4-Amino-8-bromo-2-chloroquinazoline

97%

Reagent Code: #104597
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CAS Number 956100-62-2

science Other reagents with same CAS 956100-62-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.51 g/mol
Formula C₈H₅BrClN₃
badge Registry Numbers
MDL Number MFCD11858275
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure makes it a valuable intermediate in the creation of quinazoline derivatives, which are often explored for their potential therapeutic properties. Researchers focus on its application in designing molecules that target specific enzymes or receptors, particularly in the fields of oncology and infectious diseases. Additionally, it serves as a building block in medicinal chemistry for developing compounds with potential anti-cancer, anti-inflammatory, or antimicrobial activities. Its halogenated and amino-functionalized structure allows for further chemical modifications, enabling the exploration of diverse biological activities.

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Test Parameter Specification
Purity (%) 96.5-100
Appearance Solid

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,521.00
inventory 5g
10-20 days ฿5,382.00

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4-Amino-8-bromo-2-chloroquinazoline
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure makes it a valuable intermediate in the creation of quinazoline derivatives, which are often explored for their potential therapeutic properties. Researchers focus on its application in designing molecules that target specific enzymes or receptors, particularly in the fields of oncology and infectious diseases. Additionally, it serves as a building block in medicinal chemistry for developing compounds with potential anti-cancer, anti-inflammatory, or antimicrobial activities. Its halogenated and amino-functionalized structure allows for further chemical modifications, enabling the exploration of diverse biological activities.
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