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Structure of 19828-20-7
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2-Amino-5-acetylpyridine features a pyridine core functionalized with an amino group at the 2-position and an acetyl moiety at the 5-position, delivering a versatile scaffold for medicinal chemistry. The electron-donating amino group enhances reactivity at the ring, while the acetyl substituent provides a handle for derivatization. This compound exhibits favorable solubility and stability under standard bench conditions, enabling straightforward integration into synthetic sequences.
2-Amino-5-acetylpyridine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based pharmacophores. Its amino and acetyl groups offer orthogonal reactivity for Suzuki couplings, amidations, and electrophilic substitutions, facilitating the construction of complex heterocyclic scaffolds. The compound exhibits good bench stability and ease of purification, making it well-suited for high-throughput synthesis and process development workflows.
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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: