Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
17951
CAS Number:
132089-35-1
Ester éthylique de l'acide 2-(4-fluorophényl)thiazole-4-carboxylique
Purity:
≥ 95 % (HPLC)
Documents
$67.60 /100 mg
Taille
Request Bulk Quote
Product Information

2-(4-Fluorophenyl)thiazole-4-carboxylic acid ethyl ester is a versatile compound with significant applications in pharmaceuticals and agrochemicals. This compound features a unique thiazole ring that enhances its biological activity, making it a valuable building block in the synthesis of various medicinal agents. Its fluorophenyl group contributes to its lipophilicity, which can improve the compound's ability to penetrate biological membranes, thereby increasing its efficacy in drug formulations. Researchers have utilized this compound in the development of anti-inflammatory and antimicrobial agents, showcasing its potential in addressing various health challenges.

In addition to its pharmaceutical applications, 2-(4-Fluorophenyl)thiazole-4-carboxylic acid ethyl ester is also explored in the agrochemical sector for its potential as a pesticide or herbicide. Its unique chemical structure allows for targeted action against specific pests while minimizing environmental impact. This compound stands out due to its favorable safety profile and effectiveness, making it an attractive option for researchers and industry professionals looking to innovate in both health and agricultural fields.

CAS Number
132089-35-1
Purity
≥ 95 % (HPLC)
Molecular Formula
C 12 H 10 FNO 2 S
Molecular Weight
251.28
MDL Number
MFCD06738337
PubChem ID
15170574
Appearance
Solide jaune
Conditions
Conserver à 0-8°C
General Information
CAS Number
132089-35-1
Purity
≥ 95 % (HPLC)
Molecular Formula
C 12 H 10 FNO 2 S
Molecular Weight
251.28
MDL Number
MFCD06738337
PubChem ID
15170574
Appearance
Solide jaune
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

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

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic drugs. Its unique structure allows for targeted modifications that enhance therapeutic efficacy.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, including herbicides and fungicides, providing effective solutions for pest control while minimizing environmental impact.
  • Material Science: The compound is explored for its potential in developing advanced materials, such as polymers and coatings, that require specific thermal and mechanical properties.
  • Biochemical Research: Researchers utilize this compound to study enzyme interactions and metabolic pathways, aiding in the understanding of biological processes and disease mechanisms.
  • Analytical Chemistry: It is employed as a standard reference material in various analytical techniques, ensuring accuracy and reliability in chemical analysis and quality control processes.

Citations