5-(TERT-BUTOXYCARBONYL)-5-AZASPIRO[2.3]HEXANE-1-CARBOXYLIC ACID

95%

Reagent Code: #75644
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CAS Number 1251012-82-4

science Other reagents with same CAS 1251012-82-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227 g/mol
Formula C₁₁H₁₇NO₄
badge Registry Numbers
MDL Number MFCD17016192
inventory_2 Storage & Handling
Storage 2-8°C, sealed and dry

description Product Description

This compound is primarily used in organic synthesis and pharmaceutical research as a building block for the development of complex molecules. Its spirocyclic structure and tert-butoxycarbonyl (Boc) protecting group make it valuable in peptide synthesis and medicinal chemistry. It serves as an intermediate in the creation of biologically active compounds, particularly in the design of drugs targeting neurological disorders or other therapeutic areas. The Boc group provides stability during chemical reactions, allowing for selective deprotection when needed. Its application extends to the synthesis of spirocyclic scaffolds, which are increasingly explored for their potential in drug discovery due to their unique three-dimensional structure and potential for enhanced binding affinity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,490.00
inventory 250mg
10-20 days ฿5,820.00
inventory 1g
10-20 days ฿17,460.00

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5-(TERT-BUTOXYCARBONYL)-5-AZASPIRO[2.3]HEXANE-1-CARBOXYLIC ACID
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This compound is primarily used in organic synthesis and pharmaceutical research as a building block for the development of complex molecules. Its spirocyclic structure and tert-butoxycarbonyl (Boc) protecting group make it valuable in peptide synthesis and medicinal chemistry. It serves as an intermediate in the creation of biologically active compounds, particularly in the design of drugs targeting neurological disorders or other therapeutic areas. The Boc group provides stability during chemical react

This compound is primarily used in organic synthesis and pharmaceutical research as a building block for the development of complex molecules. Its spirocyclic structure and tert-butoxycarbonyl (Boc) protecting group make it valuable in peptide synthesis and medicinal chemistry. It serves as an intermediate in the creation of biologically active compounds, particularly in the design of drugs targeting neurological disorders or other therapeutic areas. The Boc group provides stability during chemical reactions, allowing for selective deprotection when needed. Its application extends to the synthesis of spirocyclic scaffolds, which are increasingly explored for their potential in drug discovery due to their unique three-dimensional structure and potential for enhanced binding affinity.

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