CAS 661463-79-2
:1,2,4-Triazine-3,5(2H,4H)-dione, 6-(2,3-dichlorophenyl)-
Description:
1,2,4-Triazine-3,5(2H,4H)-dione, 6-(2,3-dichlorophenyl)-, identified by CAS number 661463-79-2, is a heterocyclic organic compound characterized by its triazine ring structure, which contains three nitrogen atoms and two carbonyl groups. This compound features a dichlorophenyl substituent at the 6-position, contributing to its potential biological activity and chemical reactivity. The presence of chlorine atoms enhances its lipophilicity and may influence its interaction with biological targets. Typically, compounds of this class exhibit properties such as antimicrobial, antifungal, or herbicidal activities, making them of interest in agricultural and pharmaceutical applications. The molecular structure allows for various synthetic modifications, which can lead to derivatives with enhanced efficacy or selectivity. Additionally, the stability of the triazine ring under various conditions is a notable characteristic, making it suitable for diverse applications in chemical synthesis and material science. Overall, this compound exemplifies the complexity and utility of nitrogen-containing heterocycles in modern chemistry.
Formula:C9H5Cl2N3O2
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Found 5 products.
Lamotrigine EP Impurity D
CAS:Formula:C9H5Cl2N3O2Color and Shape:Off-White SolidMolecular weight:258.066-(2,3-Dichlorophenyl)-1,2,4-triazine-3,5(2H,4H)-dione
CAS:Controlled ProductFormula:C9H5Cl2N3O2Color and Shape:NeatMolecular weight:258.063,5-Didesamino-3,5-dioxo Lamotrigine
CAS:Controlled Product<p>Impurity Lamotrigine EP Impurity D<br>Applications 3,5-Didesamino-3,5-dioxo Lamotrigine (Lamotrigine EP Impurity D) is an impurity of the anticonvulsant Lamotrigine (L173250).<br>References Hlavac, J. et al.: ARKIVOC, 1, 22 (2003);<br></p>Formula:C9H5Cl2N3O2Color and Shape:NeatMolecular weight:258.066-(2,3-Dichlorophenyl)-1,2,4-triazine-3,5(2H,4H)-dione
CAS:6-(2,3-Dichlorophenyl)-1,2,4-triazine-3,5(2H,4H)-dione is a chlorinating agent that converts alcohols to alkyl chlorides. It is used for the conversion of diazotizable aromatic compounds to diazo compounds. This compound has been shown to be neuroprotective in animal models and provides protection against glutamate excitotoxicity. 6-(2,3-Dichlorophenyl)-1,2,4-triazine-3,5(2H,4H)-dione also reacts with nitrite ions to form the corresponding nitroso derivatives. These derivatives can cause DNA damage and are mutagenic. 6-(2,3-Dichlorophenyl)-1,2,4-triazine-3,5(2H,4H)-dione has been shown to react with aminoguanidine to produce a chromatFormula:C9H5Cl2N3O2Purity:Min. 95%Color and Shape:PowderMolecular weight:258.06 g/mol




