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5400-79-3

Ethyl 3-oxocyclopentanecarboxylate

Catalog#: AR003QXH  |   CAS#: 5400-79-3  |   MDL#: MFCD01320352  |   MF: C8H12O3  |   MW: 156.1791

Packsize Purity Price Availability Quantity
100mg 98% $2.00 Global Stock Buy Now Add To Cart
250mg 98% $5.00 Global Stock Buy Now Add To Cart
1g 98% $10.00 Global Stock Buy Now Add To Cart
5g 98% $30.00 Global Stock Buy Now Add To Cart
10g 98% $48.00 Global Stock Buy Now Add To Cart
25g 98% $111.00 Global Stock Buy Now Add To Cart
100g 98% $354.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003QXH
Chemical Name Ethyl 3-oxocyclopentanecarboxylate
CAS Number 5400-79-3
Molecular Formula C8H12O3
Molecular Weight 156.1791
MDL Number MFCD01320352
SMILES CCOC(=O)C1CCC(=O)C1
NSC Number 10387

Ethyl 3-oxocyclopentanecarboxylate, also known as ethyl 3-oxocyclopentane-1-carboxylate, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in organic chemistry due to its ability to undergo various reactions and transformations, making it an essential component in the synthesis of numerous pharmaceuticals, agrochemicals, and fine chemicals.One of the primary applications of ethyl 3-oxocyclopentanecarboxylate is in the preparation of heterocyclic compounds. Its unique structure containing both a cyclic ketone and an ester group allows for the formation of diverse ring systems through cyclization reactions. This makes it a valuable intermediate in the synthesis of pyrrolidines, piperidines, and other important heterocycles found in many bioactive compounds.Furthermore, ethyl 3-oxocyclopentanecarboxylate can be utilized in the construction of chiral molecules. By incorporating this compound into asymmetric synthesis strategies, chemists can access enantiomerically pure substances with high optical purity, crucial in the development of pharmaceuticals and materials with specific stereochemical properties.In addition, the reactivity of ethyl 3-oxocyclopentanecarboxylate enables its involvement in various carbon-carbon and carbon-heteroatom bond-forming reactions. It can undergo transformations such as nucleophilic additions, condensations, and reductions to introduce new functional groups and structural motifs into a molecule, allowing for the creation of complex organic scaffolds with precise control over stereochemistry and regiochemistry.Overall, ethyl 3-oxocyclopentanecarboxylate's versatility and reactivity make it a valuable component in the toolbox of synthetic chemists, offering opportunities for the efficient and strategic construction of diverse organic compounds with tailored properties and functionalities.
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ACETIC ACID 4-OXO-CYCLOHEXYL ESTER

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methyl 3-oxocyclopentane-1-carboxylate

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tert-butyl 3-formyl-2,2-dimethylcyclopropane-1-carboxylate

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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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