6-Bromoquinazoline-4-carbonitrile

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Reagent Code: #81537
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CAS Number 1204334-27-9

science Other reagents with same CAS 1204334-27-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.06 g/mol
Formula C₉H₄BrN₃
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of quinazoline-based compounds, which are known for their potential therapeutic applications. It serves as a building block in the creation of inhibitors targeting specific enzymes, such as tyrosine kinases, which play a critical role in cell signaling and cancer progression. Additionally, it is employed in the preparation of compounds with potential anti-inflammatory, antiviral, and antimicrobial properties, making it a versatile tool in drug discovery and development. Its reactive bromo and cyano groups allow for further functionalization, enabling the design of diverse chemical libraries for screening and optimization.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,203.00
inventory 250mg
10-20 days ฿12,672.00

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6-Bromoquinazoline-4-carbonitrile
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This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of quinazoline-based compounds, which are known for their potential therapeutic applications. It serves as a building block in the creation of inhibitors targeting specific enzymes, such as tyrosine kinases, which play a critical role in cell signaling and cancer progression. Ad

This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of quinazoline-based compounds, which are known for their potential therapeutic applications. It serves as a building block in the creation of inhibitors targeting specific enzymes, such as tyrosine kinases, which play a critical role in cell signaling and cancer progression. Additionally, it is employed in the preparation of compounds with potential anti-inflammatory, antiviral, and antimicrobial properties, making it a versatile tool in drug discovery and development. Its reactive bromo and cyano groups allow for further functionalization, enabling the design of diverse chemical libraries for screening and optimization.

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