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

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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.

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