Carbamicacid,[(3S)-1-[[[3-(trifluoromethyl)benzoyl]amino]acetyl]-3-pyrrolidinyl]-,1,1-dimethylethylester

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Reagent Code: #166555
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CAS Number 857650-89-6

science Other reagents with same CAS 857650-89-6

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Weight 415.41 g/mol
Formula C₁₉H₂₄F₃N₃O₄
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 protease inhibitors and antiviral agents. Its structure supports chiral synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in research settings for designing enzyme inhibitors due to its ability to mimic peptide bonds and interact with active sites. Also utilized in the preparation of bioactive molecules where steric protection and metabolic stability are required, thanks to the tert-butyl ester group.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,870.00
inventory 1g
10-20 days ฿80,940.00
inventory 250mg
10-20 days ฿32,980.00

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Carbamicacid,[(3S)-1-[[[3-(trifluoromethyl)benzoyl]amino]acetyl]-3-pyrrolidinyl]-,1,1-dimethylethylester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and antiviral agents. Its structure supports chiral synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in research settings for designing enzyme inhibitors due to its ability to mimic peptide bonds and interact with active sites. Also utilized in the preparation of bioactive molecules where steric protection and metabolic stability are required

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and antiviral agents. Its structure supports chiral synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in research settings for designing enzyme inhibitors due to its ability to mimic peptide bonds and interact with active sites. Also utilized in the preparation of bioactive molecules where steric protection and metabolic stability are required, thanks to the tert-butyl ester group.

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