(3S,6S)-5-(tert-Butoxycarbonyl)-1,1-difluoro-5-azaspiro[2.4]heptane-6-carboxylic acid

97%

Reagent Code: #70924
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CAS Number 1980007-35-9

science Other reagents with same CAS 1980007-35-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.26 g/mol
Formula C₁₂H₁₇F₂NO₄
badge Registry Numbers
MDL Number MFCD28396445
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic molecules. Its unique spirocyclic structure and functional groups make it valuable for constructing biologically active compounds, particularly in the development of novel drugs targeting specific enzymes or receptors. The tert-butoxycarbonyl (Boc) protecting group ensures stability during synthetic processes, while the difluoro and carboxylic acid moieties enhance reactivity and enable further derivatization. It is commonly employed in medicinal chemistry research to create potential therapeutic agents, especially in areas like central nervous system disorders or metabolic diseases. Its structural features also make it suitable for use in peptide mimetics, where it can mimic natural peptide structures to improve drug efficacy and stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,640.00
inventory 250mg
10-20 days ฿34,060.00

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(3S,6S)-5-(tert-Butoxycarbonyl)-1,1-difluoro-5-azaspiro[2.4]heptane-6-carboxylic acid
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This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic molecules. Its unique spirocyclic structure and functional groups make it valuable for constructing biologically active compounds, particularly in the development of novel drugs targeting specific enzymes or receptors. The tert-butoxycarbonyl (Boc) protecting group ensures stability during synthetic processes, while the difluoro and carboxylic acid moieties enhance reactivity and enable further derivatization. It is commonly employed in medicinal chemistry research to create potential therapeutic agents, especially in areas like central nervous system disorders or metabolic diseases. Its structural features also make it suitable for use in peptide mimetics, where it can mimic natural peptide structures to improve drug efficacy and stability.
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