Ethyl 2-methylacetoacetate

CAS: 609-14-3

Ref. 3D-FE22977

Información del producto

• Nombre: Ethyl 2-methylacetoacetate
• Sinónimos: 2-Methyl-3-oxo-butanoic acid ethyl esterα-Methyl-acetoacetic acid ethyl ester2-Methyl-3-oxobutanoic acid ethyl ester, 2-Methyl-3-oxobutanoic acid ethyl ester, 2-Methyl-3-oxobutyric acid ethyl ester, 2-Methylacetessigsaeure-Aethylester, 2-Methylacetoacetate d'ethyle, 2-Methylacetoacetic acid ethyl ester, 2-Metilacetoacetato De Etilo, Acetoacetic acid, 2-methyl-, ethyl ester, Acetoacetic acid, α-methyl-, ethyl ester, Alpha-(Aminomethyl)-4-Hydroxy-1,3-Benzenedimethanol, Butanoic acid, 2-methyl-3-oxo-, ethyl ester, Ethyl 2-Methyl-3-Oxobutanoate, Ethyl 2-acetylpropanoate, Ethyl 2-acetylpropionate, Ethyl 2-methyl-3-oxobutyrate, Ethyl 2-methylacetacetate, Ethyl 3-oxo-2-methylbutanoate, Ethyl methylacetoacetate, Ethyl α-acetylpropionate, Ethyl α-methylacetoacetate, Ethyl α-methylacetylacetate, Ethyl-2-methylacetoacetat, Nsc 1102, ethyl (2R)-2-methyl-3-oxobutanoate, ethyl (2S)-2-methyl-3-oxobutanoate, α-Methyl acetoacetic acetate, α-Methylacetoacetic ester

Descripción

Ethyl 2-methylacetoacetate is an organic compound with the formula CH3COOC2H5. It is a colorless liquid that is soluble in water and alcohols. Ethyl 2-methylacetoacetate has been shown to have antiinflammatory activity and can be used to treat HIV infections. The transport rate of ethyl 2-methylacetoacetate has been shown to be higher than other esters, such as ethyl acetoacetate. Acetylation reactions are typically catalyzed by acid or base, but the reaction mechanism of this compound has not yet been elucidated. X-ray crystal structures show that ethyl 2-methylacetoacetate reacts with basic proteins such as sodium carbonate, leading to cell lysis.

• Marca: Biosynth

Propiedades químicas

• Peso molecular: 144.17 g/mol
• Fórmula: C₇H₁₂O₃
• Pureza: Min. 98 Area-%
• Color/Forma: Colorless Clear Liquid
• InChI: InChI=1S/C7H12O3/c1-4-10-7(9)5(2)6(3)8/h5H,4H2,1-3H3
• Clave InChI: InChIKey=FNENWZWNOPCZGK-UHFFFAOYSA-N
• SMILES: CCOC(=O)C(C)C(C)=O