Category: 108-36-1

Chemo-enzymatic cascade processes are invaluable due to their ability to rapidly construct high-value products from available feedstock chemicals in a one-pot relay manner. In an article, author is Ghorbani-Vaghei, Ramin, once mentioned the application of 108-36-1, Name is 1,3-Dibromobenzene, molecular formula is C6H4Br2, molecular weight is 235.904, MDL number is MFCD00000078, category is phthalazines. Now introduce a scientific discovery about this category, Application In Synthesis of 1,3-Dibromobenzene.

Preparation and characterization of nanomagnetic piperidinium benzene-1,3-disulfonate ionic liquid as a novel, green and heterogeneous catalyst and its use in the synthesis of 1H-pyrazolo[1,2-b]phthalazine-5,10-diones and 1H-pyrazolo[1,2-a]pyridazine-5,8-diones under solvent-free conditions

The one-pot four-component synthesis of 1H-pyrazolo[1,2-b] phthalazine-5,10-diones and 1H-pyrazolo[1,2-a] pyridazine-5,8-diones was carried out from the reaction between various aldehydes, malononitrile, hydrazine hydrate and phthalic anhydride or maleic anhydride at 110 degrees C in solvent-free conditions using piperidinium benzene-1,3-disulfonate nanomagnetic ionic liquid (NMIL) as a novel and reusable catalyst. Some advantages of the presented procedure are a significant reduction in cost, effective catalysis and reusability of the catalyst. NMIL was thoroughly characterized using Fourier transform infrared spectroscopy, X-ray diffraction, scanning and transmission electron microscopies, thermogravimetry, derivative thermogravimetry, Brunauer-Emmett-Teller analysis, vibrating sample magnetometry and energy-dispersive X-ray spectroscopy. The technique is developed as a suitable and safe method for the synthesis of 1H-pyrazolo[1,2-b] phthalazine-5,10-diones and 1H-pyrazolo[1,2-a] pyridazine-5,8-diones making use of an efficient and reusable green catalyst.

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

Electric Literature of 108-36-1, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice of redox mediator can avoid electrode passivation and overpotential. 108-36-1, Name is 1,3-Dibromobenzene, SMILES is BrC1=CC(Br)=CC=C1, belongs to phthalazines compound. In a article, author is El-Faham, Ayman, introduce new discover of the category.

Crystal structure of (E)-1-(2-(thiophen-2-ylmethylene)hydrazinyl)phthalazine hydrochloride-ethanol (1/1), C15H17ClN4OS

C15H17ClN4OS, triclinic, P1 (no. 2), a = 7.5069(2) angstrom, b = 9.4329(3)angstrom, c = 11.9723(4)angstrom, beta = 81.6963(11)degrees, gamma = 78.2307(9)degrees, g = 86.700(1)degrees, V = 820.91(4) angstrom(3), Z = 2, R-gt(F) = 0.0621, wR(ref)(F-2) = 0.1923, T = 100 K.

Electric Literature of 108-36-1, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about 108-36-1 is helpful to your research.

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

Related Products of 108-36-1, 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. 108-36-1, Name is 1,3-Dibromobenzene, SMILES is BrC1=CC(Br)=CC=C1, belongs to phthalazines compound. In a article, author is Mousapour, Maryam, introduce new discover of the category.

Efficient Synthesis of 2H-Indazolo[2,1-b]Phthalazine-Triones Using [PVPH]ClO4 as a Modified Polymeric Catalyst

In this work, poly(vinylpyrrolidonium) perchlorate {[PVPH]ClO4}, a newly reported modified polymeric catalyst, is used as an efficient and reusable solid acid catalyst for the promotion of the synthesis of 2H-indazolo[2,1-b]phthalazine-trione derivatives. All reactions were performed under mild conditions and the products were formed over short reaction times in excellent yields. It is important to note that this solid acid catalyst can be reused several times without any appreciable loss in its activity.

Related Products of 108-36-1, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 108-36-1 is helpful to your research.

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