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Structure of 387-46-2
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2,6-Dihydroxybenzaldehyde features two hydroxyl groups positioned ortho to the aldehyde functionality, creating a rigid, electron-rich aromatic scaffold. This configuration enhances its reactivity in condensation and coupling reactions, particularly in the synthesis of polyphenolic architectures and chelating ligands. The molecule exhibits enhanced solubility in polar solvents and stability under standard bench conditions, facilitating handling in synthetic workflows.
2,6-Dihydroxybenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted phenolic scaffolds and heterocyclic systems. Its ortho-dihydroxy functionality facilitates metal chelation and oxidation-sensitive transformations, while the aldehyde group supports reductive amination, condensation reactions, and derivatization under mild conditions. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it valuable for medicinal chemistry and materials synthesis workflows.
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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: