6-Bromo-4-chloroquinazoline

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Reagent Code: #145463
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CAS Number 38267-96-8

science Other reagents with same CAS 38267-96-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.49 g/mol
Formula C₈H₄BrClN₂
thermostat Physical Properties
Boiling Point 339.7°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive halogen sites, allowing for selective cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Commonly employed in research settings to design and optimize bioactive molecules targeting tyrosine kinase pathways. Also explored in agrochemical research for developing novel pesticidal agents. Its structure supports the creation of diverse quinazoline derivatives with potential antitumor, anti-inflammatory, and antimicrobial activities.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿980.00
inventory 10g
10-20 days ฿1,920.00

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6-Bromo-4-chloroquinazoline
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive halogen sites, allowing for selective cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Commonly employed in research settings to design and optimize bioactive molecules targeting tyrosine kinase pathways. Also explored in agrochemical research for developing novel pes

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its reactive halogen sites, allowing for selective cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Commonly employed in research settings to design and optimize bioactive molecules targeting tyrosine kinase pathways. Also explored in agrochemical research for developing novel pesticidal agents. Its structure supports the creation of diverse quinazoline derivatives with potential antitumor, anti-inflammatory, and antimicrobial activities.

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