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Home  > Chemistry  > Heterocyclic Building Blocks  > Quinazolines  > 7-Bromo-2,4-dichloroquinazoline

AB70063

959237-68-4 | 7-Bromo-2,4-dichloroquinazoline

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $8.00 $5.00 -   +
250mg 95% in stock $12.00 $8.00 -   +
1g 95% in stock $26.00 $18.00 -   +
5g 95% in stock $90.00 $63.00 -   +
10g 95% in stock $168.00 $117.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB70063
Chemical Name: 7-Bromo-2,4-dichloroquinazoline
CAS Number: 959237-68-4
Molecular Formula: C8H3BrCl2N2
Molecular Weight: 277.9328
MDL Number: MFCD09954890
SMILES: Brc1ccc2c(c1)nc(nc2Cl)Cl

 

Computed Properties
Complexity: 193  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 2  
XLogP3: 4.2  

 

 

Upstream Synthesis Route
  • 7-Bromo-2,4-dichloroquinazoline is a versatile building block in chemical synthesis due to its unique structural properties. This compound is commonly utilized as a key intermediate in the development of pharmaceuticals, agrochemicals, dyes, and other specialty chemicals. Its strategic positioning of bromine and chlorine substituents makes it an ideal precursor for the synthesis of complex organic molecules with specific biological or chemical activities.In organic synthesis, 7-Bromo-2,4-dichloroquinazoline serves as a valuable starting material for introducing functional groups, facilitating diversification, and enhancing molecular complexity. Its reactivity allows chemists to perform various types of transformations, such as nucleophilic substitutions, cross-coupling reactions, and heterocyclic chemistry. By incorporating this compound into synthetic routes, researchers can access a wide range of structurally diverse compounds with potential applications in drug discovery and materials science.Additionally, the presence of bromine and chlorine atoms in 7-Bromo-2,4-dichloroquinazoline enhances its versatility as a synthetic building block. These halogens can participate in specific reactions, including halogenation, metal-catalyzed coupling reactions, and halogen-metal exchanges, enabling the rapid construction of complex molecular architectures. By harnessing the reactivity of these halogens, chemists can streamline the synthesis of target molecules and explore new avenues for chemical innovation.Overall, the strategic use of 7-Bromo-2,4-dichloroquinazoline in chemical synthesis offers a powerful tool for accessing structurally diverse compounds with potential applications in various industries. Its role as a versatile intermediate underscores its importance in modern organic synthesis, highlighting its value in the development of novel molecules with tailored properties and functionalities.
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