Reference of 2,3,5-Trichloropyridin-4-ol. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 2,3,5-Trichloropyridin-4-ol, is researched, Molecular C5H2Cl3NO, CAS is 1970-40-7, about Inhibition of photosynthesis by pyriclor. Author is Meikle, Richard W..
The effect of pyriclor on some photochem. reactions that bring about the formation of assimilatory power, the generation of ATP and NADPH, at the expense of radiant energy was determined by using isolated Spinacia oleracea var Viroflay (spinach) chloroplasts. The assimilation of CO2 and cyclic photophosphorylation catalyzed by FMN both showed inhibition at a rather high level of pyrichlor; however, O evolution and noncyclic photophosphorylation were strongly inhibited. Evidence is presented to support the conclusion that the locus of attack is the O-evolving system and (or) Pigment System 2 of the photosynthetic apparatus
Although many compounds look similar to this compound(1970-40-7)Reference of 2,3,5-Trichloropyridin-4-ol, numerous studies have shown that this compound(SMILES:OC1=C(Cl)C(Cl)=NC=C1Cl), has unique advantages. If you want to know more about similar compounds, you can read my other articles.
Reference:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem