1-(tert-Butoxycarbonyl)azetidine-2-carboxylic acid

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Reagent Code: #144670
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CAS Number 159749-28-7

science Other reagents with same CAS 159749-28-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.22 g/mol
Formula C₉H₁₅NO₄
badge Registry Numbers
MDL Number MFCD01861756
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules and drug candidates. Its protected azetidine ring serves as a structural motif in medicinal chemistry, offering conformational rigidity and improved metabolic stability. Commonly employed in peptide-like structures and heterocyclic compounds, it facilitates the construction of complex molecules for research in oncology, CNS disorders, and infectious diseases. Also utilized in solid-phase and solution-phase synthesis due to its compatibility with various coupling reagents and protecting group strategies.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿650.00
inventory 5g
10-20 days ฿2,800.00

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1-(tert-Butoxycarbonyl)azetidine-2-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules and drug candidates. Its protected azetidine ring serves as a structural motif in medicinal chemistry, offering conformational rigidity and improved metabolic stability. Commonly employed in peptide-like structures and heterocyclic compounds, it facilitates the construction of complex molecules for research in oncology, CNS disorders, and infectious diseases. Also utilize
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules and drug candidates. Its protected azetidine ring serves as a structural motif in medicinal chemistry, offering conformational rigidity and improved metabolic stability. Commonly employed in peptide-like structures and heterocyclic compounds, it facilitates the construction of complex molecules for research in oncology, CNS disorders, and infectious diseases. Also utilized in solid-phase and solution-phase synthesis due to its compatibility with various coupling reagents and protecting group strategies.
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