6-Bromo-3-fluoroquinoline

95%

Reagent Code: #87659
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CAS Number 1355583-13-9

science Other reagents with same CAS 1355583-13-9

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scatter_plot Molecular Information
Weight 226.05 g/mol
Formula C₉H₅BrFN
badge Registry Numbers
MDL Number MFCD22690571
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

6-Bromo-3-fluoroquinoline is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the creation of quinoline-based drugs, which are known for their broad therapeutic applications. The compound is often utilized in the design of antimicrobial and anticancer agents due to the inherent biological activity of the quinoline scaffold. Additionally, it serves as a building block in the development of fluorescent probes and imaging agents, aiding in the study of cellular processes and disease mechanisms. Its halogenated nature allows for further chemical modifications, making it a versatile component in medicinal chemistry and drug discovery efforts.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,744.00
inventory 250mg
10-20 days ฿19,080.00

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6-Bromo-3-fluoroquinoline
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6-Bromo-3-fluoroquinoline is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the creation of quinoline-based drugs, which are known for their broad therapeutic applications. The compound is often utilized in the design of antimicrobial and anticancer agents due to the inherent biological activity of the quinoline scaffold. Additionally, it serves as a building block in the

6-Bromo-3-fluoroquinoline is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the creation of quinoline-based drugs, which are known for their broad therapeutic applications. The compound is often utilized in the design of antimicrobial and anticancer agents due to the inherent biological activity of the quinoline scaffold. Additionally, it serves as a building block in the development of fluorescent probes and imaging agents, aiding in the study of cellular processes and disease mechanisms. Its halogenated nature allows for further chemical modifications, making it a versatile component in medicinal chemistry and drug discovery efforts.

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