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Structure of 1354223-67-8
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tert-Butyl (2-chloro-5-fluoropyridin-4-yl)carbamate serves as a key building block in medicinal chemistry, featuring a fluorinated pyridine core with orthogonal functional handles. The carbamate group enables stable protection of amines during synthesis, while the chloro and fluoro substituents provide tunable electronic and steric profiles for downstream coupling reactions. This derivative exhibits excellent bench stability and compatibility with diverse reaction conditions.
tert-Butyl (2-chloro-5-fluoropyridin-4-yl)carbamate serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the 4-position of fluorinated pyridines. The carbamate group provides excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. It participates reliably in palladium-catalyzed cross-coupling reactions, including Suzuki and Buchwald–Hartwig transformations, due to its compatibility with diverse reaction conditions and tolerance for common functional groups.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: