methyl-malonic ester

См. также в других словарях:

• Ester — For other uses, see Ester (disambiguation). A carboxylic acid ester. R and R denote any alkyl or aryl group, respectively Esters are chemical compounds derived by reacting an oxoacid with a hydroxyl compound such as an alcohol or phenol …   Wikipedia

• Acetoacetic ester synthesis — is a chemical reaction where ethyl acetoacetate is alkylated at the α carbon to both carbonyl groups and then converted into a ketone, or more specifically an α substituted acetone. This is very similar to malonic ester synthesis.:MechanismA… …   Wikipedia

• carboxylic acid — Chem. any organic acid containing one or more carboxyl groups. [1900 05; CARBOXYL + IC] * * * Any organic compound with the general chemical formula ―COOH in which a carbon (C) atom is bonded to an oxygen (O) atom by a double bond to make a… …   Universalium

• Methohexital — Systematic (IUPAC) name 5 hex 3 yn 2 yl 1 methyl 5 prop 2 enyl 1, 3 diazinane 2,4,6 trione Clinical data AHFS/Drugs.com …   Wikipedia

• Dimethyl malonate — Dimethyl malonate[1] IUPAC name propanedio …   Wikipedia

• Aldol reaction — The aldol reaction is a powerful means of forming carbon–carbon bonds in organic chemistry.[1][2][3] Discovered independently by …   Wikipedia

• Sodium thiopental — Systematic (IUPAC) name …   Wikipedia

• Ethyl acetoacetate — Chembox new Name = Ethyl acetoacetate ImageFile = Ethyl acetoacetate.png ImageName = Ethyl acetoacetate ImageFile1 = Ethyl acetoacetate 3d.png IUPACName = Ethyl 3 oxobutanoate OtherNames = Acetoacetic acid ethyl ester Ethyl acetylacetate 3… …   Wikipedia

• Dicarboxylic acid — Dicarboxylic acids are organic compounds that contain two carboxylic acid functional groups. In molecular formulae for dicarboxylic acids, these groups are often written as HOOC R COOH, where R may be an alkyl, alkenyl, alkynyl, or aryl group.… …   Wikipedia

• Phenobarbital — Systematic (IUPAC) name 5 ethyl 5 phenylpyrimidine …   Wikipedia

• Michael reaction — The Michael reaction or Michael addition is the nucleophilic addition of a carbanion or another nucleophile[1][2][3] to an alpha, beta unsaturated carbonyl compound. It belongs to the larger class of conjugate additions. This is one of the most… …   Wikipedia