Application of 569-31-3, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 569-31-3, Name is 6,7-Dimethoxy-3H-1-isobenzofuranone,introducing its new discovery.
beta-Hydrastine (I) is an erythro compound, the chiral centres at C-1 and C-9 having R and S configurations respectively.Its conversion into the hitherto unknown threo-isomer by the reduction of the corresponding immonium derivative (II) with zinc and acetic acid has met with failure.Surprisingly, II with Zn/ AcOH regenerates beta-hydrastine.During this reduction II rather suffers reductive cleavage yielding the non-nitrogenous lactone, meconine (IV).Sodium borohydride and catalytic reductions of II also fail to afford the threo-isomer.The latter is found to be extremely unstable as revealed from Dreiding model because of the severe steric interaction between the axial hydrogen at C-4 and the C1′-C2’bond.Benzylic oxidation of beta-hydrastine (I) with MnO2, instead of producing the desired 4-oxo derivative (VI), gives 6,7-methylenedioxyisoquinoline arising out of cleavage at C1-C9 bond.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 569-31-3, and how the biochemistry of the body works.Application of 569-31-3
Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H3127O – PubChem