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Catalog Number:
06280
CAS Number:
19771-63-2
L-Thiazolidin-2-one-4-carboxylic acid
Purity:
≥ 95% (NMR)
Synonym(s):
L-2-Oxothiazolidine-4-carboxylic acid, (R-2-Oxothiazolidine-4-carboxylic acid
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Product Information

L-Thiazolidin-2-one-4-carboxylic acid is a versatile compound recognized for its unique thiazolidine structure, which contributes to its diverse applications in pharmaceuticals and biochemistry. This compound serves as a crucial building block in the synthesis of various bioactive molecules, particularly in the development of anti-inflammatory and antimicrobial agents. Its ability to form stable complexes with metal ions enhances its utility in catalysis and as a chelating agent, making it valuable in both research and industrial settings. Researchers have utilized L-Thiazolidin-2-one-4-carboxylic acid in the design of novel therapeutic agents, showcasing its potential in drug discovery and development.

In addition to its pharmaceutical applications, this compound is also explored for its role in agricultural chemistry, where it may contribute to the formulation of plant growth regulators. Its unique properties allow for targeted applications, providing an edge over similar compounds in terms of efficacy and specificity. With its promising applications and benefits, L-Thiazolidin-2-one-4-carboxylic acid stands out as a compound of interest for professionals seeking innovative solutions in their respective fields.

Synonyms
L-2-Oxothiazolidine-4-carboxylic acid, (R-2-Oxothiazolidine-4-carboxylic acid
CAS Number
19771-63-2
Purity
≥ 95% (NMR)
Molecular Formula
C4H5NO3S
Molecular Weight
147.15
MDL Number
MFCD00066092
PubChem ID
65272
Appearance
White crystalline powder
Conditions
Store at 0-8 °C
General Information
Synonyms
L-2-Oxothiazolidine-4-carboxylic acid, (R-2-Oxothiazolidine-4-carboxylic acid
CAS Number
19771-63-2
Purity
≥ 95% (NMR)
Molecular Formula
C4H5NO3S
Molecular Weight
147.15
MDL Number
MFCD00066092
PubChem ID
65272
Appearance
White crystalline powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

L-Thiazolidin-2-one-4-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of various pharmaceuticals, particularly those targeting metabolic disorders, due to its unique thiazolidine structure that enhances bioactivity.
  • Antioxidant Applications: It exhibits antioxidant properties, making it valuable in formulations aimed at reducing oxidative stress in biological systems, which is crucial in fields like nutrition and cosmetics.
  • Biochemical Research: Researchers use it to study enzyme interactions and metabolic pathways, providing insights into cellular processes and potential therapeutic targets.
  • Agricultural Chemistry: The compound is explored for its potential use in developing agrochemicals that promote plant growth and resistance to stress, contributing to sustainable agriculture practices.
  • Material Science: Its unique chemical properties allow for incorporation into polymers and materials, enhancing their performance in applications such as drug delivery systems and biodegradable plastics.

Citations