AA53600
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.
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 |
Complexity: | 402 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 22 |
Hydrogen Bond Acceptor Count: | 3 |
Rotatable Bond Count: | 3 |
XLogP3: | 4 |
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.