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Structure of 22065-85-6
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1-Benzylpiperidine-4-carbaldehyde features a conjugated aldehyde group positioned at the para position relative to the piperidine nitrogen, enabling efficient coupling in reductive amination workflows. The benzyl substituent enhances solubility and electronic modulation, while the aldehyde moiety offers high reactivity for building complex heterocycles and bioactive molecules under standard conditions.
1-Benzylpiperidine-4-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to diverse heterocyclic scaffolds. Its aldehyde functionality facilitates standard transformations including reductive amination, Wittig reactions, and cyanohydrin formation. The benzylpiperidine core offers favorable metabolic stability and lipophilicity profiles, making it valuable for optimizing pharmacokinetic properties in CNS-targeted compounds. Bench-stable and readily purified by chromatography, it functions effectively in multi-step syntheses requiring functional group compatibility.
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GHS Pictogram :
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GHS No : GHS05,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-H318
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Precautionary Statements : P264-P270-P280-P330-P405-P501
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Lot numbers can be found on the outside label of a product: