tert-Butyl ((2R,3S)-5-oxo-2-(2,4,5-trifluorophenyl)tetrahydro-2H-pyran-3-yl)carbamate

98%

Reagent Code: #123603
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CAS Number 951127-24-5

science Other reagents with same CAS 951127-24-5

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scatter_plot Molecular Information
Weight 345.31 g/mol
Formula C₁₆H₁₈F₃NO₄
badge Registry Numbers
MDL Number MFCD20926097
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of complex pharmaceutical agents, particularly in the development of protease inhibitors. Its structural features make it a valuable intermediate in the production of drugs targeting viral infections, including HIV and hepatitis C. The presence of the trifluorophenyl group enhances its binding affinity to specific enzyme targets, improving the efficacy of the final drug product. Additionally, the tert-butyl carbamate moiety provides stability during synthetic processes, ensuring the integrity of the compound in multi-step reactions. Its application is critical in medicinal chemistry for creating potent and selective therapeutic agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿49,500.00

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tert-Butyl ((2R,3S)-5-oxo-2-(2,4,5-trifluorophenyl)tetrahydro-2H-pyran-3-yl)carbamate
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This compound is primarily utilized in the synthesis of complex pharmaceutical agents, particularly in the development of protease inhibitors. Its structural features make it a valuable intermediate in the production of drugs targeting viral infections, including HIV and hepatitis C. The presence of the trifluorophenyl group enhances its binding affinity to specific enzyme targets, improving the efficacy of the final drug product. Additionally, the tert-butyl carbamate moiety provides stability during sy

This compound is primarily utilized in the synthesis of complex pharmaceutical agents, particularly in the development of protease inhibitors. Its structural features make it a valuable intermediate in the production of drugs targeting viral infections, including HIV and hepatitis C. The presence of the trifluorophenyl group enhances its binding affinity to specific enzyme targets, improving the efficacy of the final drug product. Additionally, the tert-butyl carbamate moiety provides stability during synthetic processes, ensuring the integrity of the compound in multi-step reactions. Its application is critical in medicinal chemistry for creating potent and selective therapeutic agents.

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