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Home  > 8-Bromo-4-chloro-6-methylquinoline-3-carboxylic acid ethyl ester

AE24262

1016828-40-2 | 8-Bromo-4-chloro-6-methylquinoline-3-carboxylic acid ethyl ester

Packsize Purity Availability Price Discounted Price    Quantity
250mg 2 weeks $696.00 $487.00 -   +
1g 2 weeks $1,233.00 $863.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE24262
Chemical Name: 8-Bromo-4-chloro-6-methylquinoline-3-carboxylic acid ethyl ester
CAS Number: 1016828-40-2
Molecular Formula: C13H11BrClNO2
Molecular Weight: 328.5889
MDL Number: MFCD09946074
SMILES: CCOC(=O)c1cnc2c(c1Cl)cc(cc2Br)C

 

Computed Properties
Complexity: 315  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 3  
XLogP3: 4.1  

 

 

Upstream Synthesis Route
  • 8-Bromo-4-chloro-6-methylquinoline-3-carboxylic acid ethyl ester, also known as $name$, is a versatile compound that finds extensive utility in chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals due to its unique structural properties and reactivity.In chemical synthesis, $name$ can be utilized as a key intermediate for the preparation of diverse derivatives through functional group transformations. Its bromo and chloro substituents offer opportunities for selective cross-coupling reactions, enabling the introduction of additional functional groups at specific positions on the quinoline ring. This flexibility allows chemists to tailor the molecular structure of the final product to achieve desired properties and biological activities.Moreover, the ethyl ester moiety in $name$ can serve as a protecting group or a handle for further modifications, facilitating the construction of more complex molecules. By carefully manipulating the ethyl ester functionality, chemists can control the timing and regioselectivity of subsequent chemical reactions, leading to efficient synthetic routes and high product yields.Overall, the strategic incorporation of 8-Bromo-4-chloro-6-methylquinoline-3-carboxylic acid ethyl ester in chemical synthesis endeavors enables the efficient and precise construction of diverse molecular entities with potential applications across various industries.
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