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Home  > 6-Chloro-1h-pyrrolo[3,2-c]pyridine-3-carboxylic acid

AA00423

1000341-67-2 | 6-Chloro-1h-pyrrolo[3,2-c]pyridine-3-carboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $32.00 $23.00 -   +
250mg 97% in stock $33.00 $24.00 -   +
1g 97% in stock $111.00 $78.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA00423
Chemical Name: 6-Chloro-1h-pyrrolo[3,2-c]pyridine-3-carboxylic acid
CAS Number: 1000341-67-2
Molecular Formula: C8H5ClN2O2
Molecular Weight: 196.5905
MDL Number: MFCD09749984
SMILES: Clc1ncc2c(c1)[nH]cc2C(=O)O

 

Upstream Synthesis Route
  • 6-Chloro-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid, also known as $name$, is a valuable compound widely used in chemical synthesis. Due to its unique structure and functional groups, this compound serves as a versatile building block in organic chemistry. One of the key applications of $name$ is its use as a key intermediate in the synthesis of pharmaceutical compounds. The presence of the carboxylic acid group allows for derivatization, enabling the introduction of various functional groups to tailor the properties of the final molecule. This makes $name$ an essential starting material in the development of new drugs and biologically active molecules.Additionally, the presence of the pyrrolopyridine core in $name$ imparts interesting electronic and steric properties to the molecule. This structural motif is often utilized in the design of biologically active compounds, such as antimicrobial agents, anticancer drugs, and enzyme inhibitors. The ability to modify and functionalize the pyrrolopyridine core makes $name$ a valuable tool for medicinal chemists seeking to create novel bioactive molecules.Overall, the application of 6-Chloro-1H-pyrrolo[3,2-c]pyridine-3-carboxylic acid in chemical synthesis offers a wide range of possibilities for the development of diverse organic molecules with potential pharmaceutical and biological activities.
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