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Catalog Number:
24937
CAS Number:
64837-53-2
5-amino-1,3,4-thiadiazole-2-carboxylate d'éthyle
Purity:
≥ 97 % (HPLC)
Synonym(s):
Ester éthylique de l'acide 5-amino-1,3,4-thiadiazole-2-carboxylique
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Product Information

Ethyl 5-amino-1,3,4-thiadiazole-2-carboxylate is a versatile compound known for its unique thiadiazole structure, which enhances its reactivity and potential applications in various fields. This compound serves as a valuable intermediate in the synthesis of pharmaceuticals, particularly in the development of antimicrobial agents and anti-inflammatory drugs. Its ability to act as a building block for more complex molecules makes it a preferred choice among researchers and industry professionals looking to innovate in drug design.

In addition to its pharmaceutical applications, Ethyl 5-amino-1,3,4-thiadiazole-2-carboxylate is also utilized in agricultural chemistry, where it contributes to the formulation of effective agrochemicals. Its properties allow for the development of compounds that can enhance crop protection and yield. With its favorable characteristics, this compound stands out as a crucial ingredient in both medicinal and agricultural formulations, providing significant benefits in efficiency and effectiveness.

Synonyms
Ester éthylique de l'acide 5-amino-1,3,4-thiadiazole-2-carboxylique
CAS Number
64837-53-2
Purity
≥ 97 % (HPLC)
Molecular Formula
C5H7N3O2S
Molecular Weight
173.2
MDL Number
MFCD03093787
PubChem ID
2756556
Melting Point
196-202 ?C
Appearance
Cristaux blancs
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Ester éthylique de l'acide 5-amino-1,3,4-thiadiazole-2-carboxylique
CAS Number
64837-53-2
Purity
≥ 97 % (HPLC)
Molecular Formula
C5H7N3O2S
Molecular Weight
173.2
MDL Number
MFCD03093787
PubChem ID
2756556
Melting Point
196-202 ?C
Appearance
Cristaux blancs
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 5-amino-1,3,4-thiadiazole-2-carboxylate is widely utilized in research focused on:

  • Agricultural Chemistry: This compound serves as a building block for developing new agrochemicals, particularly fungicides and herbicides, enhancing crop protection and yield.
  • Pharmaceutical Development: It is explored for its potential in synthesizing novel pharmaceuticals, especially in the treatment of infections and inflammatory diseases, due to its unique chemical structure.
  • Material Science: The compound is used in the formulation of specialty polymers and coatings, providing improved durability and resistance to environmental factors.
  • Analytical Chemistry: It acts as a reagent in various analytical methods, aiding in the detection and quantification of other chemical species in complex mixtures.
  • Biotechnology: Ethyl 5-amino-1,3,4-thiadiazole-2-carboxylate is investigated for its role in biocatalysis, potentially improving the efficiency of enzymatic reactions in industrial processes.

Citations