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Structure of 1092352-55-0
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tert-Butyl 2-chloro-5H,6H,7H,8H-pyrido[4,3-d]pyrimidine-6-carboxylate features a sterically hindered tert-butyl ester and a chlorine-substituted pyridopyrimidine core. This bench-stable scaffold integrates readily into heterocyclic synthesis, serving as a key intermediate for pharmaceutical development.
tert-Butyl 2-chloro-5H,6H,7H,8H-pyrido[4,3-d]pyrimidine-6-carboxylate serves as a versatile building block for the synthesis of pyrido[4,3-d]pyrimidine-based scaffolds. The chloro group enables nucleophilic substitution reactions, facilitating access to diverse functionalized derivatives. Its tert-butyl ester moiety offers excellent bench stability and simplifies purification. This compound functions effectively in standard coupling protocols and is well-suited for medicinal chemistry campaigns targeting kinase inhibitors and other bioactive heterocycles.
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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-H320-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: