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Structure of 310400-38-5
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5,6-Dichloro-4-pyrimidinamine features a pyrimidine core bearing two chlorine substituents at the 5 and 6 positions and an amino group at the 4 position. This electron-deficient heterocycle serves as a key scaffold for medicinal chemistry applications, enabling direct incorporation into kinase inhibitors and antiviral agents. The compound exhibits bench-stable handling characteristics and compatibility with standard coupling reactions under mild conditions.
5,6-Dichloro-4-pyrimidinamine serves as a versatile building block for the synthesis of pyrimidine-based scaffolds in medicinal chemistry and agrochemical research. Its dual chloro substituents enable efficient nucleophilic substitution reactions, facilitating the introduction of diverse aryl, heteroaryl, and amino groups under mild conditions. The compound exhibits good bench stability and is readily purified by standard chromatographic methods, making it well-suited for use in multi-step synthetic sequences requiring functional group tolerance and predictable reactivity.
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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: