tert-Butyl (5-oxo-4,5-dihydropyrazin-2-yl)carbamate

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Reagent Code: #130637
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CAS Number 2733641-59-1

science Other reagents with same CAS 2733641-59-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.22 g/mol
Formula C₉H₁₃N₃O₃
inventory_2 Storage & Handling
Density 1.26±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drug design. The tert-butyl carbamate group acts as a protecting group for amines, enabling selective reactions in multi-step organic syntheses. It is also employed in the preparation of pyrazine-based compounds with potential antiviral or anticancer activity. Commonly utilized in research settings for library generation in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,050.00
inventory 1g
10-20 days ฿36,750.00
inventory 250mg
10-20 days ฿13,640.00

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tert-Butyl (5-oxo-4,5-dihydropyrazin-2-yl)carbamate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drug design. The tert-butyl carbamate group acts as a protecting group for amines, enabling selective reactions in multi-step organic syntheses. It is also employed in the preparation of pyrazine-based compounds with potential antiviral or anticancer activity. Commonly utili

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drug design. The tert-butyl carbamate group acts as a protecting group for amines, enabling selective reactions in multi-step organic syntheses. It is also employed in the preparation of pyrazine-based compounds with potential antiviral or anticancer activity. Commonly utilized in research settings for library generation in medicinal chemistry.

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