Category: 83-07-8

In an article, author is Jamali, Muhammad Fahad, once mentioned the application of 83-07-8, COA of Formula: C11H13N3O, Name is 4-Aminoantipyrine, molecular formula is C11H13N3O, molecular weight is 203.24, MDL number is MFCD00003145, category is pyrazoles-derivatives. Now introduce a scientific discovery about this category.

The Bestmann-Ohira Reagent and Related Diazo Compounds for the Synthesis of Azaheterocycles

Azaheterocycles are one of the most prevalent classes of compounds present in numerous bioactive compounds, natural products, and agrochemicals, and undoubtedly, new methods to access them are always in high demand. Among the methods available, the 1,3-dipolar cycloaddition reactions involving diazo compounds are particularly attractive because of their ability to rapidly construct densely functionalized azaheterocycles in a regioselective manner. In this context, the Bestmann-Ohira reagent has become a well-known reagent for the 1,3-dipolar cycloaddition reactions to produce phosphonylated heterocycles, besides its widespread use as a homologating agent for the conversion of aldehydes to alkynes. This account details our efforts toward broadening the synthetic utility of the Bestmann-Ohira reagent and related compounds for the preparation of azaheterocycles such as pyrazoles, spirooxindoles, triazoles, triazolines, and spiropyrazolines, emphasizing on domino multicomponent reactions employing readily available feedstock reagents.

If you are interested in 83-07-8, you can contact me at any time and look forward to more communication. COA of Formula: C11H13N3O.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 83-07-8, Name is 4-Aminoantipyrine, SMILES is O=C1N(C2=CC=CC=C2)N(C)C(C)=C1N, belongs to pyrazoles-derivatives compound. In a document, author is Amirnejat, Sara, introduce the new discover, Recommanded Product: 4-Aminoantipyrine.

Superparamagnetic Fe3O4@Alginate supported L-arginine as a powerful hybrid inorganic-organic nanocatalyst for the one-pot synthesis of pyrazole derivatives

Hybrid inorganic-organic material Fe3O4@Alg@CPTMS@Arg, was prepared by the layer-by-layer techniques through grafting l-arginine (l-arg) to Fe3O4@Alg using 3-chloropropyltrimethoxysilane (CPTMS) as a linker. Fe3O4@Alg was prepared by in situ co-precipitation of iron (iii) and iron (ii) chloride in the presence alginate (Alg). The hybrid inorganic-organic material was characterized employing various techniques such as Fourier transform infrared (FTIR), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and vibrating sample magnetometer (VSM). The as-prepared Fe3O4@Alg@CPTMS@Arg nanoparticles mediated the synthesis of pyrazole derivatives withviaone-pot reaction between phenylhydrazine, malononitrile, and various aromatic aldehydes under reflux in ethanol. Recycled catalyst exhibited comparable efficacy after seven cycles. The high catalytic activity, excellent yields, as well as the recyclability of the hybrid nanomaterials with quantitative efficiency, are factors that render this environmentally benign procedure appealing.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 83-07-8 is helpful to your research. Recommanded Product: 4-Aminoantipyrine.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

83-07-8, Name is 4-Aminoantipyrine, molecular formula is C11H13N3O, belongs to pyrazoles-derivatives compound, is a common compound. In a patnet, author is Wassel, Mohammed M. S., once mentioned the new application about 83-07-8, Application In Synthesis of 4-Aminoantipyrine.

Novel adamantane-pyrazole and hydrazone hybridized: Design, synthesis, cytotoxic evaluation, SAR study and molecular docking simulation as carbonic anhydrase inhibitors

A series of pyrazole derivatives 4, 5, 6, 12, 13, 14 as well as hydrazone derivatives 7, 10, 11 were synthesized starting from adamantane-1-carbohydrazide as the bioactive core. All newly designed adamantane derivates were established by full characterized using different spectroscopic methods. The novel derivatives were investigated for their antitumor activity against three cell line MCF-7, HepG-2 and A549. They displayed good IC50 values ranged between 1.55 to 42.17 mu M in comparison to Doxorubicin (IC50 = 3.58-8.19 mu M). Surprisingly, adamantine derivatives revealed more sensitivity and selectivity to lung cancer cells (A549) with eight compounds (4, 5, 9a, 9b, 9c, 12, 13a and 14c) having IC50 less than or equal ten micromoles. The most promising three adamantane derivatives 9a, 12 and 13a with IC50 values less than 5 mu M were selected to study enzymatic assay for isoenzyme hCAIX and hCAXII. Also, pyrazole core 13a and 12 showed higher K-I values than hydrazone derivatives 9a with submicromolar between (0.085-0.527 mu M), in comparison to Acetazolamide (0.041-0.068 mu M). Compound 13a is the most promising derivatives with anti-proliferative (A549) (IC50 = 1.55 +/- 0.08 mu M) which showed CAIX/XII inhibitory activity (K-I = 0.085 and 0.14 mu M), respectively. Finally, molecular docking simulation was performed to determine the binding modes and possible interaction of the adamantane derivatives within the active site of 3IAI and 1JD0 for CAIX / XII respectively with low binding affinity. (C) 2020 Elsevier B.V. All rights reserved.

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, 83-07-8. The above is the message from the blog manager. Application In Synthesis of 4-Aminoantipyrine.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

Chemistry is traditionally divided into organic and inorganic chemistry. The former is the study of compounds containing at least one carbon-hydrogen bonds. 83-07-8, Name is 4-Aminoantipyrine, molecular formula is C11H13N3O, belongs to pyrazoles-derivatives compound, is a common compound. In a patnet, author is Abdolla, Noreldin S. Y., once mentioned the new application about 83-07-8, Computed Properties of C11H13N3O.

Bis-cyclometallated Ir(III) complexes containing 2-(1H-pyrazol-3-yl)pyridine ligands; influence of substituents and cyclometallating ligands on response to changes in pH

Bis-cyclometallated Ir(III) complexes containing 2-(1H-pyrazol-3-yl)pyridine ligands have been synthesised. Their absorption is almost unchanged with changes in pH however the emission intensities vary by a factor of up to three and the complexes have emission pK(a)s in the range 8.0 to 10.0. Substituents on the pyrazole have only a minor effect on the emission pK(a). Surprisingly the complexes with phenylpyrazole cyclometallated ligands 3aL(1-3) showed an intensity decrease with increasing pH (switch off) whilst the corresponding phenylpyridine ones 3cL(1-3) showed an increase in emission intensity with increasing pH. Putting electron-withdrawing CF3 substituents on the cyclometallating phenyls reduced the pK(a) of the complexes to 6.8-7.8, thereby extending the useful pK(a) range; however, in general it tended to reduce the magnitude of the change in emission intensity. Surprisingly the CF3-substituted complexes also showed a complete reversal in the direction of the intensity change when compared to their respective unsubstituted congeners.

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, 83-07-8. The above is the message from the blog manager. Computed Properties of C11H13N3O.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, such as the rate of change in the concentration of reactants or products with time. 83-07-8, Name is 4-Aminoantipyrine, formurla is C11H13N3O. In a document, author is Chen, Zhangpei, introducing its new discovery. Application In Synthesis of 4-Aminoantipyrine.

Ruthenium-catalyzed alpha-carbonyl sulfoxonium ylide annulations with aryl substituted pyrazoles via C-H/N-H bond functionalizations

An efficient method for the construction of various pyrazolo[5,1-a]isoquinolines has been achieved via Ru(ii)-catalyzed alpha-carbonyl sulfoxonium ylide annulations with aryl substituted pyrazoles. This oxidant-free transformation occurred through pyrazole-directed C-H activation, Ru-carbene insertion, and acid-promoted carbonyl condensation processes, enabling dual C-C and C-N bond formation. A broad substrate scope with respect to both coupling components worked efficiently with high yields.

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Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

Reference of 83-07-8, 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. 83-07-8, Name is 4-Aminoantipyrine, SMILES is O=C1N(C2=CC=CC=C2)N(C)C(C)=C1N, belongs to pyrazoles-derivatives compound. In a article, author is Bharathi, R., introduce new discover of the category.

In vitro and molecular docking studies of an anti-inflammatory scaffold with human peroxiredoxin 5 and tyrosine kinase receptor

A new series of 4-(3-(2-amino-3,5-dibromophenyl)-1-(4-substitutedbenzoyl)-4,5-dihydro-1H-pyrazol-5-yl)benzonitrile (4a-h) compounds were synthesized and evaluated for in-vitro anti-inflammatory activities. The spectral (IR, NMR) and elemental analyses data of the product indicated the formation of new pyrazoles 4a-h. Compound 4e exhibited potent anti-inflammatory property with 85.45 % inhibitions. This value was compared with standard didofenac sodium. This data is explained using molecular docking analysis of receptor-ligand binding. These results demonstrated that pyrazole derivatives are potential inhibitors of Human Peroxiredoxin 5 and Tyrosine kinase receptor in the treatment of inflammation related illness.

Reference of 83-07-8, 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 83-07-8 is helpful to your research.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

Synthetic Route of 83-07-8, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C¨CH bond functionalisation has revolutionised modern synthetic chemistry. 83-07-8, Name is 4-Aminoantipyrine, SMILES is O=C1N(C2=CC=CC=C2)N(C)C(C)=C1N, belongs to pyrazoles-derivatives compound. In a article, author is Abdel-Halim, Mohammad, introduce new discover of the category.

Discovery of trisubstituted pyrazolines as a novel scaffold for the development of selective phosphodiesterase 5 inhibitors

Celecoxib, is a selective cyclooxygenase-2 (COX2) inhibitor with a 1,5-diaryl pyrazole scaffold. Celecoxib has a better safety profile compared to other COX2 inhibitors having side effects of systemic hypertension and thromboembolic complications. This may be partly attributed to an off-target activity involving phosphodiesterase 5 (PDE5) inhibition and the potentiation of NO/cGMP signalling allowing coronary vasodilation and aortic relaxation. Inspired by the structure of celecoxib, we synthesized a chemically diverse series of compounds containing a 1,3,5-trisubstituted pyrazoline scaffold to improve PDE5 inhibitory potency, while eliminating COX2 inhibitory activity. SAR studies for PDE5 inhibition revealed an essential role for a carboxylic acid functionality at the 1-phenyl and the importance of the non-planar pyrazoline core over the planar pyrazole with the 5-phenyl moiety tolerating a range of substituents. These modifications led to new PDE5 inhibitors with approximately 20-fold improved potency to inhibit PDE5 and no COX-2 inhibitory activity compared with celecoxib. PDE isozyme profiling of compound 11 revealed a favorable selectivity profile. These results suggest that trisubstituted pyrazolines provide a promising scaffold for further chemical optimization to identify novel PDE5 inhibitors with potential for less side effects compared with available PDE5 inhibitors used for the treatment of penile erectile dysfunction and pulmonary hypertension.

Synthetic Route of 83-07-8, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 83-07-8 is helpful to your research.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 83-07-8, Name is 4-Aminoantipyrine, SMILES is O=C1N(C2=CC=CC=C2)N(C)C(C)=C1N, belongs to pyrazoles-derivatives compound. In a document, author is Feng, Chao, introduce the new discover, Formula: C11H13N3O.

Structural Elucidation and Supercapacitive Performance on a Mn(II)-Based MOF

Metal-organic frameworks (MOFs) have attracted more attention in the field of supercapacitors for their potential high performance. Herein, one new Mn-based MOF, [Mn(Hpzca)(2)](n) (1), has been obtained via one-step hydrothermal method with the ligand (H(2)pzca = 1H-pyrazole-4-carboxylic acid). After characterization, the Mn-MOF exhibits a 3D structure bridged through the carboxylic group, which has a {3(18)center dot 4(38)center dot 5(10)} topological structure. The supercapacitive performance has been tested in the three-electrode system; the results showed a high specific capacitance and a good cycling stability. Its maximum specific capacitance was 443 F g(-1) at 1 Ag1-, along with a high capacitance of 86% retained after 1000 cycles at a current density of 5 A g(-1) in the 6 M KOH solution.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 83-07-8 is helpful to your research. Formula: C11H13N3O.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

Chemistry is an experimental science, Recommanded Product: 83-07-8, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 83-07-8, Name is 4-Aminoantipyrine, molecular formula is C11H13N3O, belongs to pyrazoles-derivatives compound. In a document, author is Rao, Mandava Venkata Basaveswara.

In Silico and Biological Evaluation of N-(2-methoxyphenyl) Substituted Pyrazoles Accessed via a Sonochemical Method

In view of remarkable biological properties including anticancer activities of N-aryl pyrazoles we have explored N-(2-methoxyphenyl) substituted pyrazoles and related derivatives as potential cytotoxic agents. In silico methods were adopted to understand/predict the biochemical and physiological effects, toxicity, and biological profiles of these compounds thereby assessing the potential drug-likeness of the hit molecule. The target compounds were conveniently prepared via a sonochemical method involving the C-N bond forming reactions in the presence of CuI in DMSO. A library of N-aryl pyrazole derivatives were synthesized via coupling of iodoarenes with pyrazole whereas the use of other N-heteroarene such as imidazole and pyrrole in place of pyrazole afforded the corresponding product. The in vitro evaluation of all these compounds was carried out against MDAMB-231 and MCF-7 cell lines and subsequently against SIRT1. The pyrazole derivative 3 c showed encouraging growth inhibition of both MDAMB-231 and MCF-7 cell lines (59 and 48 % at 10 mu M, respectively) and inhibition of SIRT1 (IC50 similar to 6.21 +/- 0.42 mu M) in vitro. The molecular docking studies suggested H-bonding (involving OMe group), Van der Waals and hydrophobic interactions of 3 c with important amino acid residues in the catalytic domain of SIRT1. Overall, cell-based as well as enzyme assay, molecular modelling, in silico ADME/TOX prediction and in vitro stability studies suggested 3 c as a potential hit molecule.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 83-07-8. Recommanded Product: 83-07-8.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

Chemistry is an experimental science, Application In Synthesis of 4-Aminoantipyrine, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 83-07-8, Name is 4-Aminoantipyrine, molecular formula is C11H13N3O, belongs to pyrazoles-derivatives compound. In a document, author is Karrouchi, Khalid.

Synthesis, X-ray, spectroscopy, molecular docking and DFT calculations of (E)-N ‘-(2,4-dichlorobenzylidene)-5-phenyl-1H-pyrazole-3-carbohydrazide

(E)-N’-(2,4-dichlorobenzylidene)-5-phenyl-1H-pyrazole-3-carbohydrazide (E-DPPC) has been synthesized and characterized by FT-IR, H-1-NMR, ESI-MS, and single-crystal X-ray diffraction. The structures and properties of this new pyrazole-3-carbohydrazide derivative were studied in gas phase and aqueous solution by using Functional hybrid B3LYP/6-311++G** calculations in gas phase and in aqueous solution to study. Two stable structures (C1 and C2) with similar energies were found in the PES. C2 evidence a higher dipole moment and a volume contraction in solution attributed to the presence of donors and acceptors H bonds. Besides, the changes in orientation and direction of dipole moment vector in solution are attributed to the hydration of E-DPPC with water molecules. The repulsion existent between the negative MK, Mulliken and NPA charges on the N12 and 015 atoms explain the diminishing of N12-C14-015 angle from 123.77 degrees in gas phase to 123.03 degrees in solution. Nucleophilic sites are visibly observed on the acceptor H bonds groups (N10, 015 and N22 atoms) while on the N18-H21, N12-H13, C11-H23, C2-H3, C17-H20 bonds characteristics electrophilic sites were found, being the N18-H21 bond the most labile donor of H bond with the lowest MEP and bond order values. NBO calculations suggest that C2 is clearly most stable in solution than in gas phase. AIM studies show that C2 is stable in both media due to new H bonds formed. Harmonic force fields in both media were calculated together with the scaled force constants while the 102 vibration normal modes expected for C2 were completely assigned. The comparisons of experimental NMR and UV-visible spectra with the corresponding predicted evidence reasonable correlations. Docking results also displayed that E-DPPC possessed good binding profile against receptor molecule and interacted with core residues of target protein. (C) 2020 Elsevier B.V. All rights reserved.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 83-07-8, in my other articles. Application In Synthesis of 4-Aminoantipyrine.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics