CCC1=NC2=C(N=C(N2[C@@H]2O[C@H](COC(C3=CC=CC=C3)(C3=CC=CC=C3)C3=CC=CC=C3)[C@H]3OC(C)(C)O[C@@H]23)[Si](C(C)C)(C(C)C)C(C)C)C(Cl)=N1

InChIKey=OLKWRVWJNZXBEF-KHEPCZJLSA-N

C43H53ClN4O4Si

753.46

Organic compounds

Benzenoids

Triphenyl compounds

Not available

Not available

Triphenyl compounds

Purine nucleosides Purines and purine derivatives Benzylethers Alkylarylsilanes Halopyrimidines Ketals N-substituted imidazoles Monosaccharides Aryl chlorides Heteroaromatic compounds 1,3-dioxolanes Oxolanes Organic metalloid salts Dialkyl ethers Azacyclic compounds Oxacyclic compounds Organochlorides Alkylsilanes Hydrocarbon derivatives Organonitrogen compounds Organopnictogen compounds

Aromatic heteropolycyclic compounds

Triphenyl compound - Purine nucleoside - Purine - Imidazopyrimidine - Benzylether - Alkylarylsilane - Ketal - Halopyrimidine - N-substituted imidazole - Aryl chloride - Pyrimidine - Monosaccharide - Aryl halide - Monocyclic benzene moiety - Meta-dioxolane - Azole - Imidazole - Heteroaromatic compound - Oxolane - Acetal - Oxacycle - Azacycle - Dialkyl ether - Ether - Organic metalloid salt - Organoheterocyclic compound - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organosilicon compound - Alkylsilane - Organooxygen compound - Organohalogen compound - Organic metalloid moeity - Organochloride - Organonitrogen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety.

Not available