CymitQuimica logo

CAS 129295-31-4

:

6-CHLORO-1H-INDAZOLE-3-CARBOXYLIC ACID

Description:
6-Chloro-1H-indazole-3-carboxylic acid is a chemical compound characterized by its indazole core, which is a bicyclic structure containing a five-membered ring fused to a six-membered ring. The presence of a chlorine atom at the 6-position and a carboxylic acid functional group at the 3-position contributes to its unique chemical properties. This compound is typically a white to off-white solid and is soluble in polar solvents, which is common for carboxylic acids. It may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of potential therapeutic agents. The compound's structure allows for various chemical modifications, which can enhance its efficacy or alter its pharmacokinetic properties. Additionally, its reactivity can be influenced by the electron-withdrawing nature of the chlorine atom, affecting its interactions in chemical reactions. As with many indazole derivatives, it may also participate in hydrogen bonding due to the presence of the carboxylic acid group, which can play a significant role in its biological activity and solubility.
Formula:C8H5ClN2O2
InChI:InChI=1/C8H5ClN2O2/c9-4-1-2-5-6(3-4)10-11-7(5)8(12)13/h1-3H,(H,10,11)(H,12,13)
InChI key:InChIKey=MCGHMISXTKQRRF-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C=2C(NN1)=CC(Cl)=CC2
Synonyms:
  • 1H-Indazole-3-carboxylic acid, 6-chloro-
  • 6-Chloro-3-(1H)Indazole Carboxylic Acid
  • 6-Chloroindazole-3-Carboxylic Acid
  • 6-Chloro-1H-indazole-3-carboxylic acid
  • 6-Chloro-1H-indazole-3-carboxylic acid 97%
  • 3-Carboxy-6-chloro-1H-indazole
  • 6-chloro-1H-indazol-3-carboxylic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.