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Structure of 30084-91-4
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This bench-stable aldehyde features a fused bicyclic structure with a reactive carbonyl at the 5-position, enabling direct incorporation into synthesis workflows. The electron-rich indene core enhances reactivity in nucleophilic addition and coupling reactions, while the dihydro substitution maintains compatibility with standard organic protocols.
2,3-Dihydro-1H-indene-5-carbaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted indene scaffolds. Its aldehyde functionality facilitates standard transformations including reductive amination, Grignard additions, and Wittig reactions, while the fused bicyclic framework offers rigidity and defined stereochemistry. Bench-stable and amenable to purification via chromatography or crystallization, it functions reliably in multi-step syntheses targeting pharmaceutical intermediates and functional materials.
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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: