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Structure of 956523-98-1
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tert-Butyl (6-formylpyridin-2-yl)carbamate features a pyridine scaffold with orthogonal functional handles: a formyl group at the 6-position and a carbamate-protected amine at the 2-position. This bifunctional architecture enables selective coupling in late-stage diversification, particularly in medicinal chemistry applications requiring precise spatial control. The tert-butyl carbamate serves as a stable, bench-stable amine equivalent that can be removed under mild acidic conditions.
tert-Butyl (6-formylpyridin-2-yl)carbamate serves as a versatile building block in medicinal chemistry, enabling direct access to functionalized pyridine scaffolds. The formyl group facilitates efficient transformations including reductive amination, Wittig reactions, and nucleophilic additions, while the carbamate protects the amine under standard reaction conditions. Its bench-stable nature and compatibility with diverse synthetic workflows make it ideal for constructing bioactive heterocycles and drug candidates.
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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: