Extracurricular laboratory: Discover of 2,2′-((4-Aminophenyl)azanediyl)diethanol sulfate

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 54381-16-7. Quality Control of 2,2′-((4-Aminophenyl)azanediyl)diethanol sulfate.

Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, Quality Control of 2,2′-((4-Aminophenyl)azanediyl)diethanol sulfate54381-16-7, Name is 2,2′-((4-Aminophenyl)azanediyl)diethanol sulfate, SMILES is NC1=CC=C(N(CCO)CCO)C=C1.O=S(O)(O)=O, belongs to phthalazines compound. In a article, author is Azarifar, Davood, introduce new discover of the category.

Tetrakis(acetonitrile)copper(I) Hexafluorophosphate as an Efficient Catalyst for the Synthesis of Triazolo[1,2-a]indazole-1,3,8-trione and 2H-indazolo[2,1-b]phthalazine-trione Derivatives

Tetrakis(acetonitrile) copper(I) hexafluorophosphate, [Cu(CH3CN)(4)]PF6, was explored as an efficient catalyst to promote the three-component reaction of aryl aldehydes, dimedone and urazole or phthalhydrazide to afford the corresponding triazolo[1,2-a]indazole-1,3,8-trione and 2H-indazolo[2,1-b]phthalazine-trione derivatives respectively in high yields. The reactions were conducted at 80-100 degrees C under solvent-free conditions. The catalyst was easily prepared from available and inexpensive materials and was quantitatively recovered from the reaction by simple filtration and reused for a number of cycles with almost consistent activity.

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 54381-16-7. Quality Control of 2,2′-((4-Aminophenyl)azanediyl)diethanol sulfate.

Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem