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Structure of 63124-55-0
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This bench-stable aldehyde features a rigid, electron-rich dioxole ring fused to a benzene core, enabling efficient coupling reactions. The para-carbaldehyde group provides a reactive handle for diverse synthetic transformations, while the 2,2-dimethyl substitution enhances steric protection and solubility in organic media.
2,2-Dimethylbenzo[d][1,3]dioxole-5-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive heterocyclic scaffolds. Its aldehyde functionality facilitates reductive amination, Wittig reactions, and coupling with nucleophiles under mild conditions. The dimethyl-substituted benzene ring enhances metabolic stability and provides steric shielding, improving bench stability and simplifying purification. This compound functions effectively in the synthesis of complex pharmaceutical intermediates and natural product analogs.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: