Interesting scientific research on (2-Amino-5-nitrophenyl)(phenyl)methanone

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 1775-95-7. HPLC of Formula: https://www.ambeed.com/products/1775-95-7.html.

Chemical Research Letters, April 2021. Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 1775-95-7, Name is (2-Amino-5-nitrophenyl)(phenyl)methanone, molecular formula is C13H10N2O3, HPLC of Formula: https://www.ambeed.com/products/1775-95-7.html, belongs to isothiazole compound, is a common compound. In a patnet, author is Kletskov, A. V., once mentioned the new application about 1775-95-7.

Conjugates of ferrocene and 4,5-dichloroisothiazole were synthesized, where the ferrocene and isothiazole moieties are linked through various structural fragments. The acylation of ferrocene with 4,5-dichloroisothiazole-3-carbonyl chloride gave (4,5-dichloroisothiazol-3-yl) ferrocenyl ketone; the acylation of aminomethylferrocene furnished the corresponding amide. The esterification of ferrocene-1,1′-dicarboxylic acid with 4,5-dichloroisothiazol-3-yl-methanol resulted in the formation of the corresponding ester. The condensation of 1,1′-diacetylferrocene with 4,5-dichloroisothiazole-3-carbaldehyde afforded ferrocenophane containing 4,5-dichloroisothiazole moieties.

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 1775-95-7. HPLC of Formula: https://www.ambeed.com/products/1775-95-7.html.

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