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597-04-6

2,2-Dimethyl-3-oxo-butyric acid ethyl ester

Catalog#: AR00EAG7  |   CAS#: 597-04-6  |   MDL#: MFCD06658443  |   MF: C8H14O3  |   MW: 158.195

Packsize Purity Price Availability Quantity
50mg 95% $52.00 2-3 weeks Buy Now Add To Cart
100mg 95% $61.00 2-3 weeks Buy Now Add To Cart
250mg 95% $76.00 2-3 weeks Buy Now Add To Cart
500mg 95% $105.00 2-3 weeks Buy Now Add To Cart
1g 95% $129.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $244.00 2-3 weeks Buy Now Add To Cart
5g 95% $435.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00EAG7
Chemical Name 2,2-Dimethyl-3-oxo-butyric acid ethyl ester
CAS Number 597-04-6
Molecular Formula C8H14O3
Molecular Weight 158.195
MDL Number MFCD06658443
SMILES CCOC(=O)C(C(=O)C)(C)C
NSC Number 29039

Ethyl 2,2-dimethyl-3-oxobutanoate, also known as Diethyl acetylmalonate, is a versatile compound widely used in organic synthesis. This compound serves as a valuable building block in the preparation of various organic compounds due to its unique structural characteristics.In chemical synthesis, Ethyl 2,2-dimethyl-3-oxobutanoate is commonly employed as a key intermediate in the synthesis of complex molecules such as pharmaceuticals, agrochemicals, and specialty chemicals. Its enolizable nature makes it a suitable substrate for a variety of reactions, including alkylation, acylation, and condensation reactions.One prominent application of Ethyl 2,2-dimethyl-3-oxobutanoate is in the synthesis of pyrazoles, which are important heterocyclic compounds with diverse biological activities. By reacting Ethyl 2,2-dimethyl-3-oxobutanoate with hydrazine derivatives, pyrazole derivatives can be efficiently synthesized through cyclization reactions.Additionally, Ethyl 2,2-dimethyl-3-oxobutanoate can undergo Michael addition reactions with various nucleophiles, enabling the introduction of functional groups at the β-carbon position. This reactivity is particularly useful in the construction of carbon-carbon bonds and the creation of structural diversity in organic molecules.Overall, Ethyl 2,2-dimethyl-3-oxobutanoate plays a crucial role in chemical synthesis by serving as a key intermediate for the preparation of complex organic compounds with diverse applications in the fields of pharmaceuticals, agrochemicals, and materials science.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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