5-Nitro-6-(trifluoromethyl)pyrimidine-2,4(1H,3H)-dione, with the CAS number 652-43-7, is a heterocyclic organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms. This compound features a nitro group (-NO2) at the 5-position and a trifluoromethyl group (-CF3) at the 6-position, contributing to its unique chemical properties. The presence of the dione functional groups (two carbonyls) at the 2 and 4 positions enhances its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and condensation reactions. The trifluoromethyl group imparts significant lipophilicity and can influence the compound's biological activity, often enhancing its potency in pharmaceutical applications. Additionally, the nitro group can participate in reduction reactions, further diversifying its chemical behavior. Overall, this compound is of interest in medicinal chemistry and agrochemicals due to its potential applications in drug development and as a building block in synthetic organic chemistry.

5-nitro-6-(trifluoromethyl)pyrimidine-2,4(1H,3H)-dione

652-43-7: 5-Nitro-6-(trifluoromethyl)pyrimidine-2,4(1H,3H)-dione, with the CAS number 652-43-7, is a heterocyclic organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms. This compound features a nitro group (-NO2) at the 5-position and a trifluoromethyl group (-CF3) at the 6-position, contributing to its unique chemical properties. The presence of the dione functional groups (two carbonyls) at the 2 and 4 positions enhances its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and condensation reactions. The trifluoromethyl group imparts significant lipophilicity and can influence the compound's biological activity, often enhancing its potency in pharmaceutical applications. Additionally, the nitro group can participate in reduction reactions, further diversifying its chemical behavior. Overall, this compound is of interest in medicinal chemistry and agrochemicals due to its potential applications in drug development and as a building block in synthetic organic chemistry.

CAS 652-43-7

5-nitro-6-(trifluoromethyl)pyrimidine-2,4(1H,3H)-dione

5-Nitro-6-(trifluoromethyl)-1,2,3,4-tetrahydropyrimidine-2,4-dione

Ref: 3D-AAA65243