Simple exploration of 4′-Ethyl-[1,1′-biphenyl]-4-carbonitrile

Reference of 58743-75-2, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 58743-75-2.

Reference of 58743-75-2, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 58743-75-2, Name is 4′-Ethyl-[1,1′-biphenyl]-4-carbonitrile, SMILES is N#CC1=CC=C(C2=CC=C(CC)C=C2)C=C1, belongs to phthalazine compound. In a article, author is Abedini, Masoumeh, introduce new discover of the category.

Efficient synthesis of 2H-indazolo[2,1-b]phthalazine-trione derivatives using succinimidinium N-sulfonic acid hydrogen sulfate as a new ionic liquid catalyst

Succinimidinium N-sulfonic add hydrogen sulfate is prepared as a new ionic liquid and characterized with a variety of techniques including FT-IR,H-1 and C-13 NMR, SEM, mass spectra method as well as Hammett acidity function. After identification, this reagent was used as an efficient catalyst for the multi-component synthesis of 2H-indazolo[2,1-b]phthalazine-trione derivatives. The simple work-up, mild reaction conditions, excellent yields and relatively short reaction times are the notable advantages of this protocol. In addition, the ionic liquid could be recycled several times without appreciable reduction in its catalytic activity. (C) 2015 Elsevier B.V. All rights reserved.

Reference of 58743-75-2, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 58743-75-2.

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