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

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Reagent Code: #36764
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CAS Number 1430105-52-4

science Other reagents with same CAS 1430105-52-4

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Weight 277.26 g/mol
Formula C₁₂H₁₇F₂NO₄
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MDL Number MFCD28556951
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description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its unique spirocyclic structure and functional groups make it valuable for constructing biologically active compounds, especially those targeting neurological and metabolic disorders. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during multi-step synthesis, while the difluoro and carboxylic acid groups enhance the molecule's reactivity and potential for further derivatization. It is often employed in medicinal chemistry research to explore new drug candidates with improved efficacy and safety profiles.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿7,155.00

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(3R,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, particularly in the development of active pharmaceutical ingredients (APIs). Its unique spirocyclic structure and functional groups make it valuable for constructing biologically active compounds, especially those targeting neurological and metabolic disorders. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during multi-step synthesis, whil

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its unique spirocyclic structure and functional groups make it valuable for constructing biologically active compounds, especially those targeting neurological and metabolic disorders. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions during multi-step synthesis, while the difluoro and carboxylic acid groups enhance the molecule's reactivity and potential for further derivatization. It is often employed in medicinal chemistry research to explore new drug candidates with improved efficacy and safety profiles.

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