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《Polarographic investigation of halogen atom mobility in the halosubstituted components of nucleic acids》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(8-Bromoguanine)Name: 8-Bromoguanine.

Name: 8-Bromoguanine. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 8-Bromoguanine, is researched, Molecular C5H4BrN5O, CAS is 3066-84-0, about Polarographic investigation of halogen atom mobility in the halosubstituted components of nucleic acids. Author is Kadysh, V. P.; Kaminskii, Yu. L.; Rumyantseva, L. N.; Efimova, V. L.; Stradinsh, J. P..

Reduction potentials for a series of bromo and iodo derivatives of nucleic acid components were determined in buffered solutions (pH 1.0, concentration 5 × 10-4 M/L) in an interval of -0.5…-1.8 V. Iodo derivatives were more easily reduced (500-800 MV) than the corresponding bromo derivatives

《Polarographic investigation of halogen atom mobility in the halosubstituted components of nucleic acids》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(8-Bromoguanine)Name: 8-Bromoguanine.

Reference:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem