tert-Butyl (5-methylisoxazol-3-yl)carbamate

95%

Reagent Code: #150828
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CAS Number 97517-66-3

science Other reagents with same CAS 97517-66-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.22 g/mol
Formula C₉H₁₄N₂O₃
badge Registry Numbers
MDL Number MFCD11976787
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) featuring isoxazole moieties. It serves as a protected amine derivative, enabling selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing kinase inhibitors and other bioactive molecules where the isoxazole ring acts as a heterocyclic scaffold. Its tert-butoxycarbonyl (Boc) group allows for easy deprotection under mild acidic conditions, making it valuable in peptide-like coupling strategies and combinatorial chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,330.00
inventory 250mg
10-20 days ฿26,830.00
inventory 1g
10-20 days ฿53,660.00

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tert-Butyl (5-methylisoxazol-3-yl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) featuring isoxazole moieties. It serves as a protected amine derivative, enabling selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing kinase inhibitors and other bioactive molecules where the isoxazole ring acts as a heterocyclic scaffold. Its tert-butoxycarbonyl (Boc) group allows for easy deprotection

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) featuring isoxazole moieties. It serves as a protected amine derivative, enabling selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing kinase inhibitors and other bioactive molecules where the isoxazole ring acts as a heterocyclic scaffold. Its tert-butoxycarbonyl (Boc) group allows for easy deprotection under mild acidic conditions, making it valuable in peptide-like coupling strategies and combinatorial chemistry.

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