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Structure of 52977-63-6
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4,7-Dichloro-2,3-dihydro-1H-inden-1-one is a chlorinated indenone derivative featuring two chlorine atoms at the 4 and 7 positions, conferring enhanced electron-withdrawing character. This sterically accessible scaffold serves as a key building block in synthetic routes to functionalized heterocycles and bioactive molecules. The compound exhibits bench-stable handling under standard conditions and integrates readily into transition metal-catalyzed coupling processes.
4,7-Dichloro-2,3-dihydro-1H-inden-1-one serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of substituted indene scaffolds. Its dichloro substitution pattern enhances electrophilic reactivity at the carbonyl-adjacent positions, facilitating nucleophilic additions and transition-metal-catalyzed couplings. The compound exhibits good bench stability and compatibility with standard purification methods, making it well-suited for use in medicinal chemistry campaigns and API intermediate synthesis.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: