Pyrimidine, 2,4,5-trifluoro- is a fluorinated derivative of pyrimidine, a six-membered heterocyclic compound containing two nitrogen atoms at positions 1 and 3. This specific compound features three fluorine atoms substituted at the 2, 4, and 5 positions of the pyrimidine ring, which significantly influences its chemical properties. The presence of fluorine atoms enhances the compound's electronegativity and lipophilicity, making it potentially useful in various applications, including pharmaceuticals and agrochemicals. Pyrimidine derivatives are known for their biological activity, and the trifluoromethyl groups can enhance the potency and selectivity of these compounds in biological systems. The compound is typically a colorless liquid or solid at room temperature, with a relatively low boiling point compared to non-fluorinated pyrimidines. It is important to handle this substance with care due to the potential toxicity associated with fluorinated compounds. As with many pyrimidine derivatives, it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it a versatile building block in organic synthesis.

Pyrimidine, 2,4,5-trifluoro-

17573-79-4: Pyrimidine, 2,4,5-trifluoro- is a fluorinated derivative of pyrimidine, a six-membered heterocyclic compound containing two nitrogen atoms at positions 1 and 3. This specific compound features three fluorine atoms substituted at the 2, 4, and 5 positions of the pyrimidine ring, which significantly influences its chemical properties. The presence of fluorine atoms enhances the compound's electronegativity and lipophilicity, making it potentially useful in various applications, including pharmaceuticals and agrochemicals. Pyrimidine derivatives are known for their biological activity, and the trifluoromethyl groups can enhance the potency and selectivity of these compounds in biological systems. The compound is typically a colorless liquid or solid at room temperature, with a relatively low boiling point compared to non-fluorinated pyrimidines. It is important to handle this substance with care due to the potential toxicity associated with fluorinated compounds. As with many pyrimidine derivatives, it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it a versatile building block in organic synthesis.

CAS 17573-79-4

Pyrimidine, 2,4,5-trifluoro-

Pyrimidine, 2,4,5-trifluoro-

Ref: IN-DA00215H

2,4,5-Trifluoropyrimidine

Ref: 54-PC5990

2,4,5-Trifluoropyrimidine

Ref: 10-F043808