Category: 119-61-9

Authors Suwannarat, S; Amnuaypanich, S; Chanlek, N; Amnuaypanich, S in ELSEVIER published article about in [Suwannarat, Siriwimol; Amnuaypanich, Sittipong] Khon Kaen Univ, Appl Chem Div, Dept Chem, Khon Kaen 40002, Thailand; [Suwannarat, Siriwimol; Amnuaypanich, Sittipong] Khon Kaen Univ, Appl Chem Div, Ctr Excellence Innovat Chem PERCH CIC, Fac Sci, Khon Kaen 40002, Thailand; [Suwannarat, Siriwimol; Amnuaypanich, Sujitra; Amnuaypanich, Sittipong] Khon Kaen Univ, Mat Chem Res Ctr MCRC KKU, Fac Sci, Khon Kaen 40002, Thailand; [Chanlek, Narong] Synchrotron Light Res Inst, 111 Univ Ave, Nakhon Ratchasima 30000, Thailand in 2021.0, Cited 35.0. Recommanded Product: 119-61-9. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

Temperature-enhanced water selectivity of MMMs was demonstrated for the dehydration pervaporation of ethanol solutions. The MMMs synthesized from Polyvinyl alcohol embedded with Poly(2-hydroxyethylmethacrylate)-grafted mesoporous silica nanoparticles revealed a concomitant increasing of the water selectivity and the water flux upon raising feed solution temperature from 30 degrees C to 60 degrees C. This phenomenon is rarely observed in PVA-based MMMs in which the water selectivity usually declines with increasing feed temperature. Remarkably, the temperature enhancing effect was intensified with increasing amount of the grafted PHEMA on MSNs. The enhancement of the water selectivity stems from the superior water absorption selectivity to the water diffusion selectivity because the water absorption by the MMMs is endothermic which gives rise to the favorable absorption as raising feed solution temperature. The incorporation of MSNs-g-PHEMA resulted in improving of both flux and the water selectivity because the mesoporous structure of MSNs-g-PHEMA provides unrestricted and hydrophilic paths for the water permeation.

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Reference:
Thiomorpholine – Wikipedia,
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Application In Synthesis of Benzophenone. Belov, DS; Mathivathanan, L; Beazley, MJ; Martin, WB; Bukhryakov, KV in [Belov, Dmitry S.; Mathivathanan, Logesh; Bukhryakov, Konstantin V.] Florida Int Univ, Dept Chem & Biochem, 11200 SW 8th St, Miami, FL 33199 USA; [Beazley, Melanie J.] Univ Cent Florida, Dept Chem, 4111 Libra Dr, Orlando, FL 32816 USA; [Martin, William Blake] Case Western Reserve Univ, Dept Macromol Sci & Engn, 2100 Adelbert Rd, Cleveland, OH 44106 USA published Stereospecific Ring-Opening Metathesis Polymerization of Norbornene Catalyzed by Iron Complexes in 2021.0, Cited 71.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9.

Developing well-defined iron-based catalysts for olefin metathesis would be a breakthrough achievement in the field not only to replace existing catalysts by inexpensive metals but also to attain a new reactivity taking advantage of the unique electronic structure of the base metals. Here, we present a two-coordinate homoleptic iron complex, Fe(HMTO)(2) [HMTO=O-2,6-(2,4,6-Me3C6H2)(2)C6H3], that is capable of performing ring-opening metathesis polymerization of norbornene to produce highly stereoregular polynorbornene (99 % cis, syndiotactic). The use of heteroleptic Fe(HMTO)(RO) [RO=(CH3)(2)CF3CO, CH3(CF3)(2)CO, or Ph(CF3)(2)CO] prepared in situ significantly increases the polymerization rate while preserving selectivity. The resulting polymers were characterized by H-1 and C-13 NMR spectroscopy and gel-permeation chromatography.

Application In Synthesis of Benzophenone. About Benzophenone, If you have any questions, you can contact Belov, DS; Mathivathanan, L; Beazley, MJ; Martin, WB; Bukhryakov, KV or concate me.

Reference:
Thiomorpholine – Wikipedia,
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Recommanded Product: 119-61-9. Authors Deshpande, NU; Virmani, M; Jayakannan, M in ROYAL SOC CHEMISTRY published article about in [Deshpande, Nilesh Umakant; Virmani, Mishika; Jayakannan, Manickam] Indian Inst Sci Educ & Res IISER Pune, Dept Chem, Dr Homi Bhabha Rd, Pune 411008, Maharashtra, India in 2021.0, Cited 55.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

We report aggregation induced emission (AIE) driven polysaccharide polymersomes as fluorescence resonance energy transfer (FRET) nanoprobes to study their intracellular enzyme-responsive delivery by real-time live-cell confocal microscopy bio-imaging techniques. An AIE active tetraphenylethylene (TPE) optical chromophore and plant-based vesicular directing hydrophobic unit were grafted on clinically relevant polysaccharide-dextran via enzyme-cleavable aliphatic ester chemical linkages. The TPE-tagged dextran self-assembled as 180 +/- 20 nm blue-luminescent polymersomes in aqueous medium and exhibited excellent encapsulation capabilities for water soluble Rose Bengal (RB) and water insoluble Nile red (NR) fluorophores. The selective photoexcitation of the TPE chromophore enabled the FRET process between the TPE donor and RB (or NR) acceptor molecule in <50 angstrom Forster distance afforded by the polymersome. The FRET probe was very stable under extracellular conditions and it exclusively underwent lysosomal esterase enzymatic biodegradation at the intracellular compartments to release RB. The enzyme-trigger enabled the FRET probe to function as an extracellular turn-ON -> intracellular turn-Off red-fluorescent signal (Probe-1). In this process, the AIE self-emission was also simultaneously restored on the TPE chromophore (blue-luminescent, Probe-2) followed by the isolation of donor and acceptor in the cytosol. As a result, this new design enabled the visualization of real-time enzyme-responsive delivery by monitoring the dual fluorescent signals from both the polymer host (blue) and encapsulated guest (red) in a single nano-platform. In vitro cytotoxicity studies established that the polymersome probe was non-toxic to cells up to 300 mu g mL(-1). Lyso-tracker staining experiments supported the FRET probe internalization in the lysosomal compartments for enzymatic-biodegradation. Live cell confocal microscopy with selective photo-excitation was used to directly monitor the enzyme-responsive FRET action in human breast cancer MCF 7 and wild-type mouse embryonic fibroblast cell lines (WT-MEFs). It was found that the tailor-made polymersome FRET probe was efficient to deliver the loaded cargo in <3 h in live cells which predicts the usefulness of the probe in biomedical research. About Benzophenone, If you have any questions, you can contact Deshpande, NU; Virmani, M; Jayakannan, M or concate me.. Recommanded Product: 119-61-9

Reference:
Thiomorpholine – Wikipedia,
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An article Research on VOCs and odor from heartwood and sapwood of paper mulberry (Broussonetia papyrifera (L.) Vent.) with different moisture content WOS:000657204500001 published article about VOLATILE ORGANIC-COMPOUNDS; AIR-QUALITY; EMISSIONS; PARTICLEBOARDS; OLFACTOMETRY; REMOVAL; LACQUER in [Wang, Qifan; Shen, Jun; Zeng, Bin; Wang, Huiyu] Northeast Forestry Univ, Coll Mat Sci & Engn, Main Res Direct Wood Sci & Technol, 26 Hexing Rd, Harbin 150040, Peoples R China in 2021.0, Cited 47.0. HPLC of Formula: C13H10O. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

The impact of volatile organic compounds (VOCs) and odor on indoor environment and people has attracted much attention. To reduce this problem of odorous compounds contained in wood panel, this study focused on identifying odorant compounds and exploring the influence of moisture content factors on VOCs and odor emissions. Paper mulberry (Broussonetia papyrifera (L.)Vent.) was investigated using the technology of gas chromatography-mass spectrometry/olfactory (GC-MS/O). Total volatile organic compounds (TVOC) and characteristic odor-active compounds were studied, and the emission of heartwood and sapwood of paper mulberry was compared at the same time. It was found that the main components from heartwood and sapwood were aromatics, alkanes, alkenes, aldehydes ketones, alcohols and esters. Totally, 23 kinds of odor-active compounds were identified from heartwood and sapwood of paper mulberry, among which, aromatics and aldehydes ketones were the main odorant compounds. Seven kinds of key odorant compounds were identified in this process. With the decrease in moisture content, the TVOC and total odor intensity of heartwood and sapwood generally decreased. The moisture content had a great effect on VOC release when the moisture content decreased from 70 to 50% and reduced from fiber saturation point (30%) to air saturation point (10%). The main odor impressions of paper mulberry were aromatic, fresh fruit fragrance, sweet scent and special pungent. In the whole process of moisture content decrease, the TVOC, concentration of odorant and odor intensity of sapwood were higher than that of heartwood.

HPLC of Formula: C13H10O. About Benzophenone, If you have any questions, you can contact Wang, QF; Shen, J; Zeng, B; Wang, HY or concate me.

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Thiomorpholine – Wikipedia,
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Category: thiomorpholine. In 2021.0 ORGANOMETALLICS published article about HETEROBIMETALLIC CARBENE COMPLEXES; NHC LIGANDS; IRIDIUM; ROUTE in [Nishad, Rajeev C.; Kumar, Shashi; Rit, Arnab] Indian Inst Technol Madras, Dept Chem, Chennai 600036, Tamil Nadu, India in 2021.0, Cited 47.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9.

A (bis)azolium salt [L1-H-2]Br-2 (5), synthesized following multistep procedures, was realized to be a suitable platform for accessing the bis(NHC) ligand supported heterobimetallic Ir-III-M (M = Pd-II/Au-I) complexes via a sequential metalation strategy for their potential catalytic applications in one-pot tandem organic transformations. First, the reaction of 5 with 0.5 equiv of [Ir(Cp*)Cl-2](2) selectively yielded a monometallic Ir-III complex 6, which was further metalated using Pd(OAc)(2)/NaOAc to afford the heterobimetallic Ir-III-Pd-II complex 7. On the other hand, complex 6 was reacted with Ag2O, followed by transmetalation with [Au(SMe2)Cl] in a one-pot manner, to yield the Ir-III-Au-I complex 8. Further, the related homobimetallic Ir-III and Pd-II complexes 9 and 10, respectively, have also been synthesized directly from [L1-H-2]Br-2. All the homo/heterobimetallic complexes have been well-characterized by multinuclear NMR spectroscopy, ESI-mass spectrometry, and via single-crystal X-ray diffraction studies of the complexes 7, 8, and 10. The heterobimetallic Ir-III-Pd-II complex 7 has been tested as a catalyst for three one-pot tandem catalytic reactions: (a) Suzuki-Miyaura coupling and transfer hydrogenation of ketones, (b) hydrodefluorination and transfer hydrogenation of ketones, and (c) hydrodehalogenation and transfer hydrogenation of imines. Importantly, the catalytic activity of heterobimetallic complex 7 in the above-mentioned reactions was found to be better than the mixture of their corresponding homobimetallic counterparts 9 and 10, keeping the concentration of the metal centers constant. These observations affirm some sort of cooperativity between the two metal centers (Ir and Pd) connected via a single ligand frame in 7 when catalytic activity is concerned, which thus constitutes a superior catalytic system than that of the cases where two separate metal complexes (hence, the two metal centers are not connected by a single ligand framework) are used.

Category: thiomorpholine. About Benzophenone, If you have any questions, you can contact Nishad, RC; Kumar, S; Rit, A or concate me.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Authors Xi, ZW; Yang, L; Wang, DY; Feng, CW; Qin, YF; Shen, YM; Pu, CD; Peng, XG in AMER CHEMICAL SOC published article about in [Xi, Zi-Wei; Wang, Dan-Yan; Feng, Chuan-Wei; Shen, Yong-Miao] Zhejiang Sci Tech Univ, Dept Chem, Key Lab Surface & Interface Sci Polymer Mat Zheji, Hangzhou 310018, Zhejiang, Peoples R China; [Yang, Lei; Peng, Xiaogang] Zhejiang Univ, Ctr Chem Novel & High Performance Mat, Dept Chem, Hangzhou 310027, Zhejiang, Peoples R China; [Qin, Yufeng; Pu, Chaodan] Shanghai Tech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China in 2021.0, Cited 133.0. Quality Control of Benzophenone. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

We present an efficient and versatile visible light-driven methodology to transform aryl aldehydes and ketones chemoselectively either to alcohols or to pinacol products with CdSe/CdS core/shell quantum dots as photocatalysts. Thiophenols were used as proton and hydrogen atom donors and as hole traps for the excited quantum dots (QDs) in these reactions. The two products can be switched from one to the other simply by changing the amount of thiophenol in the reaction system. The core/shell QD catalysts are highly efficient with a turn over number (TON) larger than 4 X 10(4) and 4 X 10(5) for the reduction to alcohol and pinacol formation, respectively, and are very stable so that they can be recycled for at least 10 times in the reactions without significant loss of catalytic activity. The additional advantages of this method include good functional group tolerance, mild reaction conditions, the allowance of selectively reducing aldehydes in the presence of ketones, and easiness for large scale reactions. Reaction mechanisms were studied by quenching experiments and a radical capture experiment, and the reasons for the switchover of the reaction pathways upon the change of reaction conditions are provided.

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

Computed Properties of C13H10O. In 2021.0 ADV SYNTH CATAL published article about PHOTOREDOX-CATALYZED SULFONYLATION; SULFUR-DIOXIDE; INSERTION; INHIBITORS; SULFONES in [Yao, Yanfang; Xie, Wenlin] Hunan Univ Sci & Technol, Sch Chem & Chem Engn, Xiangtan 411201, Peoples R China; [Yin, Ziqing; Chen, Weiyun; He, Fu-Sheng; Wu, Jie] Taizhou Univ, Sch Pharmaceut & Mat Engn, 1139 Shifu Ave, Taizhou 318000, Peoples R China; [Yin, Ziqing; Chen, Weiyun; He, Fu-Sheng; Wu, Jie] Taizhou Univ, Inst Adv Studies, 1139 Shifu Ave, Taizhou 318000, Peoples R China; [Wu, Jie] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China in 2021.0, Cited 60.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9.

A three-component reaction of aryldiazonium tetrafluoroborates, sodium metabisulfite, and 3-azido-2-methylbut-3-en-2-ol under mild conditions is described. By using abundant and cheap sodium metabisulfite as the sulfur dioxide surrogate, this protocol features good functional group compatibility, affording 2-arylsulfonylacetonitriles in moderate to good yields. The reaction proceeds smoothly at room temperature without the need of any catalysts or additives. Moreover, the synthetic utility of this method is demonstrated by the transformation of 2-arylsulfonylacetonitrile into 2-arylsulfonyl acetamide and 2-arylsulfonylethylamine.

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

COA of Formula: C13H10O. Dai, X; Li, XY; Tang, SL; Peng, XH; Zheng, XG; Jiang, O in [Dai, Xuan; Li, Xingyan; Tang, Shuangling; Peng, Xinhua] Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China; [Zheng, Xuegen; Jiang, Ou] Sinopec Anqing Petrochem Co, Anqing 246000, Peoples R China published Efficient aerobic oxidation of ethylbenzene accelerated by cu species in hydrotalcite in 2021.0, Cited 35.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9.

The simply prepared CuMgAl hydrotalcite (CuMgAl-LDH) has been developed as an efficient catalyst for the aerobic oxidation of ethylbenzene to acetophenone in the presence of N-Hydroxyphthalimide (NHPI). Various alkyl arenes could be tolerated under the selected reaction conditions. The kinetic study showed that the oxidation of ethylbenzene is a first-order reaction over CuMgAl-LDH. The mechanism study indicated that CuMgAl-LDH could accelerate not only the conversion of ethylbenzene, but also the transformation of the alcohol intermediate to ketone. The positive effect of surface basicity of the catalyst on the reaction has been observed in the aerobic oxidation of the ethylbenzene.

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

Healthcare careers for chemists are once again largely based in laboratories, although increasingly there is opportunity to work at the point of care, helping with patient investigation. 119-61-9, Name is Benzophenone, molecular formurla is C13H10O. In a document, author is Saikia, Anil K., introducing its new discovery. Synthetic Route of 119-61-9.

A one-pot, metal-free procedure has been developed for the synthesis of 4-tosylthiomorpholine from N-tethered thioalkenols via bromination, cyclization and subsequent elimination reaction in good yields. The reaction is found to be highly regioselective.

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Reference:
Thiomorpholine – Wikipedia,
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You could be based in a university, combining chemical research with teaching; or in a public-sector research center, helping to ensure national healthcare provision keeps pace with new discoveries. In an article, author is Reddy, L. Srikanth, once mentioned the application of 119-61-9, Name is Benzophenone, molecular formula is C13H10O, molecular weight is 182.2179, MDL number is MFCD00003076, category is thiomorpholine. Now introduce a scientific discovery about this category, Application In Synthesis of Benzophenone.

Quinazoline nucleus is present in various compounds and it is responsible for diverse biological activities. The present work mainly focused on the Quinazolines with potential activities that are now in development. The objective of this research work is to synthesize various compounds containing Quinazoline moiety and their derivatives as well as characterising the compounds by spectral analysis and screening for antimicrobial and anticancer activities. The structures of synthesized compounds were confirmed by various spectroscopic methods such as IR, NMR and mass spectroscopy. The products were evaluated for their antimicrobial activity against several microbes. Some of the compounds exhibited potent anti-bacterial activity as well as anti-fungal activity. Among the Novel Quinazoline derivatives 8i, 8j, 8d shows Excellent Anti-microbial activity

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