logo
Home  > Chemistry  > Organic Building Blocks  > Fluorinated Building Blocks  > 2-Cyclopropyl-4-(4-fluorophenyl)quinoline-3-carbaldehyde

AA53600

121660-37-5 | 2-Cyclopropyl-4-(4-fluorophenyl)quinoline-3-carbaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
200mg 95% in stock $14.00 $10.00 -   +
250mg 95% in stock $15.00 $11.00 -   +
1g 95% in stock $18.00 $13.00 -   +
5g 95% in stock $63.00 $45.00 -   +
10g 95% in stock $113.00 $79.00 -   +
25g 95% in stock $135.00 $95.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA53600
Chemical Name: 2-Cyclopropyl-4-(4-fluorophenyl)quinoline-3-carbaldehyde
CAS Number: 121660-37-5
Molecular Formula: C19H14FNO
Molecular Weight: 291.319
MDL Number: MFCD09032925
SMILES: O=Cc1c(nc2c(c1c1ccc(cc1)F)cccc2)C1CC1

 

Computed Properties
Complexity: 402  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 22  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 3  
XLogP3: 4  

 

 

Upstream Synthesis Route
  • 2-Cyclopropyl-4-(4-fluorophenyl)quinoline-3-carboxaldehyde is a versatile compound widely used in chemical synthesis. It serves as a key building block in the construction of various organic molecules due to its unique structure and reactivity. One of the main applications of 2-Cyclopropyl-4-(4-fluorophenyl)quinoline-3-carboxaldehyde is in the synthesis of heterocyclic compounds. By reacting with different reagents and functional groups, this compound can be employed in the preparation of novel pharmaceuticals, agrochemicals, and other biologically active molecules. Its cyclic structure and carbonyl functionality make it a valuable intermediate in the formation of complex organic frameworks.Additionally, 2-Cyclopropyl-4-(4-fluorophenyl)quinoline-3-carboxaldehyde can be utilized in ligand synthesis for coordination chemistry and catalysis. Its ability to coordinate with metal ions makes it a useful ligand in various metal-catalyzed reactions, enabling the design of new catalyst systems with enhanced reactivity and selectivity.Overall, the application of 2-Cyclopropyl-4-(4-fluorophenyl)quinoline-3-carboxaldehyde in chemical synthesis showcases its significance in driving innovation and advancement in the field of organic chemistry.
FEATURED PRODUCTS