4-Amino-5-cyanopyrimidine is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. This compound features an amino group (-NH2) at the 4-position and a cyano group (-C≡N) at the 5-position of the pyrimidine ring, contributing to its reactivity and potential applications in various chemical syntheses. It is typically a crystalline solid that is soluble in polar solvents, reflecting its polar functional groups. The presence of both the amino and cyano groups makes it a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, 4-amino-5-cyanopyrimidine can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions, making it valuable in organic synthesis. Its properties, such as melting point and boiling point, can vary based on purity and environmental conditions. As with many nitrogen-containing heterocycles, it may exhibit biological activity, warranting further investigation in medicinal chemistry.

4-Amino-5-cyanopyrimidine

16357-69-0: 2-Amino-5-cyanopyrimidine, 4-Amino-5-Cyanopyrimidine, 4-Amino-5-Pyrimidinecarbonitrile, 4-Amino-pyrimidine-5-carbonitrile, 5-Pyrimidinecarbonitrile, 4-amino-, Buttpark 77\12-50, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 

CAS 16357-69-0: 4-Amino-5-cyanopyrimidine

4-Aminopyrimidine-5-carbonitrile

Ref: 10-F068724

5-Pyrimidinecarbonitrile, 4-amino-

Ref: IN-DA001U8O

4-Aminopyrimidine-5-carbonitrile

Ref: 3B-A1214

4-Aminopyrimidine-5-carbonitrile

Ref: 54-OR29186