N-((8-Hydroxyquinolin-7-yl)(thiophen-2-yl)methyl)butyramide

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Reagent Code: #245661
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CAS Number 332939-32-9

science Other reagents with same CAS 332939-32-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 326.41 g/mol
Formula C₁₈H₁₈N₂O₂S
thermostat Physical Properties
Boiling Point 607.8±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.271±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in research as a potential metal chelating agent due to the presence of hydroxyquinoline and amide functionalities, enabling selective binding to transition metals. This property makes it suitable for applications in sensing systems, particularly in the development of fluorescent probes for detecting metal ions in environmental or biological samples. Also explored for its antimicrobial and anticancer activities in pharmaceutical studies, where the conjugated structure enhances cell permeability and bioactivity. Additionally, serves as an intermediate in synthesizing more complex heterocyclic compounds for materials science and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿5,660.00
inventory 50mg
10-20 days ฿18,130.00

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N-((8-Hydroxyquinolin-7-yl)(thiophen-2-yl)methyl)butyramide
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Used in research as a potential metal chelating agent due to the presence of hydroxyquinoline and amide functionalities, enabling selective binding to transition metals. This property makes it suitable for applications in sensing systems, particularly in the development of fluorescent probes for detecting metal ions in environmental or biological samples. Also explored for its antimicrobial and anticancer activities in pharmaceutical studies, where the conjugated structure enhances cell permeability and

Used in research as a potential metal chelating agent due to the presence of hydroxyquinoline and amide functionalities, enabling selective binding to transition metals. This property makes it suitable for applications in sensing systems, particularly in the development of fluorescent probes for detecting metal ions in environmental or biological samples. Also explored for its antimicrobial and anticancer activities in pharmaceutical studies, where the conjugated structure enhances cell permeability and bioactivity. Additionally, serves as an intermediate in synthesizing more complex heterocyclic compounds for materials science and medicinal chemistry.

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