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Structure of 332370-72-6
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tert-Butyl N-(4-fluoro-3-nitrophenyl)carbamate delivers a moisture-tolerant, bench-stable platform for constructing fluorinated nitroarenes. The carbamate group enables straightforward deprotection under mild acidic conditions, while the para-fluoro and meta-nitro substituents provide orthogonal reactivity for downstream functionalization in medicinal chemistry and agrochemical synthesis.
tert-Butyl N-(4-fluoro-3-nitrophenyl)carbamate serves as a versatile building block in medicinal chemistry, enabling the introduction of both fluorinated and nitro functionalities in a single scaffold. The carbamate group provides stability during synthesis and can be selectively cleaved under mild acidic conditions. Its compatibility with standard cross-coupling reactions and tolerance to diverse functional groups make it well-suited for constructing complex heterocyclic intermediates and API precursors.
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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: