1-Boc-4-(Benzo[d]isothiazol-3-yl-methyl-amino)-piperidine

≥95%

Reagent Code: #149725
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CAS Number 1002355-67-0

science Other reagents with same CAS 1002355-67-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 347.48 g/mol
Formula C₁₈H₂₅N₃O₂S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of central nervous system agents. Its structure allows for selective modification, making it valuable in creating compounds with potential antipsychotic or cognitive-enhancing properties. The Boc-protected amine group enables controlled deprotection and coupling in multi-step syntheses, especially in medicinal chemistry workflows targeting neurological disorders. Also employed in the preparation of receptor ligands where the piperidine and isothiazole moieties contribute to binding affinity and metabolic stability.

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inventory 1g
10-20 days ฿41,190.00

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1-Boc-4-(Benzo[d]isothiazol-3-yl-methyl-amino)-piperidine
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of central nervous system agents. Its structure allows for selective modification, making it valuable in creating compounds with potential antipsychotic or cognitive-enhancing properties. The Boc-protected amine group enables controlled deprotection and coupling in multi-step syntheses, especially in medicinal chemistry workflows targeting neurological disorders. Also employed in

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive molecules, particularly in the development of central nervous system agents. Its structure allows for selective modification, making it valuable in creating compounds with potential antipsychotic or cognitive-enhancing properties. The Boc-protected amine group enables controlled deprotection and coupling in multi-step syntheses, especially in medicinal chemistry workflows targeting neurological disorders. Also employed in the preparation of receptor ligands where the piperidine and isothiazole moieties contribute to binding affinity and metabolic stability.

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