2-Oxa-6,9-diazaspiro[4.5]decane-6-carboxylic acid, 1,1-dimethylethyl ester

≥95%

Reagent Code: #221072
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CAS Number 1784402-13-6

science Other reagents with same CAS 1784402-13-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.3147 g/mol
Formula C₁₂H₂₂N₂O₃
thermostat Physical Properties
Boiling Point 348.6±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.13±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its spirocyclic structure and protected functional groups make it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to build drug candidates targeting cancer, inflammation, and central nervous system disorders. The tert-butyl ester group allows for selective deprotection, enabling stepwise synthesis in multi-stage reactions.

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inventory 100mg
10-20 days ฿48,000.00

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2-Oxa-6,9-diazaspiro[4.5]decane-6-carboxylic acid, 1,1-dimethylethyl ester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its spirocyclic structure and protected functional groups make it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to build drug candidates targeting cancer, inflammation, and central nervous system disorders. The tert-butyl ester group allows for selective deprotection, enab

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its spirocyclic structure and protected functional groups make it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to build drug candidates targeting cancer, inflammation, and central nervous system disorders. The tert-butyl ester group allows for selective deprotection, enabling stepwise synthesis in multi-stage reactions.

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