3-((tert-Butoxycarbonyl)amino)quinoline-7-carboxylic acid

98%

Reagent Code: #130112
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CAS Number 2708280-69-5

science Other reagents with same CAS 2708280-69-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.3 g/mol
Formula C₁₅H₁₆N₂O₄
thermostat Physical Properties
Boiling Point 425.2±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.320±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in medicinal chemistry for creating targeted therapies. Commonly employed in solid-phase and solution-phase peptide-like synthesis due to the presence of both carboxylic acid and protected amine functionalities. Also utilized in the preparation of fluorescent probes and bioactive molecules where quinoline derivatives exhibit favorable optical and biological properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,700.00
inventory 250mg
10-20 days ฿33,000.00

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3-((tert-Butoxycarbonyl)amino)quinoline-7-carboxylic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in medicinal chemistry for creating targeted therapies. Commonly employed in solid-phase and solution-phase peptide-like synthesis due to the presence of both carboxylic acid and protected amine functionalities. Also utilized in the preparation of fluorescent probes and bioactive molecules where

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in medicinal chemistry for creating targeted therapies. Commonly employed in solid-phase and solution-phase peptide-like synthesis due to the presence of both carboxylic acid and protected amine functionalities. Also utilized in the preparation of fluorescent probes and bioactive molecules where quinoline derivatives exhibit favorable optical and biological properties.

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