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Catalog Number:
44041
CAS Number:
53266-94-7
Ethyl (2-amino-4-thiazolyl)acetate
Purity:
≥ 98% (GC)
Synonym(s):
(2-Amino-4-thiazolyl)acetic acid ethyl ester
Documents
$40.66 /25G
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Product Information

Ethyl (2-amino-4-thiazolyl)acetate is a versatile compound recognized for its significant role in pharmaceutical and agricultural applications. This compound, also known as ethyl 2-(2-amino-1,3-thiazol-4-yl)acetate, features a thiazole ring that enhances its biological activity, making it a valuable intermediate in the synthesis of various bioactive molecules. Researchers utilize this compound in the development of pharmaceuticals, particularly in the creation of antimicrobial and anti-inflammatory agents, due to its ability to interact effectively with biological targets.

In addition to its pharmaceutical relevance, Ethyl (2-amino-4-thiazolyl)acetate is also employed in agricultural chemistry, where it serves as a building block for agrochemicals aimed at improving crop protection and yield. Its unique thiazole structure provides a pathway for the design of novel pesticides and herbicides, offering potential advantages over traditional compounds in terms of efficacy and environmental safety. This compound's diverse applications make it an essential choice for researchers and industry professionals looking to innovate in their respective fields.

Synonyms
(2-Amino-4-thiazolyl)acetic acid ethyl ester
CAS Number
53266-94-7
Purity
≥ 98% (GC)
Molecular Formula
C7H10N2O2S
Molecular Weight
186.23
MDL Number
MFCD00005330
PubChem ID
104454
Melting Point
92 - 96 °C
Appearance
Light yellow to brown crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
(2-Amino-4-thiazolyl)acetic acid ethyl ester
CAS Number
53266-94-7
Purity
≥ 98% (GC)
Molecular Formula
C7H10N2O2S
Molecular Weight
186.23
MDL Number
MFCD00005330
PubChem ID
104454
Melting Point
92 - 96 °C
Appearance
Light yellow to brown crystalline powder
Conditions
Store at 2 - 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 (2-amino-4-thiazolyl)acetate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly those targeting infectious diseases and cancer. Its thiazole ring structure enhances biological activity, making it a valuable component in drug formulation.
  • Agricultural Chemicals: It is used in the development of agrochemicals, including fungicides and herbicides. The compound's effectiveness in inhibiting specific plant pathogens can lead to improved crop yields and healthier plants.
  • Biochemical Research: Researchers utilize this compound in studies related to enzyme inhibition and protein interactions. Its unique structure allows for the exploration of new biochemical pathways and therapeutic targets.
  • Material Science: Ethyl (2-amino-4-thiazolyl)acetate is also explored in the creation of novel materials, such as polymers and coatings, which can exhibit enhanced properties like durability and resistance to environmental factors.
  • Diagnostics: The compound is investigated for its potential use in diagnostic assays, particularly in detecting specific biomarkers associated with diseases. Its ability to bind selectively to certain biological targets can improve the accuracy of diagnostic tests.

Citations