tert-Butyl 2-hydroxy-6-azaspiro[3.4]octane-6-carboxylate

95%

Reagent Code: #75339
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CAS Number 1239319-91-5

science Other reagents with same CAS 1239319-91-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.3 g/mol
Formula C₁₂H₂₁NO₃
badge Registry Numbers
MDL Number MFCD18073249
thermostat Physical Properties
Boiling Point 338℃ at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed and dry

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of complex molecules, often contributing to the construction of spirocyclic structures, which are valuable in drug discovery. Its unique spiro[3.4]octane framework makes it a versatile building block for designing compounds with potential biological activity. Additionally, it is employed in research settings to explore novel therapeutic agents, especially in the areas of central nervous system disorders and metabolic diseases. The tert-butyl and carboxylate groups enhance its stability and reactivity, facilitating its use in multi-step synthetic processes.

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Test Parameter Specification
Appearance Yellow viscous liquid
Purity (%) 94.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,414.00
inventory 5g
10-20 days ฿27,459.00

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tert-Butyl 2-hydroxy-6-azaspiro[3.4]octane-6-carboxylate
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This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the production of complex molecules, often contributing to the construction of spirocyclic structures, which are valuable in drug discovery. Its unique spiro[3.4]octane framework makes it a versatile building block for designing compounds with potential biological activity. Additionally, it is employed in research settings to explore novel therapeutic agents, especially in the areas of central nervous system disorders and metabolic diseases. The tert-butyl and carboxylate groups enhance its stability and reactivity, facilitating its use in multi-step synthetic processes.
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