5-Bromoquinoline-3-carbonitrile

98%

Reagent Code: #151466
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CAS Number 1974296-18-8

science Other reagents with same CAS 1974296-18-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.06 g/mol
Formula C₁₀H₅BrN₂
badge Registry Numbers
MDL Number MFCD31629647
thermostat Physical Properties
Boiling Point 379.7±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.66±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form biaryl and styryl derivatives with biological activity. Also utilized in the preparation of kinase inhibitors and antimicrobial compounds. Its bromine moiety facilitates metal-catalyzed transformations, enhancing its utility in drug discovery research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,230.00
inventory 250mg
10-20 days ฿33,490.00

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5-Bromoquinoline-3-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form biaryl and styryl derivatives with biological activity. Also utilized in the preparation of kinase inhibitors and antimicrobial compounds.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form biaryl and styryl derivatives with biological activity. Also utilized in the preparation of kinase inhibitors and antimicrobial compounds. Its bromine moiety facilitates metal-catalyzed transformations, enhancing its utility in drug discovery research.

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