6-Bromo-2-chloro-3-methylquinoline

95%

Reagent Code: #151430
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CAS Number 113092-96-9

science Other reagents with same CAS 113092-96-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.53 g/mol
Formula C₁₀H₇BrClN
badge Registry Numbers
MDL Number MFCD02684154
thermostat Physical Properties
Melting Point 144-145 °C
Boiling Point 342.2±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.591±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antimalarial agents. Its halogenated quinoline structure allows for selective cross-coupling reactions, enabling the construction of complex bioactive molecules. Commonly employed in research settings for drug discovery due to its reactivity and ability to serve as a building block in heterocyclic chemistry. Also utilized in the preparation of fluorescent probes and materials for organic electronics owing to the quinoline core’s photophysical properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,800.00
inventory 250mg
10-20 days ฿3,030.00
inventory 1g
10-20 days ฿9,630.00
inventory 5g
10-20 days ฿41,740.00

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6-Bromo-2-chloro-3-methylquinoline
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antimalarial agents. Its halogenated quinoline structure allows for selective cross-coupling reactions, enabling the construction of complex bioactive molecules. Commonly employed in research settings for drug discovery due to its reactivity and ability to serve as a building block in heterocyclic chemistry. Also utilized in the preparation of fluorescent probes and materials for organic
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antimalarial agents. Its halogenated quinoline structure allows for selective cross-coupling reactions, enabling the construction of complex bioactive molecules. Commonly employed in research settings for drug discovery due to its reactivity and ability to serve as a building block in heterocyclic chemistry. Also utilized in the preparation of fluorescent probes and materials for organic electronics owing to the quinoline core’s photophysical properties.
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