Discovery of 2005-10-9

About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Luo, Z; Gao, ZH; Song, ZY; Han, YF; Ye, S or concate me.. Recommanded Product: 2005-10-9

Recently I am researching about 9-MESITYL-10-METHYLACRIDINIUM ION; OXYGENATION; CYCLIZATION; ACID; DIBENZOPYRANONES; BENZOPYRANONES; INSERTION; DRIVEN, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21425207, 21521002, 21702208]; Chinese Academy of SciencesChinese Academy of Sciences. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Luo, Z; Gao, ZH; Song, ZY; Han, YF; Ye, S. The CAS is 2005-10-9. Through research, I have a further understanding and discovery of 6H-Benzo[c]chromen-6-one. Recommanded Product: 2005-10-9

A visible light mediated oxidative lactonization of 2-methyl-1,1′-biaryls was developed, giving benzocoumarins in good yields. The reaction features multiple C-H functionalization processes with oxygen as the final oxidant. The corresponding 2-aldehdyes, alcohols and carboxylic acids of the 1,1′-biaryls also worked well for the reaction.

About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Luo, Z; Gao, ZH; Song, ZY; Han, YF; Ye, S or concate me.. Recommanded Product: 2005-10-9

Reference:
Article; Zhang, Jian; Shi, Dongdong; Zhang, Haifeng; Xu, Zheng; Bao, Hanyang; Jin, Hongwei; Liu, Yunkui; Tetrahedron; vol. 73; 2; (2017); p. 154 – 163;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Chemical Properties and Facts of 6H-Benzo[c]chromen-6-one

About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Wang, JY; Peng, T; Zhang, XY; Xie, SL; Zheng, PM; Yao, K; Ke, YB; Wang, ZH; Jiang, HY or concate me.. Application In Synthesis of 6H-Benzo[c]chromen-6-one

Recently I am researching about BROAD-SPECIFICITY; MONOCLONAL-ANTIBODY; ORGANOPHOSPHORUS PESTICIDES; MONOMETHYL ETHER; HAPTEN DESIGN; IMMUNOASSAY; RECOGNITION; SELECTIVITY; OFLOXACIN; ELISA, Saw an article supported by the Ministry of Science and Technology of the People’s Republic of ChinaMinistry of Science and Technology, China [2017YFF0211003]; Sanming Project of Medicine in Shenzhen [SZSM201611068]. Published in WILEY in HOBOKEN ,Authors: Wang, JY; Peng, T; Zhang, XY; Xie, SL; Zheng, PM; Yao, K; Ke, YB; Wang, ZH; Jiang, HY. The CAS is 2005-10-9. Through research, I have a further understanding and discovery of 6H-Benzo[c]chromen-6-one. Application In Synthesis of 6H-Benzo[c]chromen-6-one

The antigen-antibody interaction determines the sensitivity and specificity of competitive immunoassay for hapten detection. In this paper, the specificity of a monoclonal antibody against alternariol-like compounds was evaluated through indirect competitive ELISA. The results showed that the antibody had cross-reactivity with 33 compounds with the binding affinity (expressed by IC50) ranging from 9.4 ng/mL to 12.0 mu g/mL. All the 33 compounds contained a common moiety and similar substituents. To understand how this common moiety and substituents affected the recognition ability of the antibody, a three-dimensional quantitative structure-activity relationship (3D-QSAR) between the antibody and the 33 alternariol-like compounds was constructed using comparative molecular field analysis (CoMFA) and comparative molecular similarity indices analysis (CoMSIA) methods. The q(2) values of the CoMFA and CoMSIA models were 0.785 and 0.782, respectively, and the r(2) values were 0.911 and 0.988, respectively, indicating that the models had good predictive ability. The results of 3D-QSAR showed that the most important factor affecting antibody recognition was the hydrogen bond mainly formed by the hydroxyl group of alternariol, followed by the hydrophobic force mainly formed by the methyl group. This study provides a reference for the design of new hapten and the mechanisms for antibody recognition.

About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Wang, JY; Peng, T; Zhang, XY; Xie, SL; Zheng, PM; Yao, K; Ke, YB; Wang, ZH; Jiang, HY or concate me.. Application In Synthesis of 6H-Benzo[c]chromen-6-one

Reference:
Article; Zhang, Jian; Shi, Dongdong; Zhang, Haifeng; Xu, Zheng; Bao, Hanyang; Jin, Hongwei; Liu, Yunkui; Tetrahedron; vol. 73; 2; (2017); p. 154 – 163;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Final Thoughts on Chemistry for Dimethyl 5-aminoisophthalate

Application In Synthesis of Dimethyl 5-aminoisophthalate. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Pearce, KG; Crossley, IR or concate me.

Application In Synthesis of Dimethyl 5-aminoisophthalate. Recently I am researching about ONE-POT SYNTHESIS; P=C BONDS; PHOSPHORUS; CHEMISTRY; SEPARATION; MOLECULES; CAVITIES, Saw an article supported by the Royal SocietyRoyal Society of LondonEuropean Commission; University of Sussex. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Pearce, KG; Crossley, IR. The CAS is 99-27-4. Through research, I have a further understanding and discovery of Dimethyl 5-aminoisophthalate

The condensation of MeP(SiMe3)(2) with a series of 5-substituted isophthaloyl chlorides (5-R’C6H3-2,6-{C(O)Cl}(2)) affords the diphosphametacyclophanes m-{-C(O)-C6H3-5-R’-(C(O)PMe)}(2) (R’ = I, Me, tBu, Ph, and p-NCC6H4); the analogues m-{-C(O)-C5H3N-(C(O)PMe)}(2) and m-{-C(O)-C6H4-(C(O)PPh)}(2) are similarly obtained in preference to higher oligomers, in contrast to precedent reports. The cyclophanes all adopt butterfly-like conformations in the solid state with the P-organyl substituents adopting mutually exo arrangements. Structural and computational data suggest the nature of the 5-R substituent is key in directing the inter-ring angle and the extent of LUMO stabilization about the diketophophanyl scaffold. The latter is substantiated by UV/vis spectroscopy and cyclic voltammetry, which demonstrate these cyclophanes to be appreciably comparable to the diketophosphanyl systems commonly explored in the context of organic electronic materials; intriguingly, the distinct dikeophosphanyl moieties within the macrocycles appear effectively insulated by the macrocycle geometry, rather than acting as a through-conjugate.

Application In Synthesis of Dimethyl 5-aminoisophthalate. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Pearce, KG; Crossley, IR or concate me.

Reference:
Patent; ASTRA ZENECA AB; NPS PHARMACEUTICALS, INC.; WO2004/14881; (2004); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Brief introduction of Dimethyl 5-aminoisophthalate

Category: esters-buliding-blocks. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Wilson, BH; Kruger, PE or concate me.

Recently I am researching about METAL-ORGANIC FRAMEWORKS; CO2; SORPTION; CAPTURE, Saw an article supported by the MacDiarmid Institute; Roper Scholarship (UC); New Zealand-France Friendship Fund. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Wilson, BH; Kruger, PE. The CAS is 99-27-4. Through research, I have a further understanding and discovery of Dimethyl 5-aminoisophthalate. Category: esters-buliding-blocks

A family of four novel pyrazinyl-hydrazone based ligands have been synthesized with differing functionality at the 5-position of the central aromatic ring. Previous work has shown such ligands to form dinuclear triple mesocates which pack to form hexagonal channels capable of gas sorption. The effect of the peripheral functionality of the ligand on the crystal packing was investigated by synthesizing complexes1to4which feature amino, bromo, iodo and methoxy substituents respectively. Complexes1to3crystallized in the same hexagonal space groupP6(3)/mand featured 1D channels. However, on closer inspection while the packing of1is mediated by hydrogen bonding interactions, the packing of complexes2and3are not, due to a subtlety different pi-pi stacking interaction enforced by the halogen substituent. The more bulky nature of the methoxy substituent of4results in the complex crystallizing in the triclinic space groupP-1, featuring an entirely different crystal packing.

Category: esters-buliding-blocks. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Wilson, BH; Kruger, PE or concate me.

Reference:
Patent; ASTRA ZENECA AB; NPS PHARMACEUTICALS, INC.; WO2004/14881; (2004); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Some scientific research about 99-27-4

Quality Control of Dimethyl 5-aminoisophthalate. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Derasp, JS; Beauchemin, AM or concate me.

Derasp, JS; Beauchemin, AM in [Derasp, Joshua S.; Beauchemin, Andre M.] Univ Ottawa, Dept Chem & Biomol Sci, Ctr Catalysis Res & Innovat, Ottawa, ON K1N 6N5, Canada published Rhodium-Catalyzed Synthesis of Amides from Functionalized Blocked Isocyanates in 2019, Cited 80. Quality Control of Dimethyl 5-aminoisophthalate. The Name is Dimethyl 5-aminoisophthalate. Through research, I have a further understanding and discovery of 99-27-4.

Isocyanates are useful building blocks for the synthesis of amides, although their widespread use has been limited by their high reactivity, which often results in poor functional group tolerance and a propensity to oligomerize. Herein, a rhodium-catalyzed synthesis of amides is described coupling boroxines with blocked (masked) isocyanates. The success of the reaction hinges on the ability to form both the isocyanate and the organorhodium intermediates in situ. Relying on masked isocyanate precursors and on the high reactivity of the organorhodium intermediate results in broad functional group tolerance, including protic nucleophilic groups such as amines, anilines, and alcohols.

Quality Control of Dimethyl 5-aminoisophthalate. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Derasp, JS; Beauchemin, AM or concate me.

Reference:
Patent; ASTRA ZENECA AB; NPS PHARMACEUTICALS, INC.; WO2004/14881; (2004); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Why Are Children Getting Addicted To C10H11NO4

About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Xiang, XL; Liu, YY; Liu, Y; Wang, XY; Jin, YG or concate me.. Safety of Dimethyl 5-aminoisophthalate

Recently I am researching about CHEMICAL-COMPOSITION; PHYSICAL-PROPERTIES; DUCK EGG; BIO-OIL; MICROSTRUCTURE; MEAT; SPECTROSCOPY; TEMPERATURE; EXTRACTION; VOLATILES, Saw an article supported by the Special Fund for the Modern Agro-Industry Technology Research System [CARS-40-K24]. Published in ELSEVIER SCI LTD in OXFORD ,Authors: Xiang, XL; Liu, YY; Liu, Y; Wang, XY; Jin, YG. The CAS is 99-27-4. Through research, I have a further understanding and discovery of Dimethyl 5-aminoisophthalate. Safety of Dimethyl 5-aminoisophthalate

Lipid migration is widespread in food system and has an important effect on food quality. It is urgent to explore the lipid migration in egg yolk after heating. The content of lipids in upper part (HL) was higher than that in bottom part (LL), and the lipids migration in yolk gel under heating were confirmed by MRI (T1) and T2 relaxation time of LF-NMR. Subsequently, the XDR result demonstrated the high lipid content induced the decrease in crystallinity of protein in HL part. The structures of HL part trend to be more ordered, stable (beta-sheet & beta-turns) and flat (alpha-helices) than LL part, also, more water distributed in LL part were observed by FTIR spectrum. The SEM results revealed that lipids migrated from LL to HL part, eventually lead to the protein in HL part of heated yolk gel unfold, the globular structure collapsed and become flatter. Morever, ethyl acetate, hexanal, etc. and hexanal, ethyl acetate, dimethyl-silanediol, etc. were identified as the main VOCs of LL and HL part of heated yolk gel, respectively. Lipid migration result in more lipid-specific volatiles were formed in the HL part, such as hexanal, 3-hydroxy-cyclohexanone, 2-pentyl-furan, D-limonene, 2-ethyl-1-hexanol, benzeneacetaldehyde. Lipid migration in heated yolk gel, caused by heat treatment, resulted in the changes of structure and flavor between HL and LL part.

About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Xiang, XL; Liu, YY; Liu, Y; Wang, XY; Jin, YG or concate me.. Safety of Dimethyl 5-aminoisophthalate

Reference:
Patent; ASTRA ZENECA AB; NPS PHARMACEUTICALS, INC.; WO2004/14881; (2004); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An update on the compound challenge: 103-26-4

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Alletto, F; Adamo, MFA or concate me.. SDS of cas: 103-26-4

An article Enantiospecific on-water bromination: a mild and efficient protocol for the preparation of alkyl bromides WOS:000598242900013 published article about SUBSTITUTION; REACTIVITY in [Alletto, Francesco; Adamo, Mauro F. A.] Royal Coll Surgeons Ireland, Dept Chem, Ctr Synth & Chem Biol CSCB, 123 St Stephens Green, Dublin 2, Ireland in 2020.0, Cited 23.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. SDS of cas: 103-26-4

Herein we report the first example of an on-water enantiospecific synthesis of alkyl bromides. This procedure allowed the conversion of secondary activated alkyl sulphides to benzylic alkyl bromides, which were obtained in 80-99% yields. The reaction carried out on enantio-pure sulphides provided the corresponding bromides in high yields and enantioselectivity (up to 92% ee; 94% es) at room temperature. The on-water conditions reduced significantly the reaction times compared to similar procedures run in organic media. The condition identified made use of no solvent, required no temperature control and produced a smooth organic phase easily separated for further synthetic use on a multigram-scale without the need for any organic extraction. Therefore, the present constitutes the most operationally simple and environmentally benign approach to a class of much sought organic intermediates.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Alletto, F; Adamo, MFA or concate me.. SDS of cas: 103-26-4

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

The Absolute Best Science Experiment for 6H-Benzo[c]chromen-6-one

Product Details of 2005-10-9. About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Cheng, KY; Cai, ZQ; Fu, J; Sun, XB; Sun, WL; Chen, L; Zhang, DD; Liu, W or concate me.

In 2019.0 CHEM ENG J published article about HEAVY-METAL IONS; DEPOSITED TITANATE NANOTUBES; ZERO-VALENT IRON; WASTE-WATER; TITANIUM-DIOXIDE; SIMULTANEOUS REMOVAL; AQUEOUS-SOLUTIONS; TIO2; OXIDATION; MONTMORILLONITE in [Cheng, Kaiyu] Zhejiang Univ, Ocean Coll, Zhoushan 316021, Peoples R China; [Cai, Zhengqing; Sun, Xianbo] East China Univ Sci & Technol, Natl Engn Lab High Concentrat Refractory Organ Wa, Shanghai 200237, Peoples R China; [Cai, Zhengqing; Fu, Jie] Fudan Univ, Dept Environm Sci & Engn, Shanghai 200433, Peoples R China; [Sun, Weiliang] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China; [Chen, Long; Zhang, Dandan; Liu, Wen] Peking Univ, Key Lab Water & Sediment Sci, Minist Educ, Coll Environm Sci & Engn, Beijing 100871, Peoples R China in 2019.0, Cited 66.0. The Name is 6H-Benzo[c]chromen-6-one. Through research, I have a further understanding and discovery of 2005-10-9. Product Details of 2005-10-9

Combined water pollution with the coexistence of heavy metals and organic contaminants is of great concern for practical wastewater treatment. In this study, a jaboticaba-like nanocomposite, titanate nanotubes supported TiO2 (TiO2/TiNTs), was synthesized by a two-step hydrothermal treatment. TiO2 /TiNTs had large surface area, abundant of -ONa/H groups and fine crystal anatase phase, thus exhibited both good adsorptive performance for Cu(II) and high photocatalytic activity for phenanthrene degradation. The maximum Cu(II) adsorption capacity on TiO2/TiNTs was 115.0 mg/g at pH 5 according to Langmuir isotherm model, and > 95% of phenanthrene was degraded within 4 h under UV light. TiO2/TiNTs showed about 10 times higher observed rate constant (k(obs) ) for phenanthrene degradation compared to the unmodified TiNTs. More importantly, the coexistence of Cu(II) promoted photocatalytic degradation of phenanthrene, because the incorporated Cu(II) in the lattice of TiNTs could trap photo-excited electron and thus inhibited the electron-hole recombination. Density functional theory (DFT) calculation indicated that the sites of phenanthrene with high Fukui index (f(0)) preferred to be attacked by center dot OH radicals. The quantitative structure-activity relationship (QSAR) analysis revealed that the degradation intermediates had lower acute toxicity and mutagenicity than phenanthrene. TiO2/TiNTs also owned high stability, as only slight loss of Cu(II) and phenanthrene removal efficiency was observed even after four reuse cycles. The developed material in this study is of great application potential for water or wastewater treatment with multi-contaminants, and this work can help us to better understand the mechanisms on reaction between Ti-based nanomaterials and different kinds of contaminants.

Product Details of 2005-10-9. About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Cheng, KY; Cai, ZQ; Fu, J; Sun, XB; Sun, WL; Chen, L; Zhang, DD; Liu, W or concate me.

Reference:
Article; Zhang, Jian; Shi, Dongdong; Zhang, Haifeng; Xu, Zheng; Bao, Hanyang; Jin, Hongwei; Liu, Yunkui; Tetrahedron; vol. 73; 2; (2017); p. 154 – 163;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Discover the magic of the C10H11NO4

About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Zhou, DD; Zhang, HC; Ma, CH; Han, HJ; Xie, MR or concate me.. Computed Properties of C10H11NO4

Recently I am researching about POLYNORBORNENE DERIVATIVES; POLYMER NANOCOMPOSITES; STRONGLY DIPOLAR; CONSTANT; DENSITY; METATHESIS; CYCLOPOLYMERIZATION; BREAKDOWN; POLYTHIOUREA; CATALYST, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21574041, 21704025]. Computed Properties of C10H11NO4. Published in ELSEVIER SCIENCE BV in AMSTERDAM ,Authors: Zhou, DD; Zhang, HC; Ma, CH; Han, HJ; Xie, MR. The CAS is 99-27-4. Through research, I have a further understanding and discovery of Dimethyl 5-aminoisophthalate

Disubstituted pendant-functionalized block copolymer consisting of insulating polynorbornene and conductive polyacetylene segments was synthesized by tandem metathesis polymerization, and displayed high dielectric constant of 30 and low dielectric loss of about 0.04, while behaved bad film-forming property, which could be improved by incorporating polycyclooctene into polynorbomene backbone. The generated flexible block copolymer with well-defined nanostructure exhibited a relatively high dielectric constant of 23, very low dielectric loss of below 0.0035, and high stored and released energy densities up to 4.52 and 4.02 J cm(-3) at the electric field of 165 MV m(-1),respectively, accompanied with the charge-discharge efficiency of 90%. The enhanced dielectric and energy storage capability were attributed to high permanent dipole moment and the interfacial polarization derived from the unique nanomorphology of block copolymer.

About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Zhou, DD; Zhang, HC; Ma, CH; Han, HJ; Xie, MR or concate me.. Computed Properties of C10H11NO4

Reference:
Patent; ASTRA ZENECA AB; NPS PHARMACEUTICALS, INC.; WO2004/14881; (2004); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Get Up to Speed Quickly on Emerging Topics:2005-10-9

Name: 6H-Benzo[c]chromen-6-one. About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Cheng, KY; Cai, ZQ; Fu, J; Sun, XB; Sun, WL; Chen, L; Zhang, DD; Liu, W or concate me.

An article Synergistic adsorption of Cu(II) and photocatalytic degradation of phenanthrene by a jaboticaba-like TiO2/titanate nanotube composite: An experimental and theoretical study WOS:000450105700109 published article about HEAVY-METAL IONS; DEPOSITED TITANATE NANOTUBES; ZERO-VALENT IRON; WASTE-WATER; TITANIUM-DIOXIDE; SIMULTANEOUS REMOVAL; AQUEOUS-SOLUTIONS; TIO2; OXIDATION; MONTMORILLONITE in [Cheng, Kaiyu] Zhejiang Univ, Ocean Coll, Zhoushan 316021, Peoples R China; [Cai, Zhengqing; Sun, Xianbo] East China Univ Sci & Technol, Natl Engn Lab High Concentrat Refractory Organ Wa, Shanghai 200237, Peoples R China; [Cai, Zhengqing; Fu, Jie] Fudan Univ, Dept Environm Sci & Engn, Shanghai 200433, Peoples R China; [Sun, Weiliang] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China; [Chen, Long; Zhang, Dandan; Liu, Wen] Peking Univ, Key Lab Water & Sediment Sci, Minist Educ, Coll Environm Sci & Engn, Beijing 100871, Peoples R China in 2019.0, Cited 66.0. The Name is 6H-Benzo[c]chromen-6-one. Through research, I have a further understanding and discovery of 2005-10-9. Name: 6H-Benzo[c]chromen-6-one

Combined water pollution with the coexistence of heavy metals and organic contaminants is of great concern for practical wastewater treatment. In this study, a jaboticaba-like nanocomposite, titanate nanotubes supported TiO2 (TiO2/TiNTs), was synthesized by a two-step hydrothermal treatment. TiO2 /TiNTs had large surface area, abundant of -ONa/H groups and fine crystal anatase phase, thus exhibited both good adsorptive performance for Cu(II) and high photocatalytic activity for phenanthrene degradation. The maximum Cu(II) adsorption capacity on TiO2/TiNTs was 115.0 mg/g at pH 5 according to Langmuir isotherm model, and > 95% of phenanthrene was degraded within 4 h under UV light. TiO2/TiNTs showed about 10 times higher observed rate constant (k(obs) ) for phenanthrene degradation compared to the unmodified TiNTs. More importantly, the coexistence of Cu(II) promoted photocatalytic degradation of phenanthrene, because the incorporated Cu(II) in the lattice of TiNTs could trap photo-excited electron and thus inhibited the electron-hole recombination. Density functional theory (DFT) calculation indicated that the sites of phenanthrene with high Fukui index (f(0)) preferred to be attacked by center dot OH radicals. The quantitative structure-activity relationship (QSAR) analysis revealed that the degradation intermediates had lower acute toxicity and mutagenicity than phenanthrene. TiO2/TiNTs also owned high stability, as only slight loss of Cu(II) and phenanthrene removal efficiency was observed even after four reuse cycles. The developed material in this study is of great application potential for water or wastewater treatment with multi-contaminants, and this work can help us to better understand the mechanisms on reaction between Ti-based nanomaterials and different kinds of contaminants.

Name: 6H-Benzo[c]chromen-6-one. About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Cheng, KY; Cai, ZQ; Fu, J; Sun, XB; Sun, WL; Chen, L; Zhang, DD; Liu, W or concate me.

Reference:
Article; Zhang, Jian; Shi, Dongdong; Zhang, Haifeng; Xu, Zheng; Bao, Hanyang; Jin, Hongwei; Liu, Yunkui; Tetrahedron; vol. 73; 2; (2017); p. 154 – 163;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics