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Catalog Number:
17622
CAS Number:
61786-00-3
Ester éthylique de l'acide 2-(4-chlorophényl)thiazole-4-carboxylique
Purity:
≥ 99 % (HPLC)
Synonym(s):
2-(4-chlorophényl)-1,3-thiazole-4-carboxylate d'éthyle
Documents
$52.88 /250 mg
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Product Information

2-(4-Chlorophenyl)thiazole-4-carboxylic acid ethyl ester is a versatile compound known for its significant applications in pharmaceuticals and agrochemicals. This compound features a thiazole ring, which contributes to its biological activity, making it a valuable intermediate in the synthesis of various bioactive molecules. Its unique structure allows for the development of compounds with potential anti-inflammatory, antimicrobial, and antifungal properties, which are essential in drug discovery and development. Researchers often utilize this compound in the formulation of crop protection agents, enhancing agricultural productivity while ensuring environmental safety.

Additionally, the ethyl ester form of this compound provides improved solubility and bioavailability, making it an attractive option for formulation scientists. Its ability to act as a building block in the synthesis of more complex molecules opens up avenues for innovation in medicinal chemistry. With its favorable properties and practical applications, 2-(4-Chlorophenyl)thiazole-4-carboxylic acid ethyl ester stands out as a key player in advancing both pharmaceutical and agricultural research.

Synonyms
2-(4-chlorophényl)-1,3-thiazole-4-carboxylate d'éthyle
CAS Number
61786-00-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H10ClNO2S
Molecular Weight
267.74
MDL Number
MFCD00142031
PubChem ID
2799493
Appearance
Blanc cassé uni
Conditions
Conserver à 0-8°C
General Information
Synonyms
2-(4-chlorophényl)-1,3-thiazole-4-carboxylate d'éthyle
CAS Number
61786-00-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H10ClNO2S
Molecular Weight
267.74
MDL Number
MFCD00142031
PubChem ID
2799493
Appearance
Blanc cassé uni
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-(4-Chlorophenyl)thiazole-4-carboxylic acid ethyl ester is widely utilized in research focused on:

  • Agricultural Chemistry: This compound serves as a key ingredient in developing fungicides and pesticides, helping to protect crops from various diseases while promoting sustainable farming practices.
  • Pharmaceutical Development: It is explored for its potential in creating new therapeutic agents, particularly in treating bacterial infections and other diseases, due to its unique chemical structure.
  • Material Science: The compound is used in synthesizing advanced materials, such as polymers and coatings, which exhibit enhanced durability and resistance to environmental factors.
  • Analytical Chemistry: It plays a role in developing analytical methods for detecting and quantifying chlorinated compounds in environmental samples, aiding in pollution monitoring.
  • Biotechnology: Researchers utilize this compound in various biotechnological applications, including the development of biosensors that can detect specific biological markers.

Citations