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Structure of 23906-13-0
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2-Hydrazinyl-4,6-dimethylpyrimidine delivers a reactive hydrazino handle for conjugation and cyclization reactions. The electron-rich pyrimidine core enhances nucleophilicity, while methyl groups provide steric stabilization. This bench-stable reagent integrates efficiently into synthetic sequences requiring selective N–N bond formation under mild conditions.
2-Hydrazinyl-4,6-dimethylpyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds through condensation and cyclization reactions. Its hydrazinyl group exhibits reliable reactivity with carbonyl compounds and electrophiles, facilitating the construction of fused heterocycles and functionalized derivatives. The dimethyl substitution enhances bench stability and solubility, supporting straightforward isolation and purification. This compound functions effectively in standard synthetic workflows for medicinal chemistry and materials science applications.
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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: