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Structure of 120977-94-8
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2,6-Dichloro-3H-pyrimidin-4-one is a bench-stable, electron-deficient heterocycle featuring two chlorine substituents at the 2 and 6 positions. This configuration enhances its reactivity in nucleophilic substitution processes, enabling efficient coupling with amines and other nucleophiles under mild conditions. The compound serves as a key building block for bioactive pyrimidine derivatives in medicinal chemistry and materials science applications.
2,6-Dichloro-3H-pyrimidin-4-one serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyrimidine scaffolds. Its electrophilic C2 and C6 positions facilitate nucleophilic substitution under mild conditions, supporting the construction of diverse heterocyclic systems. The compound exhibits excellent bench stability and compatibility with common functional groups, simplifying purification and integration into multi-step syntheses.
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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: