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Structure of 1197953-49-3
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This dimethylphosphine oxide features a 2,5-dichloropyrimidin-4-ylamino-substituted phenyl scaffold, delivering enhanced electronic tuning and steric bulk. The phosphine oxide moiety provides robust stability and facilitates coordination in transition metal catalysis. Its bench-stable nature enables straightforward handling in synthetic workflows.
(2-((2,5-Dichloropyrimidin-4-yl)amino)phenyl)dimethylphosphine oxide serves as a versatile building block in medicinal chemistry, enabling efficient construction of functionalized heterocycles via palladium-catalyzed cross-coupling. The dichloropyrimidine moiety provides high reactivity in nucleophilic substitution, while the dimethylphosphine oxide group offers excellent stability and compatibility with diverse reaction conditions. Its bench-stable nature and orthogonal reactivity facilitate streamlined synthesis of complex scaffolds relevant to kinase inhibitor development and other pharmaceutical applications.
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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: