Category: 119-61-9

Safety of Benzophenone. Recently I am researching about OXIDATIVE STRESS; MODEL, Saw an article supported by the . Published in PHARMACOTHERAPY GROUP in BENIN CITY ,Authors: Saleem, MF; Khan, MA; Ahmad, I; Aslam, N; Khurshid, U. The CAS is 119-61-9. Through research, I have a further understanding and discovery of Benzophenone

Purpose: To synthesize and characterize some new gabapentin Schiff base derivatives, and to assess their antibacterial, antioxidant and antiepileptic activities. Methods: Four Schiff base derivatives of gabapentin, termed G1, G2, G3 and G4, were synthesized by condensation with benzoin, vanillin, acetophenone, and benzophenone, respectively. Their chemical identities were established by FTIR, H-1 NMR and C-13 NMR techniques. The new compounds were screened for antibacterial activity using agar well method, antioxidant activity by DPPH assay, and anticonvulsant activity against pentylenetetrazole (PTZ) induced seizures in mice. Results: All the compounds showed antibacterial activity against the test strains to variable degrees, while the parent drug did not exhibit antibacterial activity. The zones of inhibition of compound G2 against Micrococcus luteus (36.2 +/- 1.0 mm) and Serratia marcescens (28.2 +/- 1.0 mm), and of compound G4 against Stenotrophomonas maltophilia (36.8 +/- 1.0 mm) were larger compared to the standard drug, doxycycline, exhibiting zones of inhibition 28.2 +/- 1.3, 28.2 +/- 0.9 and 20.0 +/- 0.9 mm, respectively. In addition, compounds G1 and G2 possessed significantly greater (p < 0.05) radical scavenging activity (82.3 +/- 1.8 and 92.3 +/- 2.2 %, respectively) than the precursor drug, gabapentin (63.2 +/- 2.6 %). The seizure scores for compounds GI (0.7 +/- 0.06) and G2 (0.9 +/- 0.07) were comparable (p > 0.05) with gabapentin (0.8 +/- 0.06), while compounds G3 and G4 were less active (p < 0.05) than gabapentin. Conclusion: Compounds G1 and G2 exhibit good antibacterial and antioxidant activities while retaining the anticonvulsant activity of the parent drug, gabapentin, thus making them suitable candidates for further development for the treatment of neurodegenerative pathologies associated with bacterial infections. About Benzophenone, If you have any questions, you can contact Saleem, MF; Khan, MA; Ahmad, I; Aslam, N; Khurshid, U or concate me.. Safety of Benzophenone

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Safety of Benzophenone. Authors Maslov, DK; Bukatov, GD in PLEIADES PUBLISHING INC published article about in [Maslov, D. K.; Bukatov, G. D.] Russian Acad Sci, Boreskov Inst Catalysis, Siberian Branch, Novosibirsk 630090, Russia in 2021.0, Cited 15.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

Titanium-magnesium catalysts (TMCs) of propylene polymerization have been synthesized in the presence of ketones as internal donors. The molar ratio of titanium chloride to ketone in TMCs was found to depend on the structure of ketone. The composition and catalytic properties of the synthesized TMCs in propylene polymerization were significantly different from those of TMCs prepared without ketone. The TMCs were synthesized by replacing ketones with a stereoregulating donor dibutyl phthalate (DBP, DBP/Mg = 0.05 mol/mol). It was shown that ketones were substituted by phthalate; the crystallite size of MgCl2 (similar to 6.5 nm in the 110 direction) did not change. The data on the molar ratio Ti/donor = 2 for different donors (ketone, phthalate) and the same MgCl2 crystallites are consistent with the predominance of 104 lateral cuts. The catalytic properties of the substituted catalysts are almost independent of the type of ketone used and are close to those of the standard TMC obtained with phthalate alone (DBP/Mg = 0.2 mol/mol) during the formation of MgCl2. Therefore, ketones, like esters, are involved in the formation of magnesium chloride. Their subsequent substitution by phthalate allows synthesis of TMCs with high activity and stereospecificity.

About Benzophenone, If you have any questions, you can contact Maslov, DK; Bukatov, GD or concate me.. Safety of Benzophenone

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Name: Benzophenone. Authors Wu, K; Ling, YC; Sun, N; Hu, BX; Shen, ZL; Jin, LQ; Hu, XQ in ROYAL SOC CHEMISTRY published article about in [Wu, Ke; Ling, Yichen; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Jin, Liqun; Hu, Xinquan] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310032, Peoples R China; [Jin, Liqun; Hu, Xinquan] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China in 2021.0, Cited 50.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

A nickel-catalyzed reductive decyanation of aromatic nitriles has been developed, in which the readily available and abundant ethanol was applied as the hydride donor. Various functional groups on the aromatic rings, such as alkoxyl, amino, imino and amide, were compatible in this catalytic protocol. Heteroaryl, benzylic and alkenyl nitriles were also tolerated. Mechanistic investigation indicated that ethanol provided hydride efficiently via beta-hydride elimination in this reductive decyanation.

About Benzophenone, If you have any questions, you can contact Wu, K; Ling, YC; Sun, N; Hu, BX; Shen, ZL; Jin, LQ; Hu, XQ or concate me.. Name: Benzophenone

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Category: thiomorpholine. Authors Hsu, KL in CELL PRESS published article about in [Hsu, Ku-Lung] Univ Virginia, Dept Chem, Charlottesville, VA 22904 USA; [Hsu, Ku-Lung] Univ Virginia, Sch Med, Dept Pharmacol, Charlottesville, VA 22908 USA; [Hsu, Ku-Lung] Univ Virginia, Dept Mol Physiol & Biol Phys, Charlottesville, VA 22908 USA; [Hsu, Ku-Lung] Univ Virginia, Ctr Canc, Charlottesville, VA 22903 USA in 2021.0, Cited 10.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

In this issue of Cell Chemical Biology, Seneviratne et al. (2020) combine photoaffinity labeling and quantitative chemical proteomics to identify the molecular target of a lead compound discovered from a phenotypic drug screen. Their work showcase the power of coupling a photoreactive group to screening hits for rapid target deconvolution.

About Benzophenone, If you have any questions, you can contact Hsu, KL or concate me.. Category: thiomorpholine

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

SDS of cas: 119-61-9. Authors Sahin, MO; Sanli, O in ELSEVIER published article about in [Sahin, Merve Olukman] Hatay Mustafa Kemal Univ, Res & Applicat Ctr Technol & Res & Dev, Tayfur Sokmen Campus, Antakya, Hatay, Turkey; [Sanli, Oya] Gazi Univ, Fac Sci, Dept Chem, Ankara, Turkey in 2021.0, Cited 29.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

In this study, in-situ synthesis of zinc oxide (ZnO) nanoparticles was utilized as an effective approach to prepare poly(vinyl alcohol) (PVA) and poly(vinyl alcohol)-graft-acrylonitrile/2-hydroxyethyl methacrylate (PVA-g-AN/HEMA) membranes with ZnO nanoparticles. The membranes were characterized by using Frourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), X-Ray diffraction (XRD) and contact angle measurements. Both of the membranes were utilized in separation of acetone/water mixtures via pervaporation technique and the optimum conditions regarding ZnO content within the membranes, acetone content in the feed solution and operating temperature were determined. PVA-g-AN/HEMA-ZnO nanocomposite membranes showed high permeation rate but low separation factor compared to PVA-ZnO nanocomposite membranes. Permeation rate and separation factor values were found to be in the range of 0.028-0.137 and 0.035-0.174 kg m(-2) h(-1), 17.61-325 and 9.4-84.5 depending on the pervaporation conditions for PVA-ZnO and PVA-g-AN/HEMA-ZnO nanocomposite membranes, respectively. (C) 2020 Elsevier B.V. All rights reserved.

SDS of cas: 119-61-9. About Benzophenone, If you have any questions, you can contact Sahin, MO; Sanli, O or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

In 2021.0 CHEM-EUR J published article about PRIMARY PHOSPHINES; CHEMISTRY; COMPLEXES; STABILITY; CRYSTAL; LIGANDS in [Horky, Filip; Cisarova, Ivana; Stepnicka, Petr] Charles Univ Prague, Dept Inorgan Chem, Fac Sci, Hlavova 2030, Prague 12840, Czech Republic in 2021.0, Cited 35.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9. HPLC of Formula: C13H10O

(Ferrocenylmethyl)phosphane (1) oxidation with hydrogen peroxide, elemental sulfur and grey selenium produced (ferrocenylmethyl)phosphane oxide 1O, sulfide 1S and selenide 1Se, respectively, as the first isolable primary phosphane chalcogenides lacking steric protection. At elevated temperatures, compound 1O disproportionated into 1 and (ferrocenylmethyl)phosphinic acid. In reactions with [(eta(6)-mes)RuCl2](2), 1O underwent tautomerization into a phosphane complex [(eta(6)-mes)RuCl2{FcCH(2)PH(OH)-kappa P}], whereas 1S and 1Se lost their P-bound chalcogen atoms, giving rise to the phosphane complex [(eta(6)-mes)RuCl2(FcCH(2)PH(2)-kappa P)] (Fc = ferrocenyl, mes= mesitylene). No tautomerization was observed in the reaction of 1O with B(C6F5)(3), which instead produced a Lewis pair FcCH(2)P(O)H-2-B(C6F5)(3). Phosphane oxide 1O added to C=O bonds of aldehydes and ketones and even to cumulenes PhNCE (E=O and S). However, both PH hydrogens were only employed in the reactions with aldehydes and cyanates.

About Benzophenone, If you have any questions, you can contact Horky, F; Cisarova, I; Stepnicka, P or concate me.. HPLC of Formula: C13H10O

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Quality Control of Benzophenone. I found the field of Science & Technology – Other Topics very interesting. Saw the article Ahmed implant coated with poly(2-methacryloyloxyethyl phosphorylcholine) inhibits foreign body reactions in rabbit eyes published in 2021.0, Reprint Addresses Kee, C (corresponding author), Sungkyunkwan Univ, Dept Ophthalmol, Samsung Med Ctr, Sch Med, Seoul, South Korea.. The CAS is 119-61-9. Through research, I have a further understanding and discovery of Benzophenone.

Purpose Wound healing after Ahmed glaucoma valve (AGV) implantation often entails fibrosis as a foreign body reaction to the silicone plate. Poly(2-methacryloyloxyethyl phosphorylcholine) (PMPC) forms an antifouling surface that inhibits fibrosis during wound healing. In this study, we aimed to compare the effects of the implantation of AGV coated with PMPC (wPMPC) versus AGV without PMPC (woPMPC) in rabbits. Methods Six New Zealand White rabbit does underwent AGV implantation in both eyes. For each rabbit, one eye was randomly selected for implantation of AGV wPMPC and a conventional AGV (woPMPC) was implanted in the contralateral eye. Gross conjunctival vascularity was compared between the two groups at the first, second, and fourth weeks after surgery. The eyes were enucleated in four weeks and subjected to staining with hematoxylin and eosin and Masson’s trichrome stain. The fibrosis and inflammation status among the eye samples were compared by measuring the thickness of the fibrotic walls and counting the number of chronic inflammatory cells around the AGV. Counting of inflammatory cells and measuring fibrotic wall thickness were done in a blinded method to eliminate observer bias. Statistical analysis was performed using the Mann-Whitney U test. Results Gross and histological examinations revealed no toxic effects of PMPC. There were no apparent differences in overall conjunctival vascularity between the two groups at weeks 1, 2, and 4 after surgery. The average inflammatory cell counts were 14.3 5.8 per slide and 27.3 +/- 8.6 per slide in the wPMPC and woPMPC groups, respectively (p = 0.037). The average thicknesses of the fibrotic wall were 57.9 +/- 11.3 mu m and 81.5 +/- 21.3 mu m in the wPMPC and woPMPC groups, respectively (p = 0.025). Conclusion Compared to the woPMPC group, the number of inflammatory cells and fibrosis were significantly decreased in the wPMPC group.

Quality Control of Benzophenone. About Benzophenone, If you have any questions, you can contact Kee, HJ; Lee, EJ; Han, JC; Kee, C or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

I found the field of Environmental Sciences & Ecology very interesting. Saw the article Free available chlorine initiated Baeyer-Villiger oxidation: A key mechanism for chloroform formation during aqueous chlorination of benzophenone UV filters published in 2021. Safety of Benzophenone, Reprint Addresses Wei, DB (corresponding author), Chinese Acad Sci, Res Ctr Ecoenvironm Sci, 18 Shuangqing Rd, Beijing 100085, Peoples R China.. The CAS is 119-61-9. Through research, I have a further understanding and discovery of Benzophenone

Chloroform, a regulated disinfection by-product in water, is often generated during chlorination disinfection treatment. However, the formation of chloroform is heavily dependent on the molecular structures of precursors. Moreover, compounds containing ketone moiety are ubiquitous in water environments. However, it is unclear if they can generate chloroform during chlorination. In this study, 14 benzophenones (BPs), efficient and widely used UV filters, with different substituents were selected to explore chloroform formation during chlorination. All 14 BPs generated chloroform, with yields dependent on their molecular structures and operational conditions. Compounds 2,2′,4,4′-tetrahydroxy-BP and benzophenone produced the highest and lowest chloroform of 0.313 and 0.013 g/g, respectively, corresponding to the fastest and slowest formation rate constants of 1.41 x 10(-1) and 2.71 x 10(-2) min(-1). Alkaline conditions and high chlorine dosages were favorable to chloroform formation. Three reactions played key roles in chloroform formation from BPs: (1) chlorine initiated Baeyer Villiger oxidation converted ketone moieties of BP molecules into esters; (2) the esters further underwent hydrolysis and formed phenolic and benzoic products; and (3) benzoic acids underwent decarboxylation and hydrolysis to form phenolic products. Subsequently, these phenolic products could further generate chloroform in the chlorination system. More importantly, BPs could generate chloroform in the ambient water matrices during practical chlorination treatment. This work emphasized the critical role of Baeyer-Villiger oxidation for chloroform formation, implying that pollutants containing aromatic ketone moieties generate chloroform during chlorination disinfection, and their potential risk should therefore be reviewed. (C) 2020 Elsevier Ltd. All rights reserved.

About Benzophenone, If you have any questions, you can contact Zhang, XY; Wei, DB; Sun, XF; Bai, CZ; Du, YG or concate me.. Safety of Benzophenone

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Will, C; Huelsmann, RD; Mafra, G; Merib, J; Anderson, JL; Carasek, E in [Will, Camila; Huelsmann, Ricardo Dagnoni; Mafra, Gabriela; Carasek, Eduardo] Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil; [Carasek, Eduardo] Univ Fed Ciencias Saude Porto Alegre, Dept Farmacociencias, BR-90050170 Porto Alegre, RS, Brazil; [Anderson, Jared L.] Iowa State Univ, Dept Chem, Ames, IA 50011 USA published High-throughput approach for the in situ generation of magnetic ionic liquids in parallel-dispersive droplet extraction of organic micropollutants in aqueous environmental samples in 2021.0, Cited 38.0. Category: thiomorpholine. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9.

In this work, a novel and high-throughput parallel-dispersive droplet extraction (Pa-DDE) based on in situ formation of the hydrophobic MILs ([Co(C4IM)(4)(+2)]2[NTf2-], [Ni(C4IM)(4)(+2)]2[NTf2-] and [Ni(BeIM)(4)(+2)]2[NTf2]) is demonstrated, for the first time, for the determination of benzophenone, metolachlor, triclocarban, pendimethalin, 4-methylbenzylidene camphor, and 2-ethylhexyl-4-methoxycinnamate from aqueous environmental samples. This experimental setup is comprised of a 96-well plate system containing a set of magnetic pins which were used to collect the MIL droplet after in situ formation. This consolidated system enabled simultaneous extraction of up to 96 samples and MIL production in one step. Using this apparatus, sample preparation times of 0.78 min per sample was achieved. The experimental conditions were carefully optimized using uni and multivariate approaches. The optimal conditions were comprised of sample volume of 1.25 mL, 4 mg of [Co (C4IM)(4)(+2)]2[Cl] and 40 mu L of LiNTf2 for the in situ formation, and dilution in 20 mu L of acetonitrile. The analytical parameters of merit were successfully determined with LODs ranging from 7.5 to 25 mu g L-1 and coefficients of determination higher than 0.989. Intraday and interday precision ranged from 6.4 to 20.6% (n = 3) and 11.6-22.9% (n = 9), respectively, with analyte relative recovery ranging between 53.9 and 129.1%.

Category: thiomorpholine. About Benzophenone, If you have any questions, you can contact Will, C; Huelsmann, RD; Mafra, G; Merib, J; Anderson, JL; Carasek, E or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Safety of Benzophenone. Authors Dmitrienko, A; Pilkington, M; Nikonov, GI in WILEY-V C H VERLAG GMBH published article about in [Dmitrienko, Anton; Pilkington, Melanie; Nikonov, Georgii I.] Brock Univ, Dept Chem, 1812 Sir Isaac Brock Way, St Catharines, ON L2S 3A1, Canada in 2021.0, Cited 22.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

The Al-I compound NacNacAl (1, NacNac = [ArNC(Me)CHC(Me)NAr](-), Ar = 2,6-iPr(2)C(6)H(3)) serves as a template for the chemoselective coupling between carbonyls (benzophenone, fenchone, isophorone, p-tolyl benzoate, N,N-dimethylbenzamide, (1-phenylethylidene)aniline) and pyridine. With the CH-acidic ketone (1R)-(+) camphor, the reaction affords a hydrido alkoxide compound of Al, formed as the result of enolization, whereas an enolizable imine, (1-phenylethylidene)aniline, and the bulky ketone isophorone, still chemoselectively couple with pyridine. In contrast, reaction with the ester p-tolyl benzoate results in cleavage of the ester bond together with replacement of the alkoxy group by a hydrogen atom of the pyridine moiety. This study demonstrates that for carbonyl substrates featuring phenyl substituents, the reaction proceeds via intermediate formation of eta(2)(C,X)-coordinated (X = O, N) carbonyl adducts, whereas the reaction of 1 with (R)-(-)-fenchone in the absence of pyridine leads to CH activation in the pendant isopropyl group of the Ar substituent of the NacNac ligand.

Safety of Benzophenone. About Benzophenone, If you have any questions, you can contact Dmitrienko, A; Pilkington, M; Nikonov, GI or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem