Chemical research careers are more diverse than they might first appear, as there are many different reasons to conduct research and many possible environments. , Reference of 696-63-9, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 696-63-9, Name is 4-Methoxythiophenol, molecular formula is C7H8OS, belongs to phthalazine compound. In a document, author is Dmitrienko, Anton.
The aluminum(I) compound NacNacAl (NacNac=[ArNC(Me)CHC(Me)NAr](-), Ar=2,6-iPr(2)C(6)H(3),1) shows diverse and substrate-controlled reactivity in reactions with N-heterocycles. 4-Dimethylaminopyridine (DMAP), a basic substrate in which the 4-position is blocked, induces rearrangement of NacNacAl by shifting a hydrogen atom from the methyl group of the NacNac backbone to the aluminum center. In contrast, C-H activation of the methyl group of 4-picoline takes place to produce a species with a reactive terminal methylene. Reaction of1with 3,5-lutidine results in the first example of an uncatalyzed, room-temperature cleavage of an sp(2)C-H bond (in the 4-position) by an Al(I)species. Another reactivity mode was observed for quinoline, which undergoes 2,2 ‘-coupling. Finally, the reaction of1with phthalazine produces the product of N-N bond cleavage.
Reference of 696-63-9, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 696-63-9 is helpful to your research.
Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem