselective formation of [1,2,4]triazolo[1,5-a]pyridine derivatives II and III depending on the type of substituents on the Michael acceptor.
87-13-8, Diethyl ethoxymethylenemalonate is a useful research compound. Its molecular formula is C10H16O5 and its molecular weight is 216.23 g/mol. The purity is usually 95%.
Diethyl ethoxymethylidenemalonate is a matrix effect reagent used in analytical chemistry. It is often used as a substrate for the cycloaddition process, which produces malondialdehyde and hydrochloric acid. The UV-absorption of the malondialdehyde can be measured to determine the concentration of the sample. Diethyl ethoxymethylidenemalonate is also used as a dna template in binding constants, where it binds with amines to form complexes that are then analyzed by light emission. It has been shown to have an inhibitory effect on gyrase and trifluoroacetic acid, both enzymes involved in DNA replication., Electric Literature of 87-13-8
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics