5-(4-Bromophenyl)pyrimidine is an organic compound characterized by its pyrimidine ring, which is a six-membered heterocyclic structure containing two nitrogen atoms at positions 1 and 3. The compound features a bromophenyl substituent at the 5-position of the pyrimidine ring, which contributes to its chemical reactivity and potential applications in medicinal chemistry. The presence of the bromine atom enhances the compound's lipophilicity and can influence its biological activity. This compound is typically used in the synthesis of various pharmaceuticals and agrochemicals due to its ability to act as a building block in organic synthesis. It may exhibit interesting properties such as fluorescence or specific interactions with biological targets, making it a subject of research in drug development. Additionally, its molecular structure allows for potential modifications that can lead to derivatives with enhanced efficacy or selectivity in biological applications. Safety and handling precautions should be observed due to the presence of bromine, which can be hazardous.

5-(4-Bromophenyl)pyrimidine

160377-42-4: 5-(4-Bromophenyl)pyrimidine is an organic compound characterized by its pyrimidine ring, which is a six-membered heterocyclic structure containing two nitrogen atoms at positions 1 and 3. The compound features a bromophenyl substituent at the 5-position of the pyrimidine ring, which contributes to its chemical reactivity and potential applications in medicinal chemistry. The presence of the bromine atom enhances the compound's lipophilicity and can influence its biological activity. This compound is typically used in the synthesis of various pharmaceuticals and agrochemicals due to its ability to act as a building block in organic synthesis. It may exhibit interesting properties such as fluorescence or specific interactions with biological targets, making it a subject of research in drug development. Additionally, its molecular structure allows for potential modifications that can lead to derivatives with enhanced efficacy or selectivity in biological applications. Safety and handling precautions should be observed due to the presence of bromine, which can be hazardous.

CAS 160377-42-4

5-(4-Bromophenyl)pyrimidine

Pyrimidine, 5-(4-bromophenyl)-

Ref: IN-DA00HYLF

5-(4-Bromophenyl)pyrimidine

Ref: 54-OR1058513

5-(4-Bromophenyl)pyrimidine

Ref: 10-F516456