tert-Butyl (1-(5-nitro-1H-benzo[d]imidazol-2-yl)piperidin-4-yl)carbamate

95%

Reagent Code: #141040
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CAS Number 1417794-13-8

science Other reagents with same CAS 1417794-13-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 361.4 g/mol
Formula C₁₇H₂₃N₅O₄
badge Registry Numbers
MDL Number MFCD22631650
inventory_2 Storage & Handling
Density 1.33±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical research as an intermediate in the synthesis of biologically active compounds, particularly in the development of antiparasitic and antimicrobial agents. The nitrobenzimidazole moiety is known for its role in enhancing activity against protozoal infections, while the carbamate-protected piperidine allows for selective modification in multi-step drug synthesis. Commonly employed in medicinal chemistry for optimizing lead compounds targeting infectious diseases.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,140.00
inventory 100mg
10-20 days ฿12,120.00

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tert-Butyl (1-(5-nitro-1H-benzo[d]imidazol-2-yl)piperidin-4-yl)carbamate
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Used in pharmaceutical research as an intermediate in the synthesis of biologically active compounds, particularly in the development of antiparasitic and antimicrobial agents. The nitrobenzimidazole moiety is known for its role in enhancing activity against protozoal infections, while the carbamate-protected piperidine allows for selective modification in multi-step drug synthesis. Commonly employed in medicinal chemistry for optimizing lead compounds targeting infectious diseases.

Used in pharmaceutical research as an intermediate in the synthesis of biologically active compounds, particularly in the development of antiparasitic and antimicrobial agents. The nitrobenzimidazole moiety is known for its role in enhancing activity against protozoal infections, while the carbamate-protected piperidine allows for selective modification in multi-step drug synthesis. Commonly employed in medicinal chemistry for optimizing lead compounds targeting infectious diseases.

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