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

AI10108

1160247-71-1 | tert-Butyl 2'-oxo-2',4'-dihydro-1'h-spiro[pyrrolidine-3,3'-quinoline]-1-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
25mg 95% in stock $322.00 $225.00 -   +
100mg 95% in stock $889.00 $622.00 -   +
250mg 95% in stock $1,463.00 $1,024.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AI10108
Chemical Name: tert-Butyl 2'-oxo-2',4'-dihydro-1'h-spiro[pyrrolidine-3,3'-quinoline]-1-carboxylate
CAS Number: 1160247-71-1
Molecular Formula: C17H22N2O3
Molecular Weight: 302.36818000000005
MDL Number: MFCD12198632
SMILES: O=C(N1CCC2(C1)Cc1ccccc1NC2=O)OC(C)(C)C

 

Computed Properties
Complexity: 471  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 22  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 1  
XLogP3: 1.9  

 

 

Upstream Synthesis Route
  • Tert-Butyl 2-Oxo-2,4-Dihydro-1H-Spiro[Pyrrolidine-3,3-Quinoline]-1-Carboxylate is a versatile compound widely utilized in chemical synthesis due to its unique structure and reactivity. In synthetic chemistry, this compound serves as a valuable building block for the construction of complex molecules with diverse functionalities. Its spirocyclic structure imparts rigidity and stereochemical control to synthetic pathways, making it a valuable intermediate in the preparation of biologically active compounds and natural product derivatives. Its ester functionality allows for facile manipulation through various chemical transformations, enabling the introduction of different substituents and functional groups to tailor the properties of the final product. Additionally, the presence of the carbonyl group offers opportunities for further derivatization, expanding the synthetic utility of this compound in the creation of novel molecular architectures.
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