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Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aromatic Heterocycles  > 5-(Trifluoromethyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxylic acid

AA17797

1171920-15-2 | 5-(Trifluoromethyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $43.00 $31.00 -   +
250mg 95% in stock $68.00 $48.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA17797
Chemical Name: 5-(Trifluoromethyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxylic acid
CAS Number: 1171920-15-2
Molecular Formula: C9H5F3N2O2
Molecular Weight: 230.1434
MDL Number: MFCD12922778
SMILES: OC(=O)c1c[nH]c2c1cc(cn2)C(F)(F)F

 

Computed Properties
Complexity: 295  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 1  
XLogP3: 1.7  

 

 

Upstream Synthesis Route
  • 5-(Trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid is a versatile compound widely used in chemical synthesis as a valuable building block. With its unique structural features, this compound plays a crucial role in the development of novel pharmaceuticals, agrochemicals, and materials.This compound serves as a key intermediate in the synthesis of various biologically active molecules due to its ability to participate in diverse chemical reactions. Its trifluoromethyl group enhances the compound's lipophilicity and metabolic stability, making it a desirable component in drug discovery and development processes.In organic transformations, 5-(Trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid serves as a precursor for the introduction of the trifluoromethyl functionality into target molecules, enabling medicinal chemists to modulate the properties of organic compounds for improved pharmacokinetic profiles.Furthermore, this compound's pyrrolopyridine core scaffold offers a rich chemical diversity, allowing for further derivatization to generate libraries of structurally diverse compounds. This versatility makes 5-(Trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid a valuable tool in the synthesis of complex molecules with potential applications in drug discovery and materials science.
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