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CAS 32955-21-8

Ethyl 2-Aminothiazole-5-carboxylate TCI E0907

Ethyl 2-Aminothiazole-5-carboxylate TCI E0907

Chemical Identity

Other names
2-Aminothiazole-5-carboxylic Acid Ethyl Ester
CAS No.
32955-21-8
PubChem
CID 314628·SID 160871464
Formula
C6H8N2O2S
Molecular weight
172.20 g/mol
Purity
>97.0%(HPLC)(T)
Storage
0-10°C
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
ethyl 2-amino-1,3-thiazole-5-carboxylate
SMILES
CCOC(=O)C1=CN=C(S1)N
InChIKey
VNZXERIGKZNEKB-UHFFFAOYSA-N
MDL
MDL00602139
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Ethyl 2-Aminothiazole-5-carboxylate is a chemical compound widely used as a building block in the synthesis of heterocyclic compounds. It plays a crucial role in organic chemistry laboratories by serving as a versatile intermediate in the creation of complex molecular structures. This compound is particularly valued for its ability to participate in various chemical reactions, making it an essential tool for researchers working on the development of new pharmaceuticals and industrial chemicals. Its unique structure, combining a thiazole ring with an amino group, allows for a wide range of functional group modifications, enhancing its utility in synthetic pathways.

The compound's stability and controlled reactivity make it a preferred choice for laboratory applications. Its predictable behavior under different reaction conditions ensures reliable results, which is vital in research settings where precision is key. Additionally, Ethyl 2-Aminothiazole-5-carboxylate exhibits good solubility in common organic solvents, facilitating its use in a variety of synthetic protocols. These properties contribute to its popularity among chemists seeking a dependable and adaptable reagent for their experiments.

In Indonesian laboratories, Ethyl 2-Aminothiazole-5-carboxylate is commonly used in organic chemistry research, especially in the development of bioactive compounds. It is frequently employed in academic and industrial research settings to support the synthesis of new materials and drug candidates. Its availability and reliability make it a standard reagent in many chemical laboratories across Indonesia, supporting both educational and applied research initiatives.

  • Organic synthesis of bioactive compounds due to its versatile functional groups and reactivity.
  • Development of pharmaceutical intermediates because of its ability to undergo various chemical modifications.
  • Research in heterocyclic chemistry as a building block for complex molecular structures.
  • Industrial chemical production where stable and reactive compounds are required for process optimization.
  • Academic research in medicinal chemistry for the exploration of new drug candidates and molecular frameworks.

Brand TCI
CAS number 32955-21-8
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply formats
Physical form Solid powder
Storage Store in a cool, dry place away from direct sunlight and moisture

Ethyl 2-Aminothiazole-5-carboxylate should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a sealed container to prevent moisture absorption, which can affect its stability. Suitable storage containers include glass or high-density polyethylene bottles to ensure chemical compatibility. Avoid exposure to direct sunlight and heat sources to prevent degradation. In a laboratory setting, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. Regular monitoring of storage conditions is advised to maintain the quality and usability of the compound in research applications.

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