Ethyl 5-((tert-butoxycarbonyl)amino)-6-methylnicotinate

≥95%

Reagent Code: #184499
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CAS Number 936801-42-2

science Other reagents with same CAS 936801-42-2

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scatter_plot Molecular Information
Weight 280.32 g/mol
Formula C₁₄H₂₀N₂O₄
badge Registry Numbers
MDL Number MFCD18256584
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

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 pyridine-based structure (a substituted nicotinate) supports the construction of nitrogen-containing heterocycles, which are common in drug design. The Boc-protected amine group allows for selective deprotection and further functionalization, while the ethyl ester can be hydrolyzed to the carboxylic acid or converted to amides, enhancing versatility in multi-step organic syntheses, especially in medicinal chemistry research. Commonly employed in the preparation of potential anti-inflammatory, anticancer, and antiviral agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿30,660.00
inventory 250mg
10-20 days ฿55,580.00

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Ethyl 5-((tert-butoxycarbonyl)amino)-6-methylnicotinate
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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 pyridine-based structure (a substituted nicotinate) supports the construction of nitrogen-containing heterocycles, which are common in drug design. The Boc-protected amine group allows for selective deprotection and further functionalization, while the ethyl ester can be hydrolyzed to the carboxylic acid or converted to amides, enhancing v

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its pyridine-based structure (a substituted nicotinate) supports the construction of nitrogen-containing heterocycles, which are common in drug design. The Boc-protected amine group allows for selective deprotection and further functionalization, while the ethyl ester can be hydrolyzed to the carboxylic acid or converted to amides, enhancing versatility in multi-step organic syntheses, especially in medicinal chemistry research. Commonly employed in the preparation of potential anti-inflammatory, anticancer, and antiviral agents.

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