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Structure of 148256-82-0
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4-Chloro-2-(methylsulfanyl)pyrimidine-5-carbaldehyde features a pyrimidine core bearing a chloro group, a methylthio substituent, and a formyl function at the 5-position. This electron-deficient scaffold integrates readily into heterocyclic syntheses, offering high reactivity in nucleophilic addition and coupling processes. The aldehyde functionality enables direct conjugation with amines or hydrazines under mild conditions. Bench-stable and moisture-tolerant, it serves as a key building block for pharmaceutical intermediates and functional materials.
4-Chloro-2-(methylsulfanyl)pyrimidine-5-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The aldehyde group facilitates nucleophilic additions and condensation reactions, while the chloro and methylthio substituents offer orthogonal reactivity for downstream functionalization. Bench-stable and compatible with standard purification methods, it functions effectively in coupling and heterocycle-forming processes common to API 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: