Ethyl 6-((tert-butoxycarbonyl)amino)spiro[3.3]heptane-2-carboxylate

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Reagent Code: #75694
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CAS Number 1272412-66-4

science Other reagents with same CAS 1272412-66-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.36 g/mol
Formula C₁₅H₂₅NO₄
badge Registry Numbers
MDL Number MFCD17016158
inventory_2 Storage & Handling
Storage 2-8°C, sealed and dry

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a spirocyclic framework, makes it valuable in the synthesis of pharmaceuticals and bioactive compounds. The Boc group is often employed to protect amine functionalities during multi-step reactions, allowing selective transformations elsewhere in the molecule. Additionally, the spiro[3.3]heptane core contributes unique steric and electronic properties, which can enhance the stability or activity of the target molecules. This chemical is particularly useful in medicinal chemistry for designing drug candidates with improved pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿83,448.00
inventory 1g
10-20 days ฿27,945.00

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Ethyl 6-((tert-butoxycarbonyl)amino)spiro[3.3]heptane-2-carboxylate
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This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a spirocyclic framework, makes it valuable in the synthesis of pharmaceuticals and bioactive compounds. The Boc group is often employed to protect amine functionalities during multi-step reactions, allowing selective transformations elsewhere in the molecule. Additionally, the spiro[3.3]heptane core contri

This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a spirocyclic framework, makes it valuable in the synthesis of pharmaceuticals and bioactive compounds. The Boc group is often employed to protect amine functionalities during multi-step reactions, allowing selective transformations elsewhere in the molecule. Additionally, the spiro[3.3]heptane core contributes unique steric and electronic properties, which can enhance the stability or activity of the target molecules. This chemical is particularly useful in medicinal chemistry for designing drug candidates with improved pharmacokinetic properties.

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