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Structure of 90111-15-2
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3,2-Cresotaldehyde features a strategically positioned aldehyde group flanked by methyl substituents at the 3- and 2-positions of the aromatic ring. This electron-rich scaffold enables direct integration into coupling reactions and serves as a key building block for heterocyclic systems in synthetic medicinal chemistry.
3,2-Cresotaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of substituted heterocycles and functionalized alkenes. Its ortho-substituted aldehyde functionality exhibits enhanced stability and predictable reactivity in nucleophilic additions and condensation reactions. The molecule functions effectively in standard coupling protocols and offers excellent purification characteristics due to its defined polarity and low volatility, making it well-suited for bench-scale synthesis and process 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: