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Structure of 4214-73-7
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2-Amino-5-cyanopyridine features a dual functionalization pattern with an amino group and a cyano moiety positioned ortho to each other on the pyridine ring. This arrangement enables efficient integration into heterocyclic architectures, particularly in medicinal chemistry scaffolds and transition metal-catalyzed coupling reactions. The molecule exhibits enhanced solubility and stability under standard conditions, facilitating its use in synthetic workflows.
2-Amino-5-cyanopyridine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via nucleophilic addition and coupling reactions. Its dual functionality—amine and nitrile groups—facilitates orthogonal transformations, including amidation, cyclization, and transition-metal-catalyzed cross-couplings. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for scalable medicinal chemistry campaigns and API intermediate development.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302-H312-H314-H332
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P304+P341-P305+P351+P338-P310-P312-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: