CymitQuimica logo

CAS 885279-72-1

:

Methyl 4-(3-aminophenyl)-2-thiazolecarboxylate

Description:
Methyl 4-(3-aminophenyl)-2-thiazolecarboxylate is an organic compound characterized by its thiazole and aromatic amine functional groups. It features a thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen, contributing to its unique chemical properties. The presence of the methyl ester group enhances its solubility in organic solvents and may influence its reactivity. The compound's structure includes an amino group attached to a phenyl ring, which can participate in hydrogen bonding and may affect its biological activity. This compound is of interest in medicinal chemistry, potentially serving as a scaffold for the development of pharmaceuticals due to its ability to interact with biological targets. Its synthesis typically involves multi-step organic reactions, and it may exhibit various properties such as moderate to high stability under standard conditions. Additionally, its potential applications could extend to fields such as agrochemicals or materials science, depending on its specific interactions and reactivity profiles. Safety and handling precautions should be observed, as with any chemical substance.
Formula:C11H10N2O2S
InChI:InChI=1S/C11H10N2O2S/c1-15-11(14)10-13-9(6-16-10)7-3-2-4-8(12)5-7/h2-6H,12H2,1H3
InChI key:InChIKey=OAUXBAJKZQHHOH-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=NC(=CS1)C2=CC(N)=CC=C2
Synonyms:
  • 2-Thiazolecarboxylic acid, 4-(3-aminophenyl)-, methyl ester
  • 4-(3-Amino-Phenyl)-Thiazole-2-Carboxylic Acid Methyl Ester
  • Methyl 4-(3-aminophenyl)-2-thiazolecarboxylate
  • Methyl 4-(3-aMinophenyl)thiazole-2-carboxylate
  • 2-Thiazolecarboxylicacid, 4-(3-aminophenyl)-, methyl ester
  • methyl 4-(3-aminophenyl)-1,3-thiazole-2-carboxylate
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.