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Home  > 1H-Indole-3-carboxylic acid, octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester, stereoisomer

AA22117

115956-12-2 | 1H-Indole-3-carboxylic acid, octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester, stereoisomer

Packsize Purity Availability Price Discounted Price    Quantity
1mg 98% in stock $20.00 $14.00 -   +
5mg 98% in stock $36.00 $25.00 -   +
10mg 98% in stock $49.00 $34.00 -   +
100mg 98% in stock $218.00 $152.00 -   +
250mg 98% in stock $366.00 $256.00 -   +
1g 98% in stock $988.00 $691.00 -   +

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Description
Catalog Number: AA22117
Chemical Name: 1H-Indole-3-carboxylic acid, octahydro-3-oxo-2,6-methano-2H-quinolizin-8-yl ester, stereoisomer
CAS Number: 115956-12-2
Molecular Formula: C19H20N2O3
Molecular Weight: 324.3737
MDL Number: MFCD00865542
SMILES: O=C1CN2[C@H]3C[C@H]1C[C@@H]2C[C@H](C3)OC(=O)c1c[nH]c2c1cccc2

 

Computed Properties
Complexity: 535  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 2  
Heavy Atom Count: 24  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
XLogP3: 3.4  

 

 

Upstream Synthesis Route 
  • Dolasetron is a potent chemical compound that finds versatile applications in chemical synthesis processes. Primarily used as an antiemetic medication to treat nausea and vomiting resulting from chemotherapy or surgery, Dolasetron's unique properties also make it a valuable tool in the field of organic chemistry.In chemical synthesis, Dolasetron serves as a crucial intermediate in the production of various pharmaceutical compounds. Its stable structure and reactive functional groups allow for efficient derivatization and transformation into a wide range of desired molecules. Chemists often utilize Dolasetron as a building block to introduce specific chemical moieties or create complex structures that are challenging to access through traditional methods.Furthermore, Dolasetron's high purity and consistent reactivity make it a preferred choice for chemists working on the synthesis of bioactive compounds, such as drug candidates and pharmaceuticals. Its controlled and predictable reactivity enables chemists to design and execute precise synthetic pathways, ensuring the successful and efficient production of target molecules.Overall, Dolasetron's role in chemical synthesis underscores its significance beyond its primary pharmaceutical application, showcasing its potential as a valuable tool for advancing research and development in the field of organic chemistry.
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