2-Chloro-5,7-difluoroquinoline-3-carbaldehyde

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Reagent Code: #42917
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CAS Number 956631-90-6

science Other reagents with same CAS 956631-90-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.6000 g/mol
Formula C₁₀H₄ClF₂NO
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MDL Number MFCD26399738
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Storage room temperature

description Product Description

This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the development of pharmaceutical intermediates. Its unique structure makes it a valuable building block for creating molecules with potential biological activity, such as antimicrobial or anticancer agents. Researchers often employ it in the design of quinoline-based drugs, leveraging its reactive aldehyde group for further functionalization. Additionally, it serves as a key precursor in the production of fluorescent dyes and sensors due to its ability to form stable conjugated systems. Its applications extend to material science, where it contributes to the development of advanced organic materials with specific optical or electronic properties.

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Test Parameter Specification
Appearance solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,133.00

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2-Chloro-5,7-difluoroquinoline-3-carbaldehyde
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This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the development of pharmaceutical intermediates. Its unique structure makes it a valuable building block for creating molecules with potential biological activity, such as antimicrobial or anticancer agents. Researchers often employ it in the design of quinoline-based drugs, leveraging its reactive aldehyde group for further functionalization. Additionally, it serves as a key precursor in the production of

This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the development of pharmaceutical intermediates. Its unique structure makes it a valuable building block for creating molecules with potential biological activity, such as antimicrobial or anticancer agents. Researchers often employ it in the design of quinoline-based drugs, leveraging its reactive aldehyde group for further functionalization. Additionally, it serves as a key precursor in the production of fluorescent dyes and sensors due to its ability to form stable conjugated systems. Its applications extend to material science, where it contributes to the development of advanced organic materials with specific optical or electronic properties.

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