Safety of 4-Cyano-4-((phenylcarbonothioyl)thio)pentanoic acid, In classical electrochemical theory, both the electron transfer rate and the adsorption of reactants at the electrode control the electrochemical reaction. 201611-92-9, Name is 4-Cyano-4-((phenylcarbonothioyl)thio)pentanoic acid, SMILES is CC(SC(C1=CC=CC=C1)=S)(C#N)CCC(O)=O, belongs to phthalazine compound. In a article, author is Shamsi-Sani, Mahnaz, introduce new discover of the category.
Butane-1-soltunic acid modified starch-coated gamma-Fe2O3 magnetic nanoparticles (gamma-Fe2O3 @starchn-butyl SO3H] was easily prepared through a ring opening reaction of 1,4-butane sultone with nanomagnetic gamma-Fe2O3 @starch. After structural studies, using FT-IR, SEM, XRD, TGA, TEM, EDX, VSM and also pH analysis the efficiency of this reagent in the preparation of tetrahydrobenzimidazo[2,1-b] quinazolin-1(2H)-ones and 2H-indazolo[2,1-b]phthalazine-triones was studied. Operational simpleness, high yields, short reaction times, wide applicability and simple recyclability of the catalyst employing an external magnet are the most important advantages of this methodology.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 201611-92-9. Safety of 4-Cyano-4-((phenylcarbonothioyl)thio)pentanoic acid.
Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem