6-Bromo-3-iodoquinolin-4-ol

≥95%

Reagent Code: #85559
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CAS Number 1260886-58-5

science Other reagents with same CAS 1260886-58-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 349.95 g/mol
Formula C₉H₅BrINO
badge Registry Numbers
MDL Number MFCD15527294
inventory_2 Storage & Handling
Storage Room temperature, dark, inert gas

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the construction of more complex quinoline derivatives. Its unique structure, featuring both bromo and iodo substituents, makes it a valuable precursor for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are widely employed in pharmaceutical and material science research. Additionally, it is often used in the development of biologically active compounds, particularly in the synthesis of potential drug candidates targeting various diseases, including cancer and infectious diseases. Its role in the preparation of fluorescent dyes and sensors is also noteworthy, as it contributes to advancements in analytical chemistry and bioimaging techniques.

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Test Parameter Specification
Appearance Off-White Solid
Purity (%) 95-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,791.00
inventory 250mg
10-20 days ฿3,060.00
inventory 1g
10-20 days ฿8,289.00

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6-Bromo-3-iodoquinolin-4-ol
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the construction of more complex quinoline derivatives. Its unique structure, featuring both bromo and iodo substituents, makes it a valuable precursor for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are widely employed in pharmaceutical and material science research. Additionally, it is often used in the development of biologically active compounds, particul

This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the construction of more complex quinoline derivatives. Its unique structure, featuring both bromo and iodo substituents, makes it a valuable precursor for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are widely employed in pharmaceutical and material science research. Additionally, it is often used in the development of biologically active compounds, particularly in the synthesis of potential drug candidates targeting various diseases, including cancer and infectious diseases. Its role in the preparation of fluorescent dyes and sensors is also noteworthy, as it contributes to advancements in analytical chemistry and bioimaging techniques.

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