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Structure of 7556-55-0
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4-Methyl-1-piperazinecarboxaldehyde features a reactive aldehyde group appended to a nitrogen-rich piperazine ring, enabling efficient conjugation in bioconjugation and medicinal chemistry applications. The methyl substituent enhances solubility and metabolic stability while preserving reactivity. This compound serves as a key scaffold for targeted drug discovery and functionalized probe development under standard conditions.
4-Methyl-1-piperazinecarboxaldehyde serves as a versatile building block in medicinal chemistry, enabling rapid access to diverse heterocyclic scaffolds through reductive amination, condensation, and cyclization reactions. Its aldehyde functionality exhibits high reactivity with amines and hydrazides under mild conditions, facilitating the construction of imines and hydrazones. The piperazine core provides enhanced solubility and metabolic stability, while the methyl group offers a handle for further functionalization. Bench-stable and readily purified by distillation or chromatography, it functions effectively in multi-step syntheses of bioactive molecules.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: