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Catalog Number:
24936
CAS Number:
4970-53-0
Ethyl 5-amino-1,3,4-oxadiazole-2-carboxylate
Purity:
≥ 98% (HPLC)
Synonym(s):
5-Amino-1,3,4-oxadiazole-2-carboxylic acid ethyl ester
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Product Information

Ethyl 5-amino-1,3,4-oxadiazole-2-carboxylate is a versatile compound widely recognized for its applications in pharmaceuticals and agrochemicals. This compound features a unique oxadiazole ring structure, which enhances its biological activity and makes it an essential building block in the synthesis of various bioactive molecules. Researchers have utilized Ethyl 5-amino-1,3,4-oxadiazole-2-carboxylate in the development of novel drugs, particularly in the fields of anti-inflammatory and antimicrobial agents, due to its ability to modulate biological pathways effectively.

In addition to its pharmaceutical relevance, this compound is also valuable in agricultural chemistry, where it serves as a precursor for the synthesis of herbicides and fungicides. Its favorable properties, such as solubility and stability, make it an attractive option for formulation in various applications. With its broad spectrum of potential uses, Ethyl 5-amino-1,3,4-oxadiazole-2-carboxylate stands out as a key compound for researchers and industry professionals looking to innovate in drug development and crop protection.

Synonyms
5-Amino-1,3,4-oxadiazole-2-carboxylic acid ethyl ester
CAS Number
4970-53-0
Purity
≥ 98% (HPLC)
Molecular Formula
C5H7N3O3
Molecular Weight
157.13
MDL Number
MFCD03425200
PubChem ID
2756523
Melting Point
199-206 ?C
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
5-Amino-1,3,4-oxadiazole-2-carboxylic acid ethyl ester
CAS Number
4970-53-0
Purity
≥ 98% (HPLC)
Molecular Formula
C5H7N3O3
Molecular Weight
157.13
MDL Number
MFCD03425200
PubChem ID
2756523
Melting Point
199-206 ?C
Appearance
White 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

Ethyl 5-amino-1,3,4-oxadiazole-2-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, offering potential therapeutic benefits.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, contributing to the development of effective pesticides and herbicides that enhance crop yield and protect against pests.
  • Biochemical Research: Researchers employ this compound in studies related to enzyme inhibition and metabolic pathways, aiding in the understanding of biological processes and disease mechanisms.
  • Material Science: This chemical is explored for its potential applications in creating novel materials, such as polymers and coatings, that exhibit improved durability and resistance to environmental factors.
  • Analytical Chemistry: It is utilized as a reagent in various analytical methods, helping to detect and quantify other chemical substances, which is crucial in quality control and environmental monitoring.

Citations