6-(2-(tert-Butoxycarbonyl)hydrazinyl)nicotinic acid

95%

Reagent Code: #146066
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CAS Number 133081-25-1

science Other reagents with same CAS 133081-25-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.25 g/mol
Formula C₁₁H₁₅N₃O₄
badge Registry Numbers
MDL Number MFCD03788696
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. The tert-butoxycarbonyl (Boc)-protected hydrazine and carboxylic acid functional groups allow for versatile coupling reactions after selective deprotection under mild acidic conditions, making it valuable in medicinal chemistry for constructing heterocyclic systems. Commonly employed in solid-phase peptide synthesis and as a building block in the preparation of nicotinoyl-based derivatives with potential antiviral or anticancer activity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿154.00
inventory 250mg
10-20 days ฿1,050.00
inventory 1g
10-20 days ฿2,500.00
inventory 5g
10-20 days ฿8,280.00

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6-(2-(tert-Butoxycarbonyl)hydrazinyl)nicotinic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. The tert-butoxycarbonyl (Boc)-protected hydrazine and carboxylic acid functional groups allow for versatile coupling reactions after selective deprotection under mild acidic conditions, making it valuable in medicinal chemistry for constructing heterocyclic systems. Commonly employed in solid-phase peptide synthesis and as a building block in the prepar

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. The tert-butoxycarbonyl (Boc)-protected hydrazine and carboxylic acid functional groups allow for versatile coupling reactions after selective deprotection under mild acidic conditions, making it valuable in medicinal chemistry for constructing heterocyclic systems. Commonly employed in solid-phase peptide synthesis and as a building block in the preparation of nicotinoyl-based derivatives with potential antiviral or anticancer activity.

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