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Structure of 944109-65-3
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4-Chloro-5-methoxy-1-indanone is a sterically constrained, electron-deficient indanone derivative featuring a chloro group at the 4-position and a methoxy substituent at the 5-position. This configuration enhances electrophilicity at the carbonyl center, enabling efficient nucleophilic addition reactions. The compound exhibits excellent bench stability and solubility in common organic solvents, facilitating its use in synthetic transformations and medicinal chemistry applications.
4-Chloro-5-methoxy-1-indanone serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted indanone scaffolds through nucleophilic addition and subsequent functionalization. Its stability under standard reaction conditions, combined with orthogonal reactivity of the chloro and methoxy groups, facilitates selective transformations. The compound functions effectively in coupling reactions and heterocycle formation, offering predictable regiochemistry for downstream synthetic applications.
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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: