Ishihara, Nami’s team published research in Journal of Toxicological Sciences in 47 | CAS: 191-07-1

Journal of Toxicological Sciences published new progress about 191-07-1. 191-07-1 belongs to catalysis-chemistry, auxiliary class Electronic Materials, name is Coronene, and the molecular formula is C24H12, SDS of cas: 191-07-1.

Ishihara, Nami published the artcileInvolvement of polycyclic aromatic hydrocarbons and endotoxin in macrophage expression of interleukin-33 induced by exposure to particulate matter, SDS of cas: 191-07-1, the publication is Journal of Toxicological Sciences (2022), 47(5), 201-210, database is CAplus.

Air pollutants are important factors that contribute to the development and/or exacerbation of allergic inflammation accompanied by asthma, but exptl. evidence still needs to be collected. Interleukin 33 (IL-33) is closely involved in the onset and progression of asthma. In this study, we examined the effects of particulate matter (PM) on IL-33 expression in macrophages. PM2.5 collected in Yokohama, Japan by the cyclone device significantly induced IL-33 expression in human THP-1 macrophages, and the induction was clearly suppressed by pretreatment with the aryl hydrocarbon receptor (AhR) antagonist CH-223191 or the Toll-like receptor 4 (TLR4) antagonist TAK-242. PM2.5-induced IL-33 expression was significantly attenuated in AhR-knockout or TLR4-mutated macrophages, suggesting an important role of polycyclic aromatic hydrocarbons (PAHs) and endotoxin in IL-33 stimulation. PM samples derived from tunnel dust slightly but significantly induced IL-33 expression, while road dust PM did not affect IL-33 expression. The PAH concentration in tunnel dust was higher than that in road dust. Tunnel dust or road dust PM contained less endotoxin than PM2.5 collected in Yokohama. These data suggest that the potency of IL-33 induction could depend on the concentration of PAHs as well as endotoxin in PMs. Caution regarding PAHs and endotoxin levels in air pollutants should be taken to prevent IL-33-induced allergic inflammation.

Journal of Toxicological Sciences published new progress about 191-07-1. 191-07-1 belongs to catalysis-chemistry, auxiliary class Electronic Materials, name is Coronene, and the molecular formula is C24H12, SDS of cas: 191-07-1.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Krupoder, S. A.’s team published research in Russian Journal of General Chemistry (Translation of Zhurnal Obshchei Khimii) in 70 | CAS: 1206-46-8

Russian Journal of General Chemistry (Translation of Zhurnal Obshchei Khimii) published new progress about 1206-46-8. 1206-46-8 belongs to catalysis-chemistry, auxiliary class Organic Silicones, name is Trimethyl(perfluorophenyl)silane, and the molecular formula is C9H9F5Si, Recommanded Product: Trimethyl(perfluorophenyl)silane.

Krupoder, S. A. published the artcileIntramolecular interactions in aromatic compounds: V. Electronic structure of polyfluoroaromatic silanes and related hydrocarbons, Recommanded Product: Trimethyl(perfluorophenyl)silane, the publication is Russian Journal of General Chemistry (Translation of Zhurnal Obshchei Khimii) (2000), 70(1), 101-110, database is CAplus.

The electronic structure of pentafluorophenyl-substituted silanes ArnSiMe4-n (Ar = C6H5, C6F5, 4-FC6H4, 2,3,5,6-F4C5N; n = 1; Ar = C6H5, C6F5, n = 2, 4) was studied by x-ray emission and He(I) photoelectron spectroscopy. The He(I) photoelectron spectra were measured and interpreted from MNDO calculations, anal. of the p-fluoro effect, and relative intensities. Substitution of C6F5 for C6H5 in aryltrimethyl- and diaryldimethylsilanes results in enhanced ¦Ð interaction between the aryl and SiMen groups (n = 2, 3) by higher ¦Ð levels and has almost no effect on the charge on the Si atom.

Russian Journal of General Chemistry (Translation of Zhurnal Obshchei Khimii) published new progress about 1206-46-8. 1206-46-8 belongs to catalysis-chemistry, auxiliary class Organic Silicones, name is Trimethyl(perfluorophenyl)silane, and the molecular formula is C9H9F5Si, Recommanded Product: Trimethyl(perfluorophenyl)silane.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Mrzewinski, Tadeusz’s team published research in Biuletyn Wojskowej Akademii Technicznej imienia Jaroslawa Dabrowskiego in 13 | CAS: 1821-27-8

Biuletyn Wojskowej Akademii Technicznej imienia Jaroslawa Dabrowskiego published new progress about 1821-27-8. 1821-27-8 belongs to catalysis-chemistry, auxiliary class Nitro Compound,Amine,Benzene, name is Bis(4-nitrophenyl)amine, and the molecular formula is C12H9N3O4, Safety of Bis(4-nitrophenyl)amine.

Mrzewinski, Tadeusz published the artcileReactions of nitrogen dioxide with diphenylamine, Safety of Bis(4-nitrophenyl)amine, the publication is Biuletyn Wojskowej Akademii Technicznej imienia Jaroslawa Dabrowskiego (1964), 13(138), 59-67, database is CAplus.

An amount of 4.78-6.66 g. dry gaseous NO2, either O-free or containing 0.66-0.75 mol O per mol, was passed into a solution of 10 g. Ph2NH in 130 mL. C6H6, either without catalyst or with 0.01 mg. N,N-diphenyl-N’-picrylhydrazide (I), or with Bz2O2. The mixture was refluxed 0.5-3.5 h. at 20 or 77¡ã. The mixture was refluxed 0.5-3.5 h. at 20 or 77¡ã. The products were separated by means of fractional crystallization from acetone and were identified by determination of the m.p., mol. weight, and N content and also polarog. as weil as spectrophotometrically. The following products and yields were obtained, without catalysts at 20¡ã: N-nitroso-4-nitrodiphenylamine (II) 0.28 g. and N-nitrosodiphenylamine (III) in trace amount; with O at 20¡ã: II 0.20 g., III in trace amount, and diphenyldihydrophenazine (IV) 0.02 g.; with O at 77¡ã: II 0.15 and 2,4-dinitrodiphenylamine (V) 0.06 g.; with O and I at 20¡ã: II 0.70, III 0.10, V 0.30, 4,4′-dinitrodiphenylamine (VI) 0.22, 4-nitrodiphenylamine (VII) 0.10, and N,N’-bis(2,4-dinitrophenyl)benzidine (VIII) 0.90 g.; with O and I at 77¡ã: II and VI in trace amounts and V 0.20 g.; with 0.01 g. Bz2O2 at 20¡ã: II 0.84, III 0.41, V 0.42, VI 0.34, and N,N’-bis(4-nitrophenyl)benzidine (IX) 0.09 g.; with O and 0.01 g. of Bz2O2 during 3.5 h.: II 0.80, V 0.57, VI 0.31, VIII 0.15, IX 0.13, and 2,4,4′-trinitrodiphenylamine (X) 0.20 g.; with O and 0.10 g. Bz2O2 during 0.5 h.: II 0.64, V 0.50, VI 0.27, VII 0.19, IX 0.18, and X 0.32 g. A free-radical mechanism of the reaction is suggested according to the equation: Ph2NH + NO2 ¡ú Ph2N¡¤ + HNO2. The catalysts are considered to initiate the formation of radicals.

Biuletyn Wojskowej Akademii Technicznej imienia Jaroslawa Dabrowskiego published new progress about 1821-27-8. 1821-27-8 belongs to catalysis-chemistry, auxiliary class Nitro Compound,Amine,Benzene, name is Bis(4-nitrophenyl)amine, and the molecular formula is C12H9N3O4, Safety of Bis(4-nitrophenyl)amine.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Fukata, Yukihiro’s team published research in Organic Letters in 16 | CAS: 22693-41-0

Organic Letters published new progress about 22693-41-0. 22693-41-0 belongs to catalysis-chemistry, auxiliary class Other Functionalization Reagent, name is 2,4,6-Triisopropylbenzenethiol, and the molecular formula is C15H24S, Recommanded Product: 2,4,6-Triisopropylbenzenethiol.

Fukata, Yukihiro published the artcileAsymmetric Isomerization of ¦Ø-Hydroxy-¦Á,¦Â-Unsaturated Thioesters into ¦Â-Mercaptolactones by a Bifunctional Aminothiourea Catalyst, Recommanded Product: 2,4,6-Triisopropylbenzenethiol, the publication is Organic Letters (2014), 16(8), 2184-2187, database is CAplus and MEDLINE.

