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Home  > Chemistry  > Heterocyclic Building Blocks  > Tetrahydroquinolines  > tert-Butyl 2'-oxo-2',3'-dihydro-1'H-spiro[piperidine-4,4'-quinoline]-1-carboxylate

AE28113

1032143-13-7 | tert-Butyl 2'-oxo-2',3'-dihydro-1'H-spiro[piperidine-4,4'-quinoline]-1-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $341.00 $239.00 -   +
250mg 95% in stock $605.00 $423.00 -   +
1g 95% in stock $1,505.00 $1,054.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE28113
Chemical Name: tert-Butyl 2'-oxo-2',3'-dihydro-1'H-spiro[piperidine-4,4'-quinoline]-1-carboxylate
CAS Number: 1032143-13-7
Molecular Formula: C18H24N2O3
Molecular Weight: 316.3948
MDL Number: MFCD15530225
SMILES: O=C1Nc2ccccc2C2(C1)CCN(CC2)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 475  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 23  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 2.2  

 

 

Upstream Synthesis Route
  • The tert-Butyl 2'-oxo-2',3'-dihydro-1'H-spiro[piperidine-4,4'-quinoline]-1-carboxylate plays a crucial role in chemical synthesis due to its unique structure and reactivity. This compound is widely utilized as a versatile building block in the creation of complex organic molecules and pharmaceuticals. With its spirocyclic nature and functional groups, it enables the construction of diverse molecular scaffolds that are challenging to access using traditional synthetic methods. In addition, the presence of the tert-butyl ester group provides stability during various chemical transformations, allowing for selective modifications at specific positions. Researchers and chemists rely on tert-Butyl 2'-oxo-2',3'-dihydro-1'H-spiro[piperidine-4,4'-quinoline]-1-carboxylate as a valuable tool in the synthesis of novel compounds with potential applications in drug discovery, material science, and other areas of chemical research.
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