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Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aromatic Heterocycles  > 5-Fluoro-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde

AA17796

1171920-17-4 | 5-Fluoro-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $40.00 $28.00 -   +
250mg 97% in stock $95.00 $67.00 -   +
5g 97% in stock $1,092.00 $765.00 -   +
10g 97% in stock $1,879.00 $1,316.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA17796
Chemical Name: 5-Fluoro-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde
CAS Number: 1171920-17-4
Molecular Formula: C8H5FN2O
Molecular Weight: 164.1365
MDL Number: MFCD12922779
SMILES: Fc1cc2c(C=O)c[nH]c2nc1

 

Computed Properties
Complexity: 188  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 0.9  

 

 

Upstream Synthesis Route
  • 5-Fluoro-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde, also known as $name$, is a versatile building block commonly utilized in organic synthesis due to its unique chemical properties. This compound serves as a crucial intermediate in the preparation of various pharmaceuticals, agrochemicals, and functional materials.In chemical synthesis, $name$ is commonly employed as a key starting material for the construction of heterocyclic compounds with diverse biological activities. Its specific structural features make it an essential component in the development of new drug candidates and molecular probes. By participating in a variety of organic transformations, including N-alkylations, nucleophilic additions, and cyclization reactions, $name$ enables the efficient synthesis of complex molecules with high chemical diversity.Moreover, the presence of the fluoro substituent in $name$ enhances its reactivity and alters the electronic properties of the resulting compounds. This modification can lead to improved pharmacological profiles, such as enhanced bioavailability, target selectivity, and metabolic stability. As a result, $name$ plays a crucial role in the design and synthesis of novel chemical entities with potential applications in drug discovery and development.Overall, the strategic incorporation of 5-Fluoro-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde in chemical synthesis enables the rapid and efficient assembly of complex molecular architectures, making it a valuable tool for organic chemists engaged in the exploration of new chemical space and the creation of innovative materials.
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