In 2010,Tumkevicius, Sigitas; Dodonova, Jelena; Kazlauskas, Karolis; Masevicius, Viktoras; Skardziute, Lina; Jursenas, Saulius published 《Synthesis and photophysical properties of oligoarylenes with a pyrrolo[2,3-d]pyrimidine core》.Tetrahedron Letters published the findings.Recommanded Product: 2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine The information in the text is summarized as follows:
The Pd-catalyzed Suzuki-Miyaura reaction of 2,4-dichloropyrrolo[2,3-d]pyrimidine with arylboronates was studied. Pd(OAc)2/dicyclohexyl(2-biphenyl)phosphine/K3PO4 was an efficient catalyst system to prepare 4-aryl-2-chloro- and 2,4-diarylpyrrolo[2,3-d]pyrimidines. Novel non-linear mols. consisting of a pyrrolo[2,3-d]pyrimidine core and aryl branches were elucidated as blue light-emitters with fluorescence quantum yields of 4-67% in THF solution The impact of an electron-withdrawing CO2CMe3 group attached to the pyrrole ring of pyrrolopyrimidines on optical properties is discussed. In addition to this study using 2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine, there are many other studies that have used 2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine(cas: 90213-66-4Recommanded Product: 2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine) was used in this study.
2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine(cas: 90213-66-4) belongs to pyrimidine. The pyrimidine ring system has wide occurrence in nature as substituted and ring fused compounds and derivatives, including the nucleotides cytosine, thymine and uracil, thiamine (vitamin B1) and alloxan. Recommanded Product: 2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine
Referemce:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia