Lithium (S)-1-(tert-butoxycarbonyl)aziridine-2-carboxylate

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Reagent Code: #37942
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CAS Number 2173637-20-0

science Other reagents with same CAS 2173637-20-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.14 g/mol
Formula C₈H₁₄LiNO₄
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MDL Number MFCD31620814
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of chiral compounds, particularly in pharmaceutical research. It plays a crucial role in the production of enantiomerically pure drugs, where precise stereochemistry is essential for biological activity. The compound is also employed in peptide synthesis, aiding in the formation of aziridine-containing peptides, which are valuable in medicinal chemistry. Additionally, it serves as a building block in the development of novel organic molecules with potential applications in material science and catalysis. Its stability and reactivity make it a versatile reagent in asymmetric synthesis.

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inventory 100mg
10-20 days ฿6,831.00

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Lithium (S)-1-(tert-butoxycarbonyl)aziridine-2-carboxylate
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Used as a key intermediate in the synthesis of chiral compounds, particularly in pharmaceutical research. It plays a crucial role in the production of enantiomerically pure drugs, where precise stereochemistry is essential for biological activity. The compound is also employed in peptide synthesis, aiding in the formation of aziridine-containing peptides, which are valuable in medicinal chemistry. Additionally, it serves as a building block in the development of novel organic molecules with potential app

Used as a key intermediate in the synthesis of chiral compounds, particularly in pharmaceutical research. It plays a crucial role in the production of enantiomerically pure drugs, where precise stereochemistry is essential for biological activity. The compound is also employed in peptide synthesis, aiding in the formation of aziridine-containing peptides, which are valuable in medicinal chemistry. Additionally, it serves as a building block in the development of novel organic molecules with potential applications in material science and catalysis. Its stability and reactivity make it a versatile reagent in asymmetric synthesis.

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