tert-Butyl 2-(5-amino-1H-pyrazol-3-yl)piperidine-1-carboxylate

95%

Reagent Code: #151210
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CAS Number 1396986-72-3

science Other reagents with same CAS 1396986-72-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.34 g/mol
Formula C₁₃H₂₂N₄O₂
badge Registry Numbers
MDL Number MFCD06656721
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drug molecules targeting inflammatory diseases, cancer, and central nervous system disorders. The protected amine group allows for selective reactions in multi-step syntheses, making it valuable in medicinal chemistry for building complex molecules with high specificity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,400.00
inventory 250mg
10-20 days ฿26,790.00

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tert-Butyl 2-(5-amino-1H-pyrazol-3-yl)piperidine-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drug molecules targeting inflammatory diseases, cancer, and central nervous system disorders. The protected amine group allows for selective reactions in multi-step syntheses, making it valuable in medicinal chemistry for building complex molecules with high specif

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drug molecules targeting inflammatory diseases, cancer, and central nervous system disorders. The protected amine group allows for selective reactions in multi-step syntheses, making it valuable in medicinal chemistry for building complex molecules with high specificity.

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