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Structure of 220032-26-8
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This benzamide derivative features a piperidin-4-ylmethyl substituent that enhances solubility and modulates bioavailability. The para-amino and ortho-chloro groups establish electron-deficient character, while the methoxy moiety contributes to steric and electronic tuning. It serves as a key intermediate in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
4-Amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide serves as a versatile scaffold in medicinal chemistry, enabling the construction of diverse heterocyclic systems and bioactive molecules. The molecule combines a chlorinated aniline core with a methoxy group and a piperidinylmethyl amide, offering orthogonal functional handles for downstream derivatization. Its bench-stable nature and compatibility with standard coupling and cyclization protocols facilitate efficient synthesis of targeted compounds.
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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: