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Catalog Number:
25674
CAS Number:
64399-23-1
2-amino-4-phénylthiazole-5-carboxylate d'éthyle
Purity:
≥ 97 % (HPLC)
Synonym(s):
Ester éthylique de l'acide 2-amino-4-phénylthiazole-5-carboxylique
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Product Information

Ethyl 2-amino-4-phenylthiazole-5-carboxylate is a versatile compound recognized for its significant role in pharmaceutical and chemical research. This compound features a thiazole ring, which is known for its biological activity, making it a valuable building block in the synthesis of various bioactive molecules. Its unique structure allows for potential applications in drug development, particularly in the creation of novel therapeutic agents targeting a range of diseases. Researchers have utilized this compound in the synthesis of anti-inflammatory and antimicrobial agents, showcasing its importance in medicinal chemistry.

In addition to its pharmaceutical applications, Ethyl 2-amino-4-phenylthiazole-5-carboxylate can also serve as an intermediate in the production of agrochemicals and dyes, expanding its utility across different industries. Its favorable properties, such as stability and reactivity, make it an attractive option for researchers looking to innovate in their respective fields. With its broad applicability and potential for further development, this compound stands out as a key player in advancing both scientific research and industrial applications.

Synonyms
Ester éthylique de l'acide 2-amino-4-phénylthiazole-5-carboxylique
CAS Number
64399-23-1
Purity
≥ 97 % (HPLC)
Molecular Formula
C12H12N2O2S
Molecular Weight
248.31
MDL Number
MFCD00022452
PubChem ID
73239
Melting Point
167-175 ?C
Appearance
Cristaux jaune pâle
Conditions
Conserver à 0-8°C
General Information
Synonyms
Ester éthylique de l'acide 2-amino-4-phénylthiazole-5-carboxylique
CAS Number
64399-23-1
Purity
≥ 97 % (HPLC)
Molecular Formula
C12H12N2O2S
Molecular Weight
248.31
MDL Number
MFCD00022452
PubChem ID
73239
Melting Point
167-175 ?C
Appearance
Cristaux jaune pâle
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

Ethyl 2-amino-4-phenylthiazole-5-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its ability to cross the blood-brain barrier.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, providing effective solutions for pest control and enhancing crop yield by acting as a growth regulator.
  • Biochemical Research: Researchers leverage its properties to study enzyme inhibition and protein interactions, making it valuable in the development of novel biochemical assays.
  • Material Science: The compound is explored for its potential in creating advanced materials, including polymers and coatings, that require specific thermal and mechanical properties.
  • Analytical Chemistry: It is utilized as a reference standard in analytical methods, aiding in the accurate quantification of similar compounds in complex mixtures.

Citations