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Structure of 50270-27-4
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2,4,6-Trichloropyrimidine-5-carbaldehyde features a highly electrophilic aldehyde group flanked by three chlorine atoms on the pyrimidine ring, enabling selective conjugation in heterocyclic synthesis. This electron-deficient scaffold integrates readily into bioactive molecule frameworks, particularly in medicinal chemistry and agrochemical development.
2,4,6-Trichloropyrimidine-5-carbaldehyde serves as a versatile building block in medicinal and synthetic chemistry, enabling efficient construction of heterocyclic scaffolds. Its aldehyde functionality reacts readily with amines and nucleophiles under mild conditions, while the trichloropyrimidine core offers high reactivity for substitution reactions. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in API development and library generation.
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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: