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Structure of 1062134-26-2
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tert-Butyl (5-amino-6-methylpyridin-2-yl)carbamate features a pyridine scaffold with a methyl group at C6 and a primary amine at C5, enabling direct functionalization in medicinal chemistry. The tert-butoxycarbonyl (Boc) protecting group ensures stability during synthesis and facilitates selective deprotection under mild acidic conditions. This compound serves as a key intermediate for nitrogen-containing heterocycles in drug discovery pipelines.
tert-Butyl (5-amino-6-methylpyridin-2-yl)carbamate serves as a versatile building block in medicinal chemistry, enabling direct access to functionalized pyridine scaffolds. The protected amine facilitates selective transformations, while the 6-methyl group provides steric and electronic modulation. Its bench-stable carbamate moiety allows for straightforward deprotection under mild acidic conditions, supporting efficient synthesis of target molecules in multi-step sequences.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: