tert-butyl 8-amino-5-oxa-2-azaspiro[3.4]octane-2-carboxylate

95%

Reagent Code: #242372
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CAS Number 1408074-44-1

science Other reagents with same CAS 1408074-44-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.29 g/mol
Formula C₁₁H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD23105956
thermostat Physical Properties
Boiling Point 331.2±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its spirocyclic structure and functional groups make it valuable for constructing complex molecules with high selectivity and potency. Commonly employed in medicinal chemistry for designing kinase inhibitors and neuroactive compounds. The tert-butyl carbamate (Boc) group allows for easy protection of the amine during multi-step syntheses, enabling controlled reactivity and improved yield in drug manufacturing processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿45,380.00

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tert-butyl 8-amino-5-oxa-2-azaspiro[3.4]octane-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its spirocyclic structure and functional groups make it valuable for constructing complex molecules with high selectivity and potency. Commonly employed in medicinal chemistry for designing kinase inhibitors and neuroactive compounds. The tert-butyl carbamate (Boc) group allows for easy protection of the amine during multi-step syntheses, enabling controlled reactivity a

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its spirocyclic structure and functional groups make it valuable for constructing complex molecules with high selectivity and potency. Commonly employed in medicinal chemistry for designing kinase inhibitors and neuroactive compounds. The tert-butyl carbamate (Boc) group allows for easy protection of the amine during multi-step syntheses, enabling controlled reactivity and improved yield in drug manufacturing processes.

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