Ethyl 3-oxobutanoate

CAS : 141-97-9

Ref. 3D-FE12158

Informations sur le produit

• Nom: Ethyl 3-oxobutanoate
• Synonymes: Ethyl acetoacetate, 1-Ethoxybutane-1,3-dione, 2-Ethyl-3-Oxobutanoate, 3-Oxobutanoic acid ethyl ester, 3-Oxobutyric acid ethyl ester, Acetessigsaeure-Aethylester, Acetoacetate d'ethyle, Acetoacetate, Ethyl, Acetoacetato De Etilo, Acetoacetic acid ethyl ester, Acetoacetic ester, Acetylacetic acid ethyl ester, Butanoic acid, 3-oxo-, ethyl ester, EAA, Ethyl 2-acetoacetate, Ethyl 2-methyl-3-oxopropionate, Ethyl 3-Oxobutanate, Ethyl 3-ketobutyrate, Ethyl 3-oxobutyrate, Ethyl acetonecarboxylate, Ethyl acetylacetate, Ethyl beta-ketobutyrate, Ethylacetoacetat, Labotest-Bb Lt01690211, Nsc 37390, Nsc 8657
• CAS: 141-97-9

Description

Ethyl 3-oxobutanoate (E3OB) is a sterically active compound with high values. It has been shown to inhibit the replication of HIV and other retroviruses. E3OB inhibits viral replication by binding to the enzyme reverse transcriptase, which is responsible for converting RNA into DNA. The reaction mechanism of E3OB is as follows: it reacts with the substrate film and forms an ester hydrochloride, which then reacts with malonic acid to form a coumarin derivative. This derivative interacts with wild-type HIV strain and inhibits its replication.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 130.14 g/mol
• Formule: C₆H₁₀O₃
• Degré de pureté: Min. 98%
• Couleur/Forme: Clear Liquid
• InChI: InChI=1S/C6H10O3/c1-3-9-6(8)4-5(2)7/h3-4H2,1-2H3
• Code InChI: InChIKey=XYIBRDXRRQCHLP-UHFFFAOYSA-N
• SMILES: CCOC(=O)CC(C)=O