16879-62-2

Usage

Chemical Family

bipyrimidine
2,6,2',6'-tetramethyl-[4,4']bipyrimidinyl is a part of the bipyrimidine family of compounds.

Derivative

bipyrimidine with methyl groups
It is a derivative of bipyrimidine with four methyl groups attached to the 2 and 6 positions of the molecule.

Usage

coordination chemistry and catalysis
The compound is commonly used as a ligand in coordination chemistry and catalysis.

Chelating agent

metal complexes
2,6,2',6'-tetramethyl-[4,4']bipyrimidinyl can act as a chelating agent in metal complexes.

Catalyst

organic reactions
It can serve as a catalyst in various organic reactions.

Fluorescent probe

DNA and RNA structures
The compound can be used as a fluorescent probe to study the structures of DNA and RNA.

Importance

new materials and compounds development
Its specific properties and reactivity make it an important molecule in the development of new materials and compounds.

Upstream product

• 100-42-5 styrene 
• 16879-44-0 4-iodo-2,6-dimethylpyrimidine 

Relevant academic research and scientific papers

Studies on Pyrimidine Derivatives. XXX. The Palladium-Catalyzed Cross-Coupling Reaction of Iodopyrimidines with Terminal Olefinic Compounds

The influence of triphenylphosphine, used as a ligand, on the palladium-catalyzed cross-coupling reaction of iodopyrimidines with olefins such as ethyl acrylate, acrylonitrile, and styrene was investigated.In general, the addition of triphenylphosphine was concluded to retard the reaction in the pyrimidine series.The effect of triphenylphosphine in the monoazine series is also discussed.Keywords - palladium catalyst; carbon-carbon bond formation; homo-coupling reaction of N-heteroaromatic iodide; raction conditions; six-membered N-heteroaromatic iodide; substituted ethenylpyrimidine

Synthesis of pyrimidine derivatives having olefinic substituents by palladium-catalyzed cross-coupling reaction of iodopyrimidines

The palladium-catalyzed cross-coupling reactions of 2- and 4-iodopyrimidines with olefins were investigated on the stand-point of synthetic chemistry.The reaction was well catalyzed by use of palladium(II) acetate alone, palladium black, or palladium char