Category: pyridazines

Reference of 73963-42-5, 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. 73963-42-5, Name is 5-(4-Chlorobutyl)-1-cyclohexyl-1H-tetrazole, SMILES is ClCCCCC1=NN=NN1C2CCCCC2, belongs to pyridazines compound. In a article, author is Nahle, Ayssar, introduce new discover of the category.

Effect of substituted methyl group by phenyl group in pyridazine ring on the corrosion inhibition of mild steel in 1.0 M HCl

Purpose – The purpose of this paper is to study the inhibition effect of (6-phenyl-3-oxopyridazin-2-yl) acetohydrazide (GP4) on the corrosion of mild steel in acidic medium by gravimetric measurements, potentiodynamic polarization, and electrochemical impedance spectroscopy (EIS). Design/methodology/approach – Weight loss measurements, potentiodynamic tests and EIS were performed during this study. Findings -(6-phenyl-3-oxopyridazin-2-yl) acetohydrazide (GP4) was found to be a very efficient inhibitor for mild steel in 1.0 M HCl solution, reaching about 85 per cent with inhibitor concentration 1.0 x 10-3 M at 303 K. Practical implications -(6-phenyl-3-oxopyridazin-2-yl) acetohydrazide (GP4) was found to play an important role in the corrosion inhibition of mild steel in acidic solution. Originality/value – This paper is intended to be added to the family of pyridazine derivatives which are highly efficient inhibitors and can be used in the area of corrosion prevention and control.

Reference of 73963-42-5, 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 73963-42-5 is helpful to your research.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem

 

Reference of 375395-33-8, 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. 375395-33-8, Name is N-Methyl-N,N-dioctyloctan-1-aminium bis((trifluoromethyl)sulfonyl)amide, SMILES is CCCCCCCC[N+](CCCCCCCC)(C)CCCCCCCC.O=S([N-]S(=O)(C(F)(F)F)=O)(C(F)(F)F)=O, belongs to pyridazines compound. In a article, author is Breidung, Juergen, introduce new discover of the category.

Equilibrium Structures of Pyrazine, s-Triazine, and s-Tetrazine

In recent years, accurate equilibrium (r(e)) structures have been determined for pyridine, pyridazine, and pyrimidine. Here, we report accurate r(e) structures for the structurally related molecules pyrazine, s-triazine, and s-tetrazine, which were obtained using a composite approach based on explicitly correlated coupled-cluster theory (CCSD(T)-F12b) in conjunction with a large correlation-consistent basis set (cc-pCVQZ-F12) to take core-valence electron correlation into account. Additional terms were included to correct for the effects of iterative triple excitations (CCSDT), noniterative quadruple excitations (CCSDT-(Q)), and scalar relativistic contributions (DKH2-CCSD(T)). The performance of this computational procedure was established through test calculations on selected small molecules. For s-triazine, accurate experimental ground-state rotational constants (B-0) of the parent molecule and six D-3h isotopologues from the literature were used to determine a semiexperimental r(e) structure, which was found to be essentially identical with the best estimate from the current composite approach. The presently recommended equilibrium structural parameters of s-triazine are r(e)(CH) = 108.17 pm, r(e)(CN) = 133.19 pm, and theta(e)(NCN) = 125.95 degrees, with estimated uncertainties of +/- 0.10 pm and +/- 0.10 degrees, respectively. The predicted equilibrium geometries for pyrazine and s-tetrazine are expected to be of the same accuracy. We recommend for pyrazine: r(e)(CH) = 108.16 pm, r(e)(CN) = 133.34 pm, r(e)(CC) = 139.07 pm, theta(e)(CNC) = 115.60 degrees, and theta(e)(HCC) = 120.75 degrees; and for s-tetrazine: r(e)(CH) = 107.95 pm, r(e)(CN) = 133.39 pm, r(e)(NN) = 132.01 pm, and theta(e)(NCN) = 126.59 degrees.

Reference of 375395-33-8, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 375395-33-8.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem

 

Chemistry, like all the natural sciences, Formula: C7H6F3N, begins with the direct observation of nature¡ª in this case, of matter.88-17-5, Name is 2-(Trifluoromethyl)aniline, SMILES is NC1=CC=CC=C1C(F)(F)F, belongs to pyridazines compound. In a document, author is Feraldi-Xypolia, Alexandra, introduce the new discover.

Synthesis of -(Trifluoromethyl)pyridazine Derivatives

Over the last decades, an increasing interest in -(trifluoromethyl)pyridazines in medicinal chemistry has been noticed. This interest stems firstly from the recent development of biologically active pyridazines as well as from the capacity of the pyridazine ring to be a bioisoster of other heterocycles. Secondly, due to the influence of a fluorine atom on the chemical and physico-chemical properties of organic compounds, fluorinated pyridazines have been an attractive scaffold for medicinal chemists. Consequently, the methods that allow the synthesis of fluorinated pyridazines, and more specifically pyridazines possessing either one or two CF3 groups to the nitrogen atoms, are of great interest and are reported in this review.

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 88-17-5. Formula: C7H6F3N.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem

 

Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics, COA of Formula: CH6N4S, 2231-57-4, Name is Carbonothioic dihydrazide, SMILES is NNC(NN)=S, belongs to pyridazines compound. In a document, author is Hasegawa, Takeshi, introduce the new discover.

A Systematic Analysis of the Binding Affinity between the Pim-1 Kinase and Its Inhibitors Based on the MM/3D-RISM/KH Method

A systematic study of the binding affinities of 16 lead compounds targeting the Pim-1 kinase based on the 3DRISM/KH theory and MD simulations is reported. The results show a correlation coefficient R = 0.69 between the theoretical and experimental values of the binding free energy. This demonstrates that the method is applicable to the problem of compound screening and lead optimization, for which relative values of the free energy among the compounds have significance. We elucidate the contribution of the ligand fragments to the binding free energy. Our results indicate that the interactions between the residues and the triazolo[4,3-b]pyridazine scaffold as well as the phenyl ring of the ligand molecule make significant contributions to stabilization of the complex. Using the 3D-RISM/KH theory, we further analyze the probability distribution of a ligand fragment around the protein ligand complex in which the substituent around the phenyl ring is removed from the ligand. The results demonstrate that the 3D-RISM/KH theory is capable of predicting the position of substitution on a ligand that has a higher affinity to a target protein.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 2231-57-4. COA of Formula: CH6N4S.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem

 

Electric Literature of 375395-33-8, Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 375395-33-8, Name is N-Methyl-N,N-dioctyloctan-1-aminium bis((trifluoromethyl)sulfonyl)amide, SMILES is CCCCCCCC[N+](CCCCCCCC)(C)CCCCCCCC.O=S([N-]S(=O)(C(F)(F)F)=O)(C(F)(F)F)=O, belongs to pyridazines compound. In a article, author is Yengoyan, Aleksandr P., introduce new discover of the category.

Synthesis of novel 6-(3,5-dimethyl-1H-pyrazol-1-yl)pyridazin-3(2H)-one derivatives and their preliminary biological evaluation

Simple and accessible pathways for the synthesis of a series of novel 6-(3,5-dimethyl-1H-pyrazol-1-yl)pyridazin-3(2H)-one derivatives including compounds with a combination of a pyrazolyl-pyridazine moiety with pyrimidine, 1,3,5-triazine and 1,3,4-oxadiazole rings in the same molecules were established. The tautomeric structures of 3-oxopyridazine and 5-thioxo-1,3,4-oxadiazole rings and also the position of their alkylation were shown. At preliminary screening the synthesised compounds showed pronounced plant growth stimulant activity. The most active compounds were selected for deeper studies and further field trials.

Electric Literature of 375395-33-8, 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 375395-33-8.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem

 

In an article, author is Sadimenko, Alexander P., once mentioned the application of 375-72-4, Name is 1,1,2,2,3,3,4,4,4-Nonafluorobutane-1-sulfonyl fluoride, molecular formula is C4F10O2S, molecular weight is 302.0906, MDL number is MFCD00007422, category is pyridazines. Now introduce a scientific discovery about this category, Name: 1,1,2,2,3,3,4,4,4-Nonafluorobutane-1-sulfonyl fluoride.

Organometallic Complexes of Azines

Organometallic complexes of practically unsubstituted (non-chelating) azines and their benzannulated derivatives, possible N-heterocyclic carbenes containing at least one double bond, and boron-, boronenitrogen, silicon-, tri- and hexaphosphorus analogs of azines are considered in the view of their synthetic availability, coordination modes, and possible application in catalysis and materials chemistry.

Do you like my blog? If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 375-72-4, Name: 1,1,2,2,3,3,4,4,4-Nonafluorobutane-1-sulfonyl fluoride.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem

 

Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 103-85-5, Name is 1-Phenylthiourea, SMILES is S=C(N)NC1=CC=CC=C1, in an article , author is Olejniczak, Anna, once mentioned of 103-85-5, Recommanded Product: 1-Phenylthiourea.

Crystal design by CH center dot center dot center dot N and N center dot center dot center dot N interactions: high-pressure structures of high-nitrogen-content azido-triazolopyridazines compounds

High-nitrogen-content compounds 6-azido-1,2,4-triazolo[4,3-b]pyridazine (C5H3N7) and its 3-methyl derivative (C6H5N7) have been in situ crystallized in a diamond-anvil cell and their structures determined by single-crystal X-ray diffraction. Under ambient and high-pressure conditions the crystallizations yield the same phases: the C5H3N7 anhydrate and C6H5N7 hydrated clathrate. In both the structures there are clearly distinguished regions of short CH center dot center dot center dot N and N center dot center dot center dot N intermolecular contacts, the latter involving exclusively the azide groups. High pressure initially increases the contents of water in the channel pores of the clathrate.

But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 103-85-5, you can contact me at any time and look forward to more communication. Recommanded Product: 1-Phenylthiourea.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem

 

Reference of 19430-93-4, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C¨CH bond functionalisation has revolutionised modern synthetic chemistry. 19430-93-4, Name is 3,3,4,4,5,5,6,6,6-Nonafluorohex-1-ene, SMILES is C=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)F, belongs to pyridazines compound. In a article, author is Kocak, Ramazan, introduce new discover of the category.

Synthesis of Pyridazine and Pyrrole Analogues of 2-Aminotetralin as Potential Dopaminergics

Syntheses of pyridazine and pyrrole analogues of 2-aminotetralin starting from 3-cyclohexene-1-carboxylic acid are reported. All syntheses involve the following key steps: Curtius rearrangement for amine functionality, inverse electron demand Diels-Alder addition with 1,2,4,5-tetrazine for pyridazine ring synthesis, and pyridazine-to-pyrrole ring contraction for pyrrole ring formation.

Reference of 19430-93-4, 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 19430-93-4 is helpful to your research.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem

 

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels. 1538-08-5, Name is 2,2,2-Trifluoroacetohydrazide, molecular formula is C2H3F3N2O. In an article, author is Mondal, Sandip,once mentioned of 1538-08-5, Application In Synthesis of 2,2,2-Trifluoroacetohydrazide.

A Redox-Active Cascade Precursor: Isolation of a Zwitterionic Triphenylphosphonio-Hydrazyl Radical and an Indazolo-Indazole Derivative

A redox-active [ML] unit (M = Co-II and Mn-II; LH2 = N’-(1,4-dioxo-1,4-dihydronaphthalen-2-y1)benzohydrazide) defined as a cascade precursor that undergoes a multicomponent redox reaction comprising of a C-N bond formation, tautomerization, oxidation, C-C coupling, demetalation, and affording 6,14-dibenzoylbenzo[f]benzo [5,6] in dazolo [3a,3-c] indazole-5,8,13,16-tetraone (L-Ind(2)) is reported. Conversion of LH2 -> L-Ind(2) in air is overall a (6H(+)+6e) oxidation reaction, and it opens a route for the syntheses of bioactive diarylindazolo [3a,3-c]indazole derivatives. The reaction occurs via a radical coupling reaction, and the radical intermediate was isolated as a triphenylphosphonio adduct. In presence of PPh3 the [ML] unit promotes a reaction that involves a C-P bond formation, tautomerization, and oxidation to yield a stable zwitterionic triphenylphosphonio-hydrazyl radical (L-PPh3(+/-center dot)). Conversion of LH2 -> L-PPh3(+/-center dot) is a (3H(+)+3e) oxidation reaction. To authenticate the [ML], unit, in addition to the L-Ind(2) a zinc(II) complex, [(L-3)Zn-II(H2O)Cl]center dot 2Me0H (1.2MeOH), was successfully isolated (L3H = a pyridazine derivative of 1,4 naphthoquinone) from a reaction of LH2 with hydrated ZnCl2. Conversion of 3LH(2) -> 1 is also a multicomponent (6H(+)+6e) oxidation reaction promoted by zinc(II) ion via a radical intermediate. Facile oxidation of [L2-] to [L.-] that was considered as an intermediate of these conversions was confirmed by isolating a 1,4 naphthoquinone-benzhydrazyl radical (LH.) complex, [(LH center dot)Zn-II(H2O)Cl-2] (2H(center dot)). The intermediates of LH2 -> L-Ind(2), LH2 -> L-PPh3(+/-center dot), and 3LH(2) -> 1 conversions were analyzed by electrospray ionization mass spectroscopy. The molecular and electronic structures of L-PPh3(+/-center dot) (Ind)L2, 1.2MeOH, and 2H(center dot) were confirmed by single-crystal X-ray crystallography, electron paramagnetic resonance spectroscopy, and density functional theory calculations.

Interested yet? Keep reading other articles of 1538-08-5, you can contact me at any time and look forward to more communication. Application In Synthesis of 2,2,2-Trifluoroacetohydrazide.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem

 

Let¡¯s face it, organic chemistry can seem difficult to learn. Especially from a beginner¡¯s point of view. Like 103-85-5, Name is 1-Phenylthiourea. In a document, author is Thakkar, Ajit J., introducing its new discovery. Recommanded Product: 103-85-5.

Dipole oscillator strength distributions, sum rules, mean excitation energies, and isotropic van der Waals coefficients for benzene, pyridazine, pyrimidine, pyrazine, s-triazine, toluene, hexafluorobenzene, and nitrobenzene

Experimental, theoretical, and additive-model photoabsorption cross sections combined with constraints provided by the Kuhn-Reiche-Thomas sum rule and the high-energy behavior of the dipole oscillator strength density are used to construct dipole oscillator strength distributions for benzene, pyridazine (1,2-diazine), pyrimidine (1,3-diazine), pyrazine (1,4-diazine), s-triazine (1,3,5-triazine), toluene (methylbenzene), hexafluorobenzene, and nitrobenzene. The distributions are used to predict dipole sum rules S(k) for -6 <= k <= 2, mean excitation energies I(k) for -2 <= k <= 2, and isotropic van der Waals C-6 coefficients. A popular combination rule for estimating C-6 coefficients for unlike interactions from the C-6 coefficients of the like interactions is found to be accurate to better than 1% for 606 of 628 cases (96.4%) in the test set. I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 103-85-5 help many people in the next few years. Recommanded Product: 103-85-5.

Reference:
Pyridazine – Wikipedia,
,Pyridazine | C4H4N2 – PubChem