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Structure of 501907-61-5
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tert-Butyl (2,6-dichloropyridin-4-yl)carbamate features a pyridine core functionalized with chlorine atoms at the 2 and 6 positions, providing enhanced stability and electronic modulation. The tert-butyloxycarbonyl group enables efficient protection of amine intermediates during synthetic sequences. This derivative serves as a key building block in medicinal chemistry, particularly for constructing nitrogen-containing heterocycles under standard bench conditions.
tert-Butyl (2,6-dichloropyridin-4-yl)carbamate serves as a stable, bench-ready pyridine-based building block for medicinal chemistry and process development. The orthogonal protection of the amine enables selective deprotection under mild acidic conditions, facilitating downstream functionalization. Its 2,6-dichloro substitution pattern provides enhanced electrophilicity at C4, enabling efficient cross-coupling reactions with boronic acids and other nucleophiles. The tert-butyl carbamate group ensures high solubility and ease of purification, making it ideal for multi-step synthesis workflows requiring robust protection strategies.
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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: