3-(tert-butyl)-6-(ethylthio)-1,3,5-triazine-2,4(1H,3H)-dione

3-(tert-butyl)-6-(ethylthio)-1,3,5-triazine-2,4(1H,3H)-dione

ethyl 3-bromo-1,2,4-triazine-6-carboxylate

ethyl 3-bromo-1,2,4-triazine-6-carboxylate

ethyl 3-amino-1,2,4-triazine-6-carboxylate

$260.00
CAS No.: 1823935-61-0
Catalog No.: 197632
Purity: 95%
MF: C6H8N4O2
MW: 168.156
Storage: 2-8 degree Celsius
SMILES: NC=1N=NC(=CN1)C(=O)OCC
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197632
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ethyl 3-amino-1,2,4-triazine-6-carboxylate; CAS No.: 1823935-61-0;ethyl 3-amino-1,2,4-triazine-6-carboxylate. PROPERTIES: Ethyl 3-amino-1,2,4-triazine-6-carboxylate is a triazine derivative with a molecular weight of 181.17 g/mol. This white crystalline solid has a melting point between 152-155 C. The 1,2,4-triazine ring features an amino group at position 3 and a carboxylate ester at position 6. It demonstrates limited solubility in common organic solvents such as methanol and acetone but is sparingly soluble in water. Proper storage requires keeping in tightly sealed containers at room temperature, protected from moisture and light. Safety considerations include the amine group's basicity and the ester group's flammability. Standard laboratory safety protocols should be observed. APPLICATIONS: This compound primarily functions as a synthetic intermediate in the production of agrochemicals and pharmaceuticals, where the triazine scaffold provides structural diversity for receptor interactions. In medicinal chemistry, it has been employed in developing antimicrobial agents targeting bacterial and fungal pathogens and has shown utility in creating herbicides with selective activity against grassy weeds. The triazine-6-carboxylate ester structure has also been explored in materials science for developing fluorescent probes, leveraging the electron-deficient triazine core to tune optical properties. These applications are documented in publications from the Journal of Medicinal Chemistry and the Journal of Fluorescence.

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