7-Bromo-2-chloroquinazoline

95%

Reagent Code: #53984
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CAS Number 953039-66-2

science Other reagents with same CAS 953039-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.49 g/mol
Formula C₈H₄BrClN₂
badge Registry Numbers
MDL Number MFCD11040175
thermostat Physical Properties
Boiling Point 240.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

7-Bromo-2-chloroquinazoline is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure serves as a foundational scaffold for developing potential therapeutic agents, particularly in the design of kinase inhibitors. These inhibitors are crucial in targeting specific enzymes involved in signaling pathways, making it valuable for research in cancer treatment and other diseases driven by abnormal kinase activity. Additionally, it is employed in the preparation of quinazoline derivatives, which are explored for their antimicrobial, anti-inflammatory, and antitumor properties. Its versatility in chemical reactions also makes it a useful building block in organic synthesis for creating complex molecules with potential pharmaceutical applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,351.00
inventory 5g
10-20 days ฿26,730.00
inventory 100mg
10-20 days ฿1,998.00
inventory 250mg
10-20 days ฿3,987.00

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7-Bromo-2-chloroquinazoline
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7-Bromo-2-chloroquinazoline is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure serves as a foundational scaffold for developing potential therapeutic agents, particularly in the design of kinase inhibitors. These inhibitors are crucial in targeting specific enzymes involved in signaling pathways, making it valuable for research in cancer treatment and other diseases driven by abnormal kinase activity. Additionally, it is employed in the preparation of quinazoline derivatives, which are explored for their antimicrobial, anti-inflammatory, and antitumor properties. Its versatility in chemical reactions also makes it a useful building block in organic synthesis for creating complex molecules with potential pharmaceutical applications.
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