3-Bromo-8-(trifluoromethyl)quinoline

98%

Reagent Code: #151196
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CAS Number 1059064-11-7

science Other reagents with same CAS 1059064-11-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.05 g/mol
Formula C₁₀H₅BrF₃N
badge Registry Numbers
MDL Number MFCD25542362
thermostat Physical Properties
Boiling Point 284.0±35.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a building block in the development of bioactive molecules. Its halogen and trifluoromethyl functional groups enable cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex quinoline derivatives. It is also employed in research for designing kinase inhibitors and compounds with antiparasitic or anticancer activity. Additionally, it finds use in the preparation of ligands for catalysis and in materials science for developing fluorinated organic semiconductors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,320.00
inventory 250mg
10-20 days ฿15,470.00
inventory 1g
10-20 days ฿53,710.00

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3-Bromo-8-(trifluoromethyl)quinoline
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a building block in the development of bioactive molecules. Its halogen and trifluoromethyl functional groups enable cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex quinoline derivatives. It is also employed in research for designing kinase inhibitors and compounds with antiparasitic or anticancer activity. Additionally, it finds use in the preparat

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a building block in the development of bioactive molecules. Its halogen and trifluoromethyl functional groups enable cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex quinoline derivatives. It is also employed in research for designing kinase inhibitors and compounds with antiparasitic or anticancer activity. Additionally, it finds use in the preparation of ligands for catalysis and in materials science for developing fluorinated organic semiconductors.

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