(S)-1-(tert-Butoxycarbonyl)-3-methylpyrrolidine-3-carboxylic acid

95%

Reagent Code: #113672
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CAS Number 1821775-99-8

science Other reagents with same CAS 1821775-99-8

blur_circular Chemical Specifications

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Weight 229.27 g/mol
Formula C₁₁H₁₉NO₄
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

(S)-1-(tert-Butoxycarbonyl)-3-methylpyrrolidine-3-carboxylic acid is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it particularly valuable in the production of enantiomerically pure compounds, which are essential for developing drugs with high specificity and reduced side effects. This compound is often employed in the preparation of protease inhibitors, which are crucial in treating diseases such as HIV/AIDS and hepatitis C. Additionally, it serves as a building block in the synthesis of complex molecules for neurological and cardiovascular drugs, where precise stereochemistry is critical for efficacy. Its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it a versatile reagent in multi-step organic synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,004.00
inventory 1g
10-20 days ฿33,570.00

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(S)-1-(tert-Butoxycarbonyl)-3-methylpyrrolidine-3-carboxylic acid
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(S)-1-(tert-Butoxycarbonyl)-3-methylpyrrolidine-3-carboxylic acid is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it particularly valuable in the production of enantiomerically pure compounds, which are essential for developing drugs with high specificity and reduced side effects. This compound is often employed in the preparation of protease inhibitors, which are crucial in treating diseases such as HIV/AIDS and hepatitis C. Additionally, it serves as a building block in the synthesis of complex molecules for neurological and cardiovascular drugs, where precise stereochemistry is critical for efficacy. Its tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it a versatile reagent in multi-step organic synthesis.
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