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58610-66-5

Ethyl 6′-cyano-α-ethyl-2′,3′-dihydro-5′-oxospiro[1,3-dioxolane-2,1′(5′H)-indolizine]-7′-acetate

Catalog#: AR01X3TC  |   CAS#: 58610-66-5  |   MDL#: MFCD20133738  |   MF:  |   MW:

Packsize Purity Price Availability Quantity
100mg 97% $662.00 Global Stock Buy Now Add To Cart
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Catalog Number AR01X3TC
Chemical Name Ethyl 6′-cyano-α-ethyl-2′,3′-dihydro-5′-oxospiro[1,3-dioxolane-2,1′(5′H)-indolizine]-7′-acetate
CAS Number 58610-66-5
MDL Number MFCD20133738

Ethyl 2-(6-cyano-5-oxo-2,3-dihydro-5H-spiro[indolizine-1,2'-[1,3]dioxolan]-7-yl)butanoate is a versatile compound commonly used in chemical synthesis for its unique structural properties and reactivity. Its spirocyclic core containing an indolizine ring and a dioxolane moiety makes it a valuable building block in the synthesis of various heterocyclic compounds and pharmaceutical agents.In chemical synthesis, this compound can serve as a key intermediate for the construction of complex organic molecules through a series of transformations. It can undergo various functional group modifications and reactions, such as nucleophilic addition, cyclization, and substitution, to afford diverse molecular scaffolds. The cyano group can participate in a range of organic reactions, expanding the chemical versatility of the compound.Additionally, the ester functionality of Ethyl 2-(6-cyano-5-oxo-2,3-dihydro-5H-spiro[indolizine-1,2'-[1,3]dioxolan]-7-yl)butanoate provides opportunities for further derivatization and diversification of the molecule, allowing for the introduction of different functional groups or stereochemical motifs. This enables chemists to tailor the compound towards specific synthetic targets or biological activities.Overall, the strategic incorporation of Ethyl 2-(6-cyano-5-oxo-2,3-dihydro-5H-spiro[indolizine-1,2'-[1,3]dioxolan]-7-yl)butanoate in chemical synthesis offers a valuable platform for the efficient and versatile construction of complex molecules with potential applications in drug discovery, material science, and agrochemical development.
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