CAS 13395-36-3
:Ethyl trimethylacetopyruvate
Description:
Ethyl trimethylacetopyruvate, with the CAS number 13395-36-3, is an organic compound that belongs to the class of pyruvate esters. It is characterized by its ester functional group, which is formed from the reaction of trimethylacetopyruvic acid and ethanol. This compound typically appears as a colorless to pale yellow liquid and is known for its fruity odor. Ethyl trimethylacetopyruvate is soluble in organic solvents, making it useful in various chemical applications, including as an intermediate in organic synthesis and in the production of pharmaceuticals. Its structure features a branched alkyl chain, which contributes to its unique chemical properties and reactivity. The compound may also exhibit biological activity, making it of interest in medicinal chemistry. However, as with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if ingested or inhaled. Overall, ethyl trimethylacetopyruvate is a versatile compound with potential applications in both industrial and research settings.
Formula:C10H16O4
InChI:InChI=1/C10H16O4/c1-5-14-9(13)7(11)6-8(12)10(2,3)4/h6,11H,5H2,1-4H3/b7-6-
InChI key:InChIKey=NIMKIMUBJFWPTD-UHFFFAOYSA-N
SMILES:C(CC(C(C)(C)C)=O)(C(OCC)=O)=O
Synonyms:- 5,5-Dimethyl-2,4-dioxohexanoic acid ethyl ester
- Ethyl 2,4-dioxo-5,5-dimethylhexanoate
- Ethyl 5,5-Dimethyl-2,4-Dioxohexanoate
- Ethyl 5,5-dimethyl-2,4-dioxohexanoate~Trimethylacetopyruvic acid ethyl ester
- Ethyl pivaloylpyruvate
- Hexanoic acid, 5,5-dimethyl-2,4-dioxo-, ethyl ester
- Pivaloylpyruvic acid ethyl ester
- ethyl (2Z)-2-hydroxy-5,5-dimethyl-4-oxohex-2-enoate
- 5,5-Dimethyl-2,4-dioxo-hexanoic acid ethyl ester
- 1ETHYL TRIMETHYLACETOPYRUVATE
- 2,4-Dioxo-5,5-dimethylhexanoic acid ethyl ester
- AKOS MSC-0258
- (Z)-ethyl 2-hydroxy-5,5-diMethyl-4-oxohex-2-enoate
- Ethyl trimethylacetopyruvate,98%
- Ethyl trimethyacetopyruvate, 98+%
- ETHYL TRIMETHYLACETOPYRUVATE
- Ethyl 5, 5-dimethyl2, 4-dioxo-1-hexanoate
- 3-Pivaloylpyruvic acid ethyl ester
- Ethyl (trimethylacetyl)pyruvate, Ethyl 5,5-dimethyl-2,4-dioxocaproate
- Ethyl-5,5-dimethyl-2,4-dioxohexanoat
- trimethylacetopyruvic acid ethyl ester
- See more synonyms
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Found 6 products.
Ethyl Trimethylacetopyruvate
CAS:Formula:C10H16O4Purity:>98.0%(GC)Color and Shape:Light yellow to Brown clear liquidMolecular weight:200.23Ethyl trimethylacetopyruvate, 98%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C10H16O4Purity:98%Color and Shape:Liquid, Clear colorless to pale yellowMolecular weight:200.23Ethyl 5,5-Dimethyl-2,4-dioxohexanoate
CAS:Formula:C10H16O4Purity:97%Color and Shape:LiquidMolecular weight:200.2316Ethyl 5,5-dimethyl-2,4-dioxohexanoate
CAS:<p>Ethyl 5,5-dimethyl-2,4-dioxohexanoate</p>Purity:97%Color and Shape:LiquidMolecular weight:200.23163g/molEthyl 5,5-Dimethyl-2,4-dioxohexanoate
CAS:Formula:C10H16O4Purity:97%Color and Shape:Liquid, OilMolecular weight:200.234Ethyl Trimethylacetopyruvate
CAS:<p>Ethyl Trimethylacetopyruvate is a chemical compound that belongs to the class of organic ester compounds. It has been shown to have high proton chemical stability and strong hydrogen bonding properties. This compound also has a chelate ring, which is formed through a reaction between an acid and a metal ion, such as ethyl acetate (CH3CO2CH3) or ethyl propionate (CH3CO2CH2CH3). Ethyl Trimethylacetopyruvate is synthesized by reacting ethanol with trimethylacetaldehyde in the presence of sulfuric acid. This process produces two products: Ethyl 2-methylpropanoate (Et2MP) and Ethyl 3-methylbutanoate (Et3MB). The molecule's x-ray diffraction data has been obtained using synchrotron radiation, which can be used to study the molecular structure and identify its purity.</p>Formula:C10H16O4Purity:Min. 95%Molecular weight:200.23 g/mol





