logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aromatic Heterocycles  > Ethyl 7-oxo-4,5,6,7-tetrahydro-1h-indole-2-carboxylate

AI12503

119647-73-3 | Ethyl 7-oxo-4,5,6,7-tetrahydro-1h-indole-2-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $48.00 $34.00 -   +
250mg 98% in stock $80.00 $56.00 -   +
500mg 98% in stock $144.00 $101.00 -   +
1g 98% in stock $225.00 $158.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AI12503
Chemical Name: Ethyl 7-oxo-4,5,6,7-tetrahydro-1h-indole-2-carboxylate
CAS Number: 119647-73-3
Molecular Formula: C11H13NO3
Molecular Weight: 207.22582000000008
MDL Number: MFCD03865893
SMILES: CCOC(=O)c1cc2c([nH]1)C(=O)CCC2

 

Computed Properties
Complexity: 277  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
XLogP3: 1.7  

 

 

Upstream Synthesis Route
  • In chemical synthesis, Ethyl 7-oxo-4,5,6,7-tetrahydro-1H-indole-2-carboxylate serves as a key intermediate compound with versatile applications. This compound plays a crucial role in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and functional groups allow for selective modifications and transformations, making it a valuable building block in organic synthesis.One common application of Ethyl 7-oxo-4,5,6,7-tetrahydro-1H-indole-2-carboxylate is in the synthesis of indole-based compounds, which are widely present in biologically active molecules such as drugs and natural products. By utilizing this compound as a starting material, chemists can efficiently access a wide range of structurally diverse compounds through different synthetic routes. Additionally, the presence of the ester group in Ethyl 7-oxo-4,5,6,7-tetrahydro-1H-indole-2-carboxylate enables further functionalization to introduce specific properties or enhance the biological activity of the final products.Moreover, Ethyl 7-oxo-4,5,6,7-tetrahydro-1H-indole-2-carboxylate can participate in various key reactions such as condensation, cyclization, and hydrogenation, making it a versatile and valuable intermediate in the development of new chemical entities. Its role in chemical synthesis extends to the creation of novel compounds for pharmaceutical research, agrochemical design, and material science applications. The strategic incorporation of this compound into synthetic pathways showcases its significance as a pivotal building block in the synthesis of complex molecules with diverse functionalities and applications in the field of chemistry.
FEATURED PRODUCTS