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Structure of 14160-91-9
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4,6-Dichloro-2-methylpyrimidine-5-carbaldehyde features a reactive aldehyde group flanked by electron-withdrawing chlorine atoms and a methyl substituent, enabling selective coupling in heterocyclic synthesis. This bench-stable scaffold integrates readily into pharmaceutical intermediates and functional materials, offering high compatibility with nucleophilic addition and condensation reactions under standard conditions.
4,6-Dichloro-2-methylpyrimidine-5-carbaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of pyrimidine-based scaffolds. Its dual electrophilic sites—chlorine atoms at C4 and C6—facilitate selective substitution, while the aldehyde group provides a handle for reductive amination, oxime formation, or coupling reactions. Bench-stable and compatible with standard reaction conditions, it functions effectively in medicinal chemistry campaigns requiring functionalized pyrimidines.
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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: