2,2’-Bipyrimidine is an organic compound with the formula (C4H3N2)2. It is a derivative of the heterocycle pyrimidine and is a white solid . The compound is used as a bridging ligand in coordination chemistry .
A high-yield synthesis was developed for the preparation of 2,2’-bipyrimidine using the Ullmann coupling of 2-iodopyrimidine . The new procedure was also used for the preparation of 4,4’,6,6’-tetramethyl-2,2’-bipyrimidine and 5,5’-dibromo-2,2’-bipyrimidine . The present review describes the homogenous catalytic methodologies for the synthesis of 2,2’-bipyridines involving C−C bond formation from C−H bond .
The 2,2’-bipyrimidine crystal belongs to the monoclinic system, space group P2,/n, with two molecules per unit cell each on a Ci site group .
2,2’-Bipyrimidines have been shown to undergo multielectron reduction at low potentials . The major decomposition pathway was ultimately determined to be protonation of the dianion by solvent, which could be reversed by electrochemical or chemical oxidation .
2,2’-Bipyrimidine is an organic compound with the formula C8H6N4. Its molecular weight is 158.16 g/mol . It is a white solid .
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