8-Bromo-4-chloro-2-(trifluoromethyl)quinoline

≥97%

Reagent Code: #173085
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CAS Number 655235-61-3

science Other reagents with same CAS 655235-61-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 310.50 g/mol
Formula C₁₀H₄BrClF₃N
badge Registry Numbers
MDL Number MFCD00174293
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. It is also employed in the preparation of bioactive quinoline derivatives with potential antimicrobial and anti-inflammatory properties. Due to the presence of reactive bromo and chloro groups, it serves as a versatile building block in Suzuki, Stille, and Buchwald-Hartwig reactions in drug discovery research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,860.00
inventory 1g
10-20 days ฿5,560.00
inventory 5g
10-20 days ฿13,920.00

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8-Bromo-4-chloro-2-(trifluoromethyl)quinoline
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. It is also employed in the preparation of bioactive quinoline derivatives with potential antimicrobial and anti-inflammatory properties. Due to the presence of reactive bromo and chloro groups, it serves

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. It is also employed in the preparation of bioactive quinoline derivatives with potential antimicrobial and anti-inflammatory properties. Due to the presence of reactive bromo and chloro groups, it serves as a versatile building block in Suzuki, Stille, and Buchwald-Hartwig reactions in drug discovery research.

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