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Structure of 60899-34-5
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This electron-deficient indenone derivative features a conjugated carbonitrile group, enabling direct integration into heterocyclic synthesis. The planar, aromatic core facilitates efficient coupling reactions under mild conditions. Bench-stable and moisture-tolerant, it serves as a robust scaffold for constructing functionalized polycycles in medicinal chemistry and materials science.
2,3-Dihydro-1-oxo-1H-indene-4-carbonitrile serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted indenone derivatives and heterocyclic scaffolds. Its conjugated enone–nitrile functionality supports diverse transformations including nucleophilic additions, Michael reactions, and transition-metal-catalyzed couplings. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis campaigns in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: