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Home  > Chemistry  > Heterocyclic Building Blocks  > Isoquinolines  > 5-Bromo-8-chloroisoquinoline

AC79355

956003-79-5 | 5-Bromo-8-chloroisoquinoline

Packsize Purity Availability Price Discounted Price    Quantity
250mg 96% in stock $251.00 $176.00 -   +
1g 96% in stock $628.00 $440.00 -   +
5g 96% in stock $1,552.00 $1,086.00 -   +
10g 96% in stock $2,625.00 $1,837.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AC79355
Chemical Name: 5-Bromo-8-chloroisoquinoline
CAS Number: 956003-79-5
Molecular Formula: C9H5BrClN
Molecular Weight: 242.4997
MDL Number: MFCD07644623
SMILES: Clc1ccc(c2c1cncc2)Br

 

Computed Properties
Complexity: 165  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 1  
XLogP3: 3.4  

 

 

Upstream Synthesis Route
  • 5-Bromo-8-chloroisoquinoline, a versatile chemical compound, acts as a key building block in the realm of chemical synthesis due to its unique structural features and reactivity. With a bromine atom at the 5-position and a chlorine atom at the 8-position on the isoquinoline ring, this compound offers a diverse range of synthetic pathways and applications.In organic synthesis, 5-Bromo-8-chloroisoquinoline serves as a valuable intermediate for the preparation of various biologically active compounds and pharmaceuticals. Its strategic positioning of halogen atoms facilitates further functionalization through substitution reactions, enabling the introduction of different chemical groups to modify the compound's properties. This compound's reactivity and structural characteristics make it particularly useful in the development of novel molecules with potential pharmacological activities.Furthermore, the presence of both bromine and chlorine atoms in 5-Bromo-8-chloroisoquinoline imparts an increased electron density and polarizability to the molecule, enhancing its interactions with other reagents in synthetic transformations. This reactivity profile makes it an attractive candidate for cross-coupling reactions, heterocyclic synthesis, and other advanced organic chemistry methodologies.Overall, the application of 5-Bromo-8-chloroisoquinoline in chemical synthesis enables chemists to access a diverse array of functionalized derivatives and complex molecular structures, paving the way for the exploration of new synthetic routes and the development of innovative compounds with potential therapeutic implications.
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