6-Bromo-2-chloroquinoline-4-carboxylic acid

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Reagent Code: #49867
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CAS Number 287176-62-9

science Other reagents with same CAS 287176-62-9

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Weight 286.5200 g/mol
Formula C₁₀H₅BrClNO₂
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MDL Number MFCD00106420
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6-Bromo-2-chloroquinoline-4-carboxylic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of quinoline-based drugs. Its structure is valuable for creating molecules with potential antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it is utilized in the design of chemical probes and ligands for studying biological targets and pathways. The compound's reactivity and functional groups make it a versatile building block in medicinal chemistry and drug discovery efforts.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,228.00

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6-Bromo-2-chloroquinoline-4-carboxylic acid
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6-Bromo-2-chloroquinoline-4-carboxylic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of quinoline-based drugs. Its structure is valuable for creating molecules with potential antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it is utilized in the design of chemical probes and ligands for studying biological targets and

6-Bromo-2-chloroquinoline-4-carboxylic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of quinoline-based drugs. Its structure is valuable for creating molecules with potential antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it is utilized in the design of chemical probes and ligands for studying biological targets and pathways. The compound's reactivity and functional groups make it a versatile building block in medicinal chemistry and drug discovery efforts.

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