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Structure of 20010-99-5
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2-Aminomethylpyrazine delivers a bifunctional scaffold combining a pyrazine core with a reactive aminomethyl group, enabling straightforward conjugation in synthetic medicinal chemistry. This bench-stable heterocycle integrates readily into drug discovery libraries and serves as a key building block for targeted bioconjugates.
2-Aminomethylpyrazine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrazine-based pharmacophores. The primary amine functionality facilitates straightforward derivatization via amidation, alkylation, and reductive amination, while the pyrazine core offers enhanced metabolic stability and favorable physicochemical properties. Its bench-stable nature and compatibility with standard purification protocols make it well-suited for iterative synthesis workflows in API development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2810
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: