2-(tert-Butoxycarbonyl)-6-chloronicotinic acid

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Reagent Code: #148591
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CAS Number 1224194-44-8

science Other reagents with same CAS 1224194-44-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.67 g/mol
Formula C₁₁H₁₂ClNO₄
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

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 structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for building blocks in drug discovery programs, especially in the preparation of nicotinic acid derivatives with potential anti-inflammatory, anticancer, or antiviral properties. The Boc-protected group enables controlled deprotection and coupling reactions, facilitating peptide-like bond formation in multi-step organic syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,450.00
250mg
10-20 days ฿7,470.00
1g
10-20 days ฿16,630.00
5g
10-20 days ฿71,640.00

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2-(tert-Butoxycarbonyl)-6-chloronicotinic acid
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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 structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for building blocks in drug discovery programs, especially in the preparation of nicotinic acid derivatives with potential anti-inflammatory, anticancer, or antiviral properties. The Bo

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for building blocks in drug discovery programs, especially in the preparation of nicotinic acid derivatives with potential anti-inflammatory, anticancer, or antiviral properties. The Boc-protected group enables controlled deprotection and coupling reactions, facilitating peptide-like bond formation in multi-step organic syntheses.

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