CymitQuimica logo

CAS 291536-42-0

:

5-(4-fluorobenzyl)-1,3-thiazolidine-2,4-dione

Description:
5-(4-Fluorobenzyl)-1,3-thiazolidine-2,4-dione is a chemical compound characterized by its thiazolidine ring structure, which incorporates a dione functional group. This compound features a 4-fluorobenzyl substituent, contributing to its unique properties and potential biological activity. The thiazolidine ring is known for its involvement in various pharmacological activities, including anti-inflammatory and antidiabetic effects. The presence of the fluorobenzyl group may enhance lipophilicity and influence the compound's interaction with biological targets. This compound is typically synthesized through multi-step organic reactions, and its characterization can be confirmed using techniques such as NMR spectroscopy, mass spectrometry, and infrared spectroscopy. As with many thiazolidine derivatives, it may exhibit interesting reactivity and can serve as a scaffold for further chemical modifications in drug development. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards associated with its use.
Formula:C10H8FNO2S
InChI:InChI=1/C10H8FNO2S/c11-7-3-1-6(2-4-7)5-8-9(13)12-10(14)15-8/h1-4,8H,5H2,(H,12,13,14)
SMILES:c1cc(ccc1CC1C(=NC(=O)S1)O)F
Synonyms:
  • 2,4-Thiazolidinedione, 5-[(4-fluorophenyl)methyl]-
  • 5-(4-Fluorobenzyl)-1,3-thiazolidine-2,4-dione
  • Rosiglitazone Impurity (5-(4-Fluorobenzyl)-2,4-thiazolidinedione)
  • Pioglitazone Impurity 12
  • 5-(4-Fluorobenzyl)-2,4-thiazolidinedione
  • 5-[(4-Fluorophenyl)methyl]-2,4-thiazolidinedione
  • 5-[(4-fluorophenyl)methyl]-1,3-thiazolidine-2,4-dione
  • Pioglitazone Fluoro IMpurity
  • Pioglitazone impurities1594
  • 5-(4-Fluorobenzyl)thiazolidine-2,4-dione
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 7 products.