3-bromoquinolin-5-amine

≥95%

Reagent Code: #144062
label
Alias 3-Bromoquinoline-5-amine
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CAS Number 116632-57-6

science Other reagents with same CAS 116632-57-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.07 g/mol
Formula C₉H₇BrN₂
badge Registry Numbers
MDL Number MFCD20327979
thermostat Physical Properties
Boiling Point 352.5±27.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.649±0.06 g/cm3(Predicted)
Storage Room temperature, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure allows for functionalization in multi-step reactions, making it valuable in medicinal chemistry for building nitrogen-containing heterocyclic systems. Also employed in the preparation of fluorescent dyes and sensors due to its quinoline backbone, which exhibits favorable photophysical properties. Commonly utilized in research settings for generating compound libraries in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿850.00

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3-bromoquinolin-5-amine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure allows for functionalization in multi-step reactions, making it valuable in medicinal chemistry for building nitrogen-containing heterocyclic systems. Also employed in the preparation of fluorescent dyes and sensors due to its quinoline backbone, which exhibits favorable photophysical properties. Commonly utilized in research settings for generating

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure allows for functionalization in multi-step reactions, making it valuable in medicinal chemistry for building nitrogen-containing heterocyclic systems. Also employed in the preparation of fluorescent dyes and sensors due to its quinoline backbone, which exhibits favorable photophysical properties. Commonly utilized in research settings for generating compound libraries in drug discovery programs.

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