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Structure of 131056-76-3
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tert-Butyl 2-oxotetrahydropyrimidine-1(2H)-carboxylate serves as a key scaffold in heterocyclic synthesis, featuring a bench-stable carbamate group and a reactive ketone moiety. This compound integrates readily into medicinal chemistry campaigns, enabling efficient access to pyrimidine-based pharmacophores through selective functionalization at the carbonyl site.
tert-Butyl 2-oxotetrahydropyrimidine-1(2H)-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds through reductive amination and subsequent functionalization. The ketone group facilitates selective transformations, while the tert-butyl ester provides stability and ease of removal under mild acidic conditions. Its compatibility with diverse reaction conditions makes it valuable for medicinal chemistry campaigns requiring rapid scaffold diversification.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: