Final Thoughts on Chemistry for C7H5BrO2

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 586-76-5. Quality Control of 4-Bromobenzoic acid.

New research progress on 586-76-5 in 2021. As an important bridge between the micro and macro material world, chemistry is one of the main methods and means for humans to understand and transform the material world. 586-76-5, Name is 4-Bromobenzoic acid, formurla is C7H5BrO2. In a document, author is WAMHOFF, H, introducing its new discovery. Quality Control of 4-Bromobenzoic acid.

The reaction of 2-(2,3-O-isopropylidene-5-O-trityl-beta-D-ribofuranosyl)acetonitrile (6) with isopentyl nitrite/NaH and subsequent tosylation of Na-oximino nitrile 7 gave protected 2-D-ribofuranosyl-2-(tosyloximino)acetonitriles 9alpha,beta as novel C-nucleoside precursors. Treatment of 9alpha,beta with ethyl 2-mercaptoacetate under basic conditions afforded epimeric ethyl 4-aminoisothiazole-5-carboxylate C-nucleosides 10alpha,beta. Cyclization of 10alpha,beta to the desired 3-D-ribofuranosylisothiazolo[4,5-d]pyrimidin-7(6H)-ones 14alpha,beta was accomplished by the reaction of 10alpha,beta with triethyl orthoformate and subsequent amminolysis. Deprotection of 14beta and 14alpha in 7% HCl/MeOH gave the title compound 3 and alpha-isomeric C-nucleoside 4 as monohydrochloride salt, respectively. The configuration of C-glycoside 9alpha was established by X-ray crystallography.

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 586-76-5. Quality Control of 4-Bromobenzoic acid.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com