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Structure of 52428-09-8
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4,7-Dimethoxy-2,3-dihydro-1H-inden-1-one features a fused bicyclic core with strategically positioned methoxy groups that enhance solubility and modulate electronic properties. This bench-stable ketone integrates readily into synthetic sequences requiring electron-donating substituents, offering predictable reactivity in transition metal-catalyzed transformations and serving as a key intermediate in the construction of complex heterocycles.
4,7-Dimethoxy-2,3-dihydro-1H-inden-1-one serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted indane scaffolds through standard functional group manipulations. Its ortho-dimethoxy substitution pattern enhances stability and facilitates electrophilic aromatic substitution or transition-metal-catalyzed coupling reactions. The molecule exhibits excellent bench stability, ease of purification, and compatibility with common protecting group strategies, making it well-suited for iterative synthetic sequences in API 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 : 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: