tert-Butyl 4-(6-nitro-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate

97%

Reagent Code: #141769
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CAS Number 889942-01-2

science Other reagents with same CAS 889942-01-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 362.3804 g/mol
Formula C₁₇H₂₂N₄O₅
badge Registry Numbers
MDL Number MFCD07776419
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drugs targeting inflammatory, neurological, and oncological conditions. The nitro group allows for further functionalization, enabling derivatization for structure-activity relationship studies. Commonly employed in medicinal chemistry research for designing potent and selective small-molecule therapeutics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿28,800.00
inventory 250mg
10-20 days ฿48,000.00

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tert-Butyl 4-(6-nitro-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drugs targeting inflammatory, neurological, and oncological conditions. The nitro group allows for further functionalization, enabling derivatization for structure-activity relationship studies. Commonly employed in medicinal chemistry research for designing

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drugs targeting inflammatory, neurological, and oncological conditions. The nitro group allows for further functionalization, enabling derivatization for structure-activity relationship studies. Commonly employed in medicinal chemistry research for designing potent and selective small-molecule therapeutics.

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