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Home  > 4-Quinolinecarboxamide, 3-methyl-2-phenyl-N-[(1S)-1-phenylpropyl]-

AA92906

174635-69-9 | 4-Quinolinecarboxamide, 3-methyl-2-phenyl-N-[(1S)-1-phenylpropyl]-

Packsize Purity Availability Price Discounted Price    Quantity
1mg 95% in stock $28.00 $19.00 -   +
5mg 95% in stock $76.00 $53.00 -   +
10mg 95% in stock $115.00 $80.00 -   +
100mg 95% in stock $952.00 $666.00 -   +

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*All prices are in USD.

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Description
Catalog Number: AA92906
Chemical Name: 4-Quinolinecarboxamide, 3-methyl-2-phenyl-N-[(1S)-1-phenylpropyl]-
CAS Number: 174635-69-9
Molecular Formula: C26H24N2O
Molecular Weight: 380.4816
MDL Number: MFCD00944072
SMILES: CC[C@@H](c1ccccc1)NC(=O)c1c(C)c(nc2c1cccc2)c1ccccc1

 

Computed Properties
Complexity: 523  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 29  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 5  
XLogP3: 5.9  

 

 

Upstream Synthesis Route 
  • The product $name$ is a versatile compound known for its unique properties in chemical synthesis. One of its key applications is in the field of organic chemistry, where it serves as a valuable building block for the creation of complex molecules. Specifically, 3-methyl-2-phenyl-N-[(1S)-1-phenylpropyl]quinoline-4-carboxamide is utilized as a crucial intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals.This compound exhibits remarkable reactivity and selectivity in reactions such as acylation, alkylation, and cyclization, making it an indispensable tool for chemists seeking to construct intricate molecular structures. Its presence in a reaction mixture can facilitate the formation of new carbon-carbon and carbon-nitrogen bonds, enabling the synthesis of diverse organic compounds with enhanced biological or chemical activity.Furthermore, the unique structural features of 3-methyl-2-phenyl-N-[(1S)-1-phenylpropyl]quinoline-4-carboxamide make it a valuable substrate for transition metal-catalyzed transformations, including cross-coupling reactions and asymmetric catalysis. By harnessing the synthetic potential of this compound, researchers can access a wide range of structurally complex molecules that hold promise for applications in drug discovery, materials science, and beyond.
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