tert-Butyl ((3-oxocyclobutyl)methyl)carbamate

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Reagent Code: #150201
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CAS Number 130369-09-4

science Other reagents with same CAS 130369-09-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.25 g/mol
Formula C₁₀H₁₇NO₃
badge Registry Numbers
MDL Number MFCD11499004
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. The tert-butyl carbamate group serves as a protected amine, enabling selective reactions in multi-step organic syntheses. The cyclobutyl ketone moiety allows for further functionalization, such as nucleophilic addition or ring expansion reactions, making it valuable in constructing complex molecular frameworks. Commonly employed in medicinal chemistry for optimizing lead compounds and enhancing metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,920.00
inventory 250mg
10-20 days ฿3,200.00
inventory 1g
10-20 days ฿5,520.00
inventory 5g
10-20 days ฿20,800.00
inventory 25g
10-20 days ฿67,200.00

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tert-Butyl ((3-oxocyclobutyl)methyl)carbamate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. The tert-butyl carbamate group serves as a protected amine, enabling selective reactions in multi-step organic syntheses. The cyclobutyl ketone moiety allows for further functionalization, such as nucleophilic addition or ring expansion reactions, making it valuable in constructing complex molecular frameworks. Commonly employed in medicinal chemistry for optimizing lead compou

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. The tert-butyl carbamate group serves as a protected amine, enabling selective reactions in multi-step organic syntheses. The cyclobutyl ketone moiety allows for further functionalization, such as nucleophilic addition or ring expansion reactions, making it valuable in constructing complex molecular frameworks. Commonly employed in medicinal chemistry for optimizing lead compounds and enhancing metabolic stability.

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