Tag: M.W:100-200

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Computed Properties of C5H6N2O. Introducing a new discovery about 13327-27-0, Name is 6-Methylpyridazin-3(2H)-one

A number of pyridazinone derivatives bearing an arylpiperazinylalkyl chain were synthesized and tested icv in a model of acute nociception induced by thermal stimuli in mice (tail flick). The most interesting and potent compound in this series was 6a, which showed an ED50=3.5 mug, a value about 3-fold higher with respect to morphine by the same route of administration. When administered per os, 6a was 4-fold more potent than morphine in the same test, suggesting a significant bioavailability. The same compound also showed high potency in the hot plate test. The antinociceptive effect of 6a was completely reversed by pretreatment with yohimbine both in the hot plate test and in the tail flick test. This demonstrated the involvement of the adrenergic system, which was confirmed by in vitro radioligand binding studies.

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.Computed Properties of C5H6N2O, you can also check out more blogs about13327-27-0

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N299 – PubChem

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Product Details of 34253-02-6, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 34253-02-6, Name is Methyl pyridazine-3-carboxylate, molecular formula is C6H6N2O2

Rate constants for the reaction of six possible diazine monocarboxylates with diazodiphenylmethane (DDM) in ethanol, and also for the hydrolysis of the corresponding methyl carboxylate esters, have been determined at four selected temperatures.Correlations with sums of the Hammett ? constants for ring nitrogens treated as substituents, which are fairly satisfactory for the reaction with DDM at 30 deg C (rhoDDM = 0.64, log k0 = -1.54, r = 0.92, s = 0.12) and for ester hydrolysis (rhoEH = 2.28, log k0 = -3.36, r = 0.94, s = 0.36) are, however, excellent for the intercorrelation of the two reaction series (rhoDDM/rhoEH = 0.34, r = 0.99, s = 0.12).The reactivity of ortho- and para-diazine dicarboxylates in the reaction with DDM, in ethanol and dimethylformamide, has been investigated and compared with the corresponding reactions of ortho- and para-benzene- and pyridine-dicarboxylates.

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Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N803 – PubChem

Related Products of 13327-27-0, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 13327-27-0, Name is 6-Methylpyridazin-3(2H)-one, molecular formula is C5H6N2O. In a Article，once mentioned of 13327-27-0

In this work, we are interested in studying the effect of the addition of a heterocyclic organic compound derived from pyridazine named ethyl (6-methyl-3-oxopyridazin-2-yl) acetate (GK2) on inhibition of the corrosion of mild steel (C38) in a molar hydrochloric acid solution. This study was performed using the method of weight loss, potentiodynamic polarization and the electrochemical impedance spectroscopy (EIS). Gravimetric measurements indicate that the inhibitor has GK2 efficiency increases with the concentration to reach a maximum value of 83.1% at 10?3 M. In addition, studies revealed that the potentiodynamic polarization act as a mixed inhibitor with predominance at cathodic domain. EIS shows that increasing the concentration of the inhibitor leads to an increase of the charge transfer resistance and reducing the double layer capacitance. Effect of temperature was studied between 308 and 343 K and determination of adsorption and activation parameters is also discussed.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Related Products of 13327-27-0. In my other articles, you can also check out more blogs about 13327-27-0

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N309 – PubChem

In heterogeneous catalysis, the catalyst is in a different phase from the reactants. SDS of cas: 141-30-0, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 141-30-0, name is 3,6-Dichloropyridazine. In an article，Which mentioned a new discovery about 141-30-0

Abstract: Three structurally related ligands 3-chloro-6-(benzoimidazol-1-yl)pyridazine (L1), 3-chloro-6-(1,2,4-triazol-1-yl)pyridazine (L2) and 3,6-bis(imidazol-1-yl)pyridazine (L3) were designed and synthesized, and six new Zn(II), Co(II), Cu(II) and Cd(II) complexes, namely, [M(L1)2Cl2] [M = Zn (1) and Co (2)], [Cu(L2)2(NO3)2(H2O)] (3), [Cu(L2)2Cl2]? (4), [CuL3(CH3COO)2]? (5) and [CdL3(SCN)2]? (6) were synthesized and characterized by elemental analyses, IR spectra as well as single-crystal X-ray diffraction analysis. The analysis reveals that complexes 1, 2 and 3 have a mononuclear structure, 1 and 2 have a similar structure. Complex 3 features a 1D structure with intermolecular O?H?O hydrogen bonding interactions. Complex 4 shows a 1D chain structure with bridging Cl? ions. Complex 5 exhibits a 1D ladder structure. The 2D framework of 6 features are rectangular grid with a (4, 4) topology. Additionally, photoluminescence properties of ligands L1, L3 and complexes 1, 2 and 6 have been studied and discussed. Graphical Abstract: Six new metal-organic complexes were synthesized and structurally characterized, complexes 1, 2 and 3 have a mononuclear structure, complexes 4 and 5 show 1D chain structure, the 2D framework of 6 has a rectangle grid with a (4, 4) topology, moreover, photoluminescence properties of ligands L1, L3 and complexes 1, 2 and 6 have been studied and discussed. [Figure not available: see fulltext.].

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Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N1981 – PubChem

Electric Literature of 7145-60-0, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 7145-60-0, Name is 6-Chloro-N,N-dimethylpyridazin-3-amine,introducing its new discovery.

It is shown by means of the fixed-structure method, UV spectroscopy and dipole-moment method that the product of the reaction of 3,6-dichloropyridazine with hydrazine in solution in methanol and acetonitrile has the 3-chloro-6-hydrazinopyridazine structure.

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Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2030 – PubChem

Synthetic Route of 2164-61-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.2164-61-6, Name is Pyridazine-3-carboxylic acid, molecular formula is C5H4N2O2. In a Patent，once mentioned of 2164-61-6

The invention provides compounds of Formula (I) pharmaceutically acceptable salts, pro-drugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variable are defined herein. The compounds of the invention are useful for treating immunological and oncological conditions.

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 2164-61-6

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N471 – PubChem

18591-82-7, Name is 6-Methylpyridazin-3-amine, belongs to pyridazine compound, is a common compound. name: 6-Methylpyridazin-3-amineIn an article, once mentioned the new application about 18591-82-7.

The present invention provides a compound represented by the formula: wherein Q represents a fused heterocyclic group, X and Y are the same or different and each represent an optionally halogenated lower alkyl group, an optionally halogenated lower alkoxy group, etc. , or a salt thereof, as well as a herbicide comprising the compound or a salt thereof, which exhibits a significant effect for control of sulfonylurea herbicide-resistant weeds in paddy fields and can reduce the number of active ingredients in a combined preparation and a method of controlling sulfonylurea herbicide-resistant weeds which comprises using the same.

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Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N232 – PubChem

Related Products of 5096-73-1, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.5096-73-1, Name is 6-Chloropyridazine-3-carboxylic acid, molecular formula is C5H3ClN2O2. In a article，once mentioned of 5096-73-1

The invention discloses a 1, 2, 3, 4 – tetrahydroquinoline compound synthesis method, organic chemical synthesis technology field. The method in order to elemental iodine is the catalyst, borane as reducing agent, quinoline compound used for the catalytic reduction reaction. Compared with the prior synthesis method, the method of the invention the greatest characteristic is the use of inexpensive I2 As the catalyst, without the need of metal involved in the reaction, mild reaction conditions, high speed and high efficiency, high catalytic efficiency, simple operation, good selectivity, the conversion of the product is high, up to 80% or more, popularization and application value, and is favorable for industrial production. (by machine translation)

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 5096-73-1

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2040 – PubChem

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Formula: C4H2Cl2N2, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 141-30-0, Name is 3,6-Dichloropyridazine, molecular formula is C4H2Cl2N2

New alkylol derivatives are described, which belong to the class having the structure formula STR1 where R represents a 5 or 6 membered heterocyclic ring selected among pyridine, pyrimidine, pyrazine, pyridazine, thiophene, furan, thiazole which optionally may be substituted with one or more groups selected among alkyl, alkoxy, halogen, amide, hydroxy, methylthio, trifluoromethyl, cyano, carboxy and the corresponding alkyl esters and salts with alkali metals n is 2 X and X’ represent each a hydrogen atom or hydroxy group with the exception of both being hydrogen atom, and X’ may be hydroxyethoxy moiety m is 0 or 1 and the corresponding non-toxic pharmaceutically acceptable acid addition salts. The compounds of the formula I are endowed with an interesting antitussive activity and, at their active dose, practically they are free of undesired side effects.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Formula: C4H2Cl2N2, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 141-30-0, in my other articles.

Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N1324 – PubChem

141-30-0, Name is 3,6-Dichloropyridazine, belongs to pyridazine compound, is a common compound. Recommanded Product: 141-30-0In an article, once mentioned the new application about 141-30-0.

The chelating ligands 3-chloro-6-(3-pyridyl-1-pyrazolyl)pyridazine (pp-Cl) and 3,6-bis(3-pyridyl- 1-pyrazolyl)pyridazine (bppp), were prepared by the condensation of pyridylpyrazole and 3,6-dichloropyridazine. The mononuclear complexes [(eta6-arene)Ru(pp-Cl)Cl]+ {eta6-arene = C6H 6 (1); p-iPrC6H4Me (2)}, [(eta5-C 5Me5)M(pp-Cl)]+ {M = Rh (3); Ir (4)}, [(eta6-arene) Ru(bppp)Cl]+ {eta6-arene = C6H6 (5); piPrC 6H4Me (6)}, [(eta5-C5Me5)M(bppp)]+ {M =Rh (7); Ir (8)} as well as the binuclear complexes [{(eta6- arene)RuCl}2(bppp)]2+ {eta6 -arene =C6H6 (9); p-iPrC6H4Me (10)} and [{(eta5-C5Me 5)MCl}2(bppp)]2+ {M = Rh (11); Ir (12)} have been synthesized from 3-chloro-6-(3-pyridyl-1-pyrazolyl)pyridazine (pp-Cl) or 3,6-bis(3-pyridyl-1- pyrazolyl)pyridazine (bppp) and the corresponding dimers [(eta6-arene)Ru(mu- Cl)Cl]2 and [Cp*M(mu-Cl)Cl]2, respectively. All complexes were isolated as their hexafluorophosphate salts and characterized by IR, NMR, mass spectrometry and UV-visible spectroscopy. The molecular structures of [2]PF6 and [7]PF6 have been established by single crystal X-ray structure analysis. Indian Academy of Sciences.

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Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N1600 – PubChem