Chemical research careers are more diverse than they might first appear, as there are many different reasons to conduct research and many possible environments. 26040-51-7, Name is Bis(2-ethylhexyl) 3,4,5,6-tetrabromophthalate, SMILES is O=C(OCC(CC)CCCC)C1=C(Br)C(Br)=C(Br)C(Br)=C1C(OCC(CC)CCCC)=O, in an article , author is Nadirova, Maryana A., once mentioned of 26040-51-7, Synthetic Route of 26040-51-7.
It was found that the reaction of 5-arylfurfurilamines with maleic anhydride leads to the formation of 6-aryl-3a,6-epoxyisoindole-7-carboxylic acids (the cyclic form), which in solution are in dynamic equilibrium with N-furfurylmaleinamides (the open form). During the esterification of these tautomeric mixtures with methanol in the presence of a catalytic amount of sulfuric acid, methyl esters of 5-aryl-7a-hydroxy-7-methoxy-3-oxo-2,3,3a,4,7,7a-hexahydro-1H-isoindole-4-carboxylic acids, unexpected cleavage products of the 3a,6-oxo bridge of the cyclic form, are formed diastereospecifically. The structure of the obtained products was confirmed by X-ray structural analysis.
One of the oldest and most widely used commercial enzyme inhibitors is aspirin, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. Interested yet? Keep reading other articles of 26040-51-7, you can contact me at any time and look forward to more communication. Synthetic Route of 26040-51-7.
Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com