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Structure of 90905-33-2
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2-Methylpyrimidine-5-carbaldehyde features a pyrimidine core with strategically positioned methyl and aldehyde groups, enabling direct incorporation into heterocyclic scaffolds. This electron-deficient aldehyde serves as a reactive handle for nucleophilic additions, facilitating the synthesis of functionalized pharmaceutical intermediates under mild conditions.
2-Methylpyrimidine-5-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds through standard carbonyl transformations. Its aldehyde functionality facilitates reductive amination, Grignard additions, and condensation reactions with amines or hydrazines, while the electron-deficient pyrimidine ring enhances reactivity in nucleophilic substitution processes. Bench-stable and readily purified by column chromatography, it functions as a key intermediate in the synthesis of kinase inhibitors and other bioactive heterocycles.
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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: