Category: pyrazoles-derivatives

Application In Synthesis of Tin(II) oxalate. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: Tin(II) oxalate, is researched, Molecular C2O4Sn, CAS is 814-94-8, about Reducing the excessive interior space of SnO2@C nanotubes by encapsulating SnO2 nanowires for high lithium storage. Author is Tian, Qinghua; Chen, Yanbin; Zhang, Wei; Sui, Zhuyin; Yang, Li.

Herein, to reduce the excessive interior space of hollow SnO2@C nanotubes, a particular composite (SnO2 NWs@void@SnO2@C) consisting of SnO2@C nanotubes encapsulating SnO2 nanowires has been constructed through a carefully planned method. When assessed as an anode material for lithium-ion batteries, the as-prepared SnO2 NWs@void@SnO2@C exhibits excellent performance, revealing high capacities of 1164 and 683 mAh g-1 after 320 and even 1000 cycles at 200 and 1000 mA g-1, resp. Notably, the excellent performance is benefited from the synergistic effect of structure advantages of SnO2 NWs@void@SnO2@C such as one-dimensional wires-in-tubes nanostructure, carbon coating, thin shells, void free space, and large surface area. Also thus excellent performance endows SnO2 NWs@void@SnO2@C with great promising for an advanced anode material of lithium-ion batteries.

Different reactions of this compound(Tin(II) oxalate)Application In Synthesis of Tin(II) oxalate require different conditions, so the reaction conditions are very important.

Reference:
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The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 3-Hydroxy-3-phenylpropanenitrile( cas:17190-29-3 ) is researched.Application In Synthesis of 3-Hydroxy-3-phenylpropanenitrile.Ma, Da-You; Wang, De-Xian; Pan, Jie; Huang, Zhi-Tang; Wang, Mei-Xiang published the article 《Nitrile biotransformations for the synthesis of enantiomerically enriched β2-, and β3-hydroxy and -alkoxy acids and amides, a dramatic O-substituent effect of the substrates on enantioselectivity》 about this compound( cas:17190-29-3 ) in Tetrahedron: Asymmetry. Keywords: Rhodococcus nitrile hydratase biotransformation enantiomeric. Let’s learn more about this compound (cas:17190-29-3).

Rhodococcus erythropolis AJ270, a nitrile hydratase/amidase-containing microbial whole cell catalyst, is able to catalyze the hydrolysis of a number of β-hydroxy and β-alkoxy nitriles under very mild conditions. Both the efficiency and enantioselectivity of the biocatalysis, however, were strongly dependent upon the structures of both nitrile and amide substrates. When biotransformations of racemic 3-hydroxy-3-phenylpropionitrile and 2-hydroxymethyl-3-phenylpropionitrile gave low enantioselectivity, their O-methylated isomers underwent highly efficient and enantioselective biocatalytic reactions to afford highly enantioenriched β2- and β3-hydroxy amide and acid derivatives in excellent yield. The study has provided an example of simple and very convenient substrate engineering method to increase the enantioselectivity of the biocatalytic reaction.

《Nitrile biotransformations for the synthesis of enantiomerically enriched β2-, and β3-hydroxy and -alkoxy acids and amides, a dramatic O-substituent effect of the substrates on enantioselectivity》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(3-Hydroxy-3-phenylpropanenitrile)Application In Synthesis of 3-Hydroxy-3-phenylpropanenitrile.

Reference:
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So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Azizi, Najmedin; Rahimi, Zahra; Alipour, Masoumeh researched the compound: 3-Hydroxy-3-phenylpropanenitrile( cas:17190-29-3 ).Name: 3-Hydroxy-3-phenylpropanenitrile.They published the article 《A magnetic nanoparticle catalyzed eco-friendly synthesis of cyanohydrins in a deep eutectic solvent》 about this compound( cas:17190-29-3 ) in RSC Advances. Keywords: magnetic iron oxide catalyst aldehyde epoxide cyanation green chem. We’ll tell you more about this compound (cas:17190-29-3).

Magnetic Fe3O4 nanoparticles in deep eutectic solvents (DESs) have been regard as excellent catalysts for highly efficient cyanosilylation of various aldehydes and epoxides using trimethylsilyl cyanide TMSCN in high yields with excellent selectivity. Fe3O4 nanoparticles were synthesized and applied as a catalyst for the preparation of a wide variety of cyanohydrins (α-hydroxy nitriles and β-hydroxy nitriles) in readily available urea-choline chloride deep eutectic solvent DES as the most promising environmentally benign and cost-effective green solvent. Magnetic DES operates at very mild reaction conditions and can be easily recycled without significant loss of its catalytic activity.

《A magnetic nanoparticle catalyzed eco-friendly synthesis of cyanohydrins in a deep eutectic solvent》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(3-Hydroxy-3-phenylpropanenitrile)Name: 3-Hydroxy-3-phenylpropanenitrile.

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Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Category: pyrazoles-derivatives. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: Tin(II) oxalate, is researched, Molecular C2O4Sn, CAS is 814-94-8, about Nanosized Ce-doped SnO2 nanocomposites as perspective materials for adsorption semiconductor sensors. Author is Fedorenko, George V.; Oleksenko, Lyudmila P.; Maksymovych, Nelly P.; Ripko, Oleksandr P.; Skolyar, Galina I..

Nanosized Ce-containing materials based on SnO2 with Sb additives were obtained by a sol-gel method using tin (II) oxalate, hydrogen peroxide, antimony (III) chloride and cerium (III) acetate as precursors. The average particle sizes of the synthesized materials were found to be ca. 9 nm. It was shown that the sensors based on these nanocomposites exhibit high sensitivities to hydrogen microconcns. in air, long-term stabilities of their parameters and demonstrate a wide range of the detectable hydrogen concentration (44 – 935 ppm H2 in air).

《Nanosized Ce-doped SnO2 nanocomposites as perspective materials for adsorption semiconductor sensors》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(Tin(II) oxalate)Category: pyrazoles-derivatives.

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

HPLC of Formula: 25956-17-6. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate, is researched, Molecular C18H14N2Na2O8S2, CAS is 25956-17-6, about Decolorization of azo dyes in a heterogeneous persulfate system using FeS as the activator. Author is Li, Haijun; Tang, Chong; Wang, Min; Mei, Changgen; Liu, Na.

Textile effluents containing synthetic refractory azo dyes are one of the most important sources of water pollution. However, these kinds of refractory organic pollutants did not resist a persulfate (PS) oxidation process which was correctly activated. In this study, PS was activated by ferrous sulfide (FeS) in a heterogeneous system to break down azo dyes wastewater. The results showed that all five selected azo dyes were efficiently broken down using the PS/FeS system, except for DY 12, and more than 95% of azo dyes were decolored within 60 min. The decolorization efficiency of DR 81 in the PS/FeS system was comparable to PS activated with heat (60°C) or Fe2+, and was slightly superior to Fe0 powders under the same conditions. Quenching studies indicated that both SO4-• and •OH were formed in the FeS surface and diffused into the solution to facilitate the successive transformation of DR 81, the •OH reaction with DR 81 might the crucial reaction. The coexisting chelating agents in real azo dye effluents at high concentrations had a neg. influence on azo dye decolorization by PS/FeS. However, the superior factor of the PS/FeS system was the regenerability and reusability of the heterogeneous catalyst.

《Decolorization of azo dyes in a heterogeneous persulfate system using FeS as the activator》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate)HPLC of Formula: 25956-17-6.

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

COA of Formula: C5H5Cl2N3. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 2-Amino-4,6-dichloro-5-methylpyrimidine, is researched, Molecular C5H5Cl2N3, CAS is 7153-13-1, about Synthesis and structure-activity relationship studies of polysubstituted pyrimidines as inhibitors of immune-activated nitric oxide production. Author is Jansa, Petr; Holy, Antonin; Dracinsky, Martin; Kolman, Viktor; Janeba, Zlatko; Kmonickova, Eva; Zidek, Zdenek.

Based on the previous discovery of the inhibitory effect of the 5-substituted 2-amino-4,6-dichloropyrimidines on nitric oxide (NO) production in vitro, a series of novel pyrimidine derivatives, namely 4,6-dichloro-2-[(N,N-dimethylamino)methyleneamino]pyrimidines, 2,4-diamino-6-chloropyrimidines, and 2,4-diamino-6-(2-hydroxyethoxy)pyrimidines, were prepared bearing various substituents at the C-5 position on the pyrimidine, such as hydrogen, Me, Et, Pr, iso-Pr, propargyl, allyl, Bu, sec-Bu, Ph, benzyl, and fluorine. The intrinsic biol. potential of the prepared compounds was characterized by effects on the in vitro production of immune-activated NO in mouse peritoneal cells. All 5-substituted 4,6-dichloro-2-[(N,N-dimethylamino)methyleneamino]pyrimidines strongly inhibited NO production The IC50s were <5 μM in most cases. The highest inhibitory activity was observed for the 5-s-Bu analog (IC50 = 2.57 μM), the lowest one for 5-unsubstituted compound (IC50 = 11.49 μM). With the exception of the 5-fluoro-4,6-dichloro-2-[(N,N-dimethylamino)methyleneamino] derivative, all other compounds were devoid of cytotoxic effects. The hitherto obtained data suggest that the NO-inhibitory activity depends on the presence of the 2-amino-4,6-dichloropyrimidine scaffold. 《Synthesis and structure-activity relationship studies of polysubstituted pyrimidines as inhibitors of immune-activated nitric oxide production》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(2-Amino-4,6-dichloro-5-methylpyrimidine)COA of Formula: C5H5Cl2N3.

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

Safety of Tin(II) oxalate. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: Tin(II) oxalate, is researched, Molecular C2O4Sn, CAS is 814-94-8, about Na2SnO3 as a novel anode for high performance lithium storage and its electrochemical reaction mechanism. Author is Lu, Fan; Zeng, Weiying; Lin, Haifeng; Liu, Shengzhou; Tian, Xiaoqing; Yang, Jie; Li, Jumei; Yang, Yin.

Herein, Na2SnO3 is employed as an anode for rechargeable Li ion battery (LIB). The authors thoroughly studied the electrochem. performance of Na2SnO3 in comparison with the most commonly used Sn based oxides, such as SnO2 and Li2SnO3. Na2SnO3 is greatly superior to SnO2 and Li2SnO3 in terms of capacity, cycling stability and rate capability. Impressively, Na2SnO3 presents favorable specific capacity of 480 mA h g-1 at c.d. of 200 mA g-1 after 100 cycles and still delivers a capacity of 439 mA h g-1 at extremely large c.d. of 1000 mA g-1, which are leading the performance in anodes for LIBs. Ex situ SEM anal. of anodes after different cycles revealed the surface microstructure of anodes plays a critical role in determining cycling stability. The SEM results show big cracks on the surface of electrode for SnO2 after less 15 cycles and for Li2SnO3 after more 100 cycles, resulting from their severe volume change during charging-discharging process. However, Na2SnO3 electrode exhibits uniform surface morphol. after 100 cycles. It is concluded the Na2O” intrinsic matrix of Na2SnO3 combining with Li2O” formed from the conversion reaction can act as a mixture buffering matrix that contributes to keeping the electrochem. formed nanoscale Sn particles apart and preventing their agglomeration during Li-Sn alloy formation and decomposition, thus inhibiting the volume expansion and the capacity fading by maintaining the electrode integrity. The electrochem. reaction mechanism of Na2SnO3 with Li was studied by ex situ XRD technique. The findings in this study provide a new valuable anode for high-performance LIBs and an insightful viewpoint of developing anode materials with high electrochem. performance by introducing the electrochem. inactive intrinsic matrix.

《Na2SnO3 as a novel anode for high performance lithium storage and its electrochemical reaction mechanism》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(Tin(II) oxalate)Safety of Tin(II) oxalate.

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

Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Article, Journal of the American Chemical Society called Pd/GF-Phos-Catalyzed Asymmetric Three-component Coupling Reaction to Access Chiral Diarylmethyl Alkynes, Author is Zhao, Guofeng; Wu, Yi; Wu, Hai-Hong; Yang, Junfeng; Zhang, Junliang, which mentions a compound: 52287-51-1, SMILESS is BrC1=CC=C2OCCOC2=C1, Molecular C8H7BrO2, Application of 52287-51-1.

Herein, a Pd-catalyzed enantioselective three-component coupling of N-tosylhydrazone, aryl halide and terminal alkyne under mild conditions utilizing a novel chiral sulfinamide phosphine ligand (GF-Phos), which provided a facile access to chiral diarylmethyl alkynes, the useful synthons in organic synthesis as well as exists as skeleton in many bioactive mols. was reported. A pair of enantiomers of the product could be easily prepared using the same chiral ligand by simply changing the aryl substituents of the N-tosylhydrazone, aryl halide. The salient features of this reaction included the readily available starting materials, general substrate scope, high enantioselectivity, ease of scale up, mild reaction conditions and versatile transformations.

《Pd/GF-Phos-Catalyzed Asymmetric Three-component Coupling Reaction to Access Chiral Diarylmethyl Alkynes》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(6-Bromo-2,3-dihydrobenzo[b][1,4]dioxine)Application of 52287-51-1.

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

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate, is researched, Molecular C18H14N2Na2O8S2, CAS is 25956-17-6, about Rapid screening of 70 colorants in dyeable foods by using ultra-high-performance liquid chromatography-hybrid quadrupole-Orbitrap mass spectrometry with customized accurate-mass database and mass spectral library, the main research direction is colorant dyeable food rapid screening; Accurate-mass database; Colorants; Dyeable foods; Hybrid quadrupole–Orbitrap mass spectrometry; Mass spectral library; Ultra-high-performance liquid chromatography.Related Products of 25956-17-6.

A rapid screening method of 70 colorants for regulatory control in dyeable foods was established using ultra-high-performance liquid chromatog.-hybrid quadrupole-Orbitrap mass spectrometry (UHPLC-Q/Orbitrap MS) with customized accurate-mass database and mass spectral library. A rapid, high-throughput, and simple sample pretreatment condition with low reagent consumption and high recovery was developed on the basis of ultrasound-assisted extraction and dispersion solid-phase extraction Rapid screening was conducted by comparing the exptl. measured exact mass of the parent and fragment ions, the isotope pattern, and the retention time with the accurate-mass database and by matching the acquired MS/MS spectra against the mass spectral library. The performance of the method was evaluated in terms of linearity, limits of detection, limits of quantitation, recovery, repeatability, reproducibility, and matrix effect. The proposed method was applied for simultaneous anal. of 70 colorants in seven kinds of dyeable foods, and it exhibited great potential for broad, sensitive, and reliable.

《Rapid screening of 70 colorants in dyeable foods by using ultra-high-performance liquid chromatography-hybrid quadrupole-Orbitrap mass spectrometry with customized accurate-mass database and mass spectral library》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate)Related Products of 25956-17-6.

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

Application In Synthesis of 3-Hydroxy-3-phenylpropanenitrile. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: 3-Hydroxy-3-phenylpropanenitrile, is researched, Molecular C9H9NO, CAS is 17190-29-3, about A high throughput screening strategy for the assessment of nitrile-hydrolyzing activity towards the production of enantiopure β-hydroxy acids. Author is Coady, Tracey M.; Coffey, Lee V.; O’Reilly, Catherine; Owens, Erica B.; Lennon, Claire M..

Nitrile hydrolyzing enzymes have found wide use in the pharmaceutical industry for the production of fine chems. This work presents a strategy that facilitates the rapid identification of bacterial isolates demonstrating nitrile hydrolyzing activity. The strategy incorporates toxicity, starvation and induction studies along with subsequent colorimetric screening for activity, further focusing the assessment towards the substrates of interest. This high-throughput strategy uses a 96 well plate system, and has enabled the rapid biocatalytic screening of 256 novel bacterial isolates towards β-hydroxynitriles. Results demonstrate the strategy’s potential to rapidly assess a variety of β-hydroxynitriles including aliphatic, aromatic and dinitriles. A whole cell catalyst Rhodococcus erythropolis SET1 was identified and found to catalyze the hydrolysis of 3-hydroxybutyronitrile with remarkably high enantioselectivity under mild conditions, to afford (S)-3-hydroxybutyric acid in 42% yield and >99.9% ee. The biocatalytic capability of this strain including the variation of parameters such as temperature and time were further investigated and all results indicate the presence of a highly enantioselective if not enantiospecific nitrilase enzyme within the microbial whole cell.

《A high throughput screening strategy for the assessment of nitrile-hydrolyzing activity towards the production of enantiopure β-hydroxy acids》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(3-Hydroxy-3-phenylpropanenitrile)Application In Synthesis of 3-Hydroxy-3-phenylpropanenitrile.

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