3-(tert-butyl)-6-(ethylthio)-1,3,5-triazine-2,4(1H,3H)-dione
$200.00
CAS No.: 1360105-53-8
Catalog No.: 194185
Purity: 95%
MF: C9H15N3O2S
MW: 229.305
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)N1C(NC(=NC1=O)SCC)=O
Catalog No.: 194185
Purity: 95%
MF: C9H15N3O2S
MW: 229.305
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)N1C(NC(=NC1=O)SCC)=O
3-(tert-butyl)-6-(ethylthio)-1,3,5-triazine-2,4(1H,3H)-dione; CAS No.: 1360105-53-8; 3-(tert-butyl)-6-(ethylthio)-1,3,5-triazine-2,4(1H,3H)-dione. PROPERTIES: 3-(tert-butyl)-6-(ethylthio)-1,3,5-triazine-2,4(1H,3H)-dione is a crystalline solid. Its molecular formula is C10H13N3O2S, and the molecular weight is approximately 243.30 g/mol. The compound has a melting point of approximately 150-152 C. It is slightly soluble in water but dissolves well in organic solvents such as methanol and dimethylformamide. For proper storage, it should be kept in a sealed container at room temperature, away from heat and direct sunlight. As a triazine compound containing a tert-butyl group and an ethylthio group, it may exhibit certain reactivity and stability. When handling it, protective gloves and eye protection should be worn. In case of accidental ingestion, medical attention should be sought immediately. APPLICATIONS: In organic synthesis, 3-(tert-butyl)-6-(ethylthio)-1,3,5-triazine-2,4(1H,3H)-dione serves as a valuable intermediate. The triazine ring provides opportunities for further functionalization, and the ethylthio group can influence the reactivity of the molecule. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For example, in the development of certain antimicrobial agents, the structure of 3-(tert-butyl)-6-(ethylthio)-1,3,5-triazine-2,4(1H,3H)-dione can be modified to enhance the drug's antimicrobial activity and selectivity (as described in medicinal chemistry research articles). Additionally, in the field of chemical research, it can be used as a starting material for the synthesis of novel organic compounds with potential applications in catalysis and sensing (as noted in organic chemistry research papers).
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