tert-Butyl 4-(1H-indazol-3-yl)piperidine-1-carboxylate

≥95%

Reagent Code: #148762
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CAS Number 889945-69-1

science Other reagents with same CAS 889945-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.38 g/mol
Formula C₁₇H₂₃N₃O₂
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Its structure supports the formation of biologically active molecules that target specific signaling pathways in tumor cells. Commonly employed in medicinal chemistry for constructing indazole-based scaffolds, which are known for their high binding affinity to enzyme active sites. Also utilized in research settings to design compounds with improved metabolic stability and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,850.00
inventory 250mg
10-20 days ฿6,920.00

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tert-Butyl 4-(1H-indazol-3-yl)piperidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Its structure supports the formation of biologically active molecules that target specific signaling pathways in tumor cells. Commonly employed in medicinal chemistry for constructing indazole-based scaffolds, which are known for their high binding affinity to enzyme active sites. Also utilized in research settings to design compounds with improved metabolic stabi

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Its structure supports the formation of biologically active molecules that target specific signaling pathways in tumor cells. Commonly employed in medicinal chemistry for constructing indazole-based scaffolds, which are known for their high binding affinity to enzyme active sites. Also utilized in research settings to design compounds with improved metabolic stability and selectivity.

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