We present a novel methodol. for the asym. synthesis of ¦Â-mercaptolactones via isomerization of ¦Ø-hydroxy-¦Á,¦Â-unsaturated thioesters by means of a bifunctional aminothiourea catalyst. The catalyst interacts with the substrate through the cooperative action of both a covalent bond at the amino group and noncovalent bonding at the thiourea group. The potential for an enantiodivergent synthesis could also be demonstrated by carrying out the reaction in a different solvent system.

Organic Letters published new progress about 22693-41-0. 22693-41-0 belongs to catalysis-chemistry, auxiliary class Other Functionalization Reagent, name is 2,4,6-Triisopropylbenzenethiol, and the molecular formula is C15H24S, Recommanded Product: 2,4,6-Triisopropylbenzenethiol.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Ohya, Yuki’s team published research in Pediatric Transplantation in 17 | CAS: 38260-01-4

Pediatric Transplantation published new progress about 38260-01-4. 38260-01-4 belongs to catalysis-chemistry, auxiliary class Chelating Agents, name is N1,N1′-(Ethane-1,2-diyl)bis(ethane-1,2-diamine) dihydrochloride, and the molecular formula is C6H20Cl2N4, Related Products of catalysis-chemistry.

Ohya, Yuki published the artcileRe-evaluation of the indications for liver transplantation in Wilson’s disease based on the outcomes of patients referred to a transplant center, Related Products of catalysis-chemistry, the publication is Pediatric Transplantation (2013), 17(4), 369-373, database is CAplus and MEDLINE.

The aim of this study was to re-evaluate the indications and timing of LT for WD. From 2000 to 2009, eight patients with WD who had been referred to our institution for LT were enrolled in this study. The mean patient age was 15.9 yr (range, 7-37 yr). Four patients could not receive LT, because there were no available donors. All four patients were treated with chelating agent medication. Three of them (two of two patients with fulminant WD and one of two with cirrhotic WD) who did not undergo LT are still alive and doing well with stable liver functional tests. Only one of the patients with cirrhotic WD who did not undergo LT died of hepatic failure. Even among the four patients who underwent LT, one with fulminant WD recovered from hepatic encephalopathy with apheresis therapy and chelating agent. He later required LT because of severe neutropenia from D-penicillamine. The other three patients who underwent LT recovered and have been doing well. Some of the patients with WD can recover and avoid LT with medical treatment. Even when WD has progressed liver cirrhosis and/or fulminant hepatic failure at the time of diagnosis, medical treatment should be tried before considering LT.

Pediatric Transplantation published new progress about 38260-01-4. 38260-01-4 belongs to catalysis-chemistry, auxiliary class Chelating Agents, name is N1,N1′-(Ethane-1,2-diyl)bis(ethane-1,2-diamine) dihydrochloride, and the molecular formula is C6H20Cl2N4, Related Products of catalysis-chemistry.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Hashimoto, Hideki’s team published research in Japanese Journal of Applied Physics, Part 1: Regular Papers, Short Notes & Review Papers in 36 | CAS: 201157-13-3

Japanese Journal of Applied Physics, Part 1: Regular Papers, Short Notes & Review Papers published new progress about 201157-13-3. 201157-13-3 belongs to catalysis-chemistry, auxiliary class Nitro Compound,Amine,Benzene, name is N-Benzyl-2-methyl-4-nitroaniline, and the molecular formula is C14H14N2O2, Name: N-Benzyl-2-methyl-4-nitroaniline.

Hashimoto, Hideki published the artcileSecond-harmonic generation from single crystals of N-substituted 4-nitroanilines, Name: N-Benzyl-2-methyl-4-nitroaniline, the publication is Japanese Journal of Applied Physics, Part 1: Regular Papers, Short Notes & Review Papers (1997), 36(11), 6754-6760, database is CAplus.

Six N-substituted derivatives of 2-methyl-4-nitroaniline (MNA) and two N-substituted derivatives of 4-nitroaniline were synthesized and their phys. and optical properties were examined in the search for nonlinear optical materials with a sufficiently large 2nd harmonic (SH) activity and applicability to practical use. Some derivatives produced single crystals and their structures were determined by x-ray crystallog. The trends of the SH intensity of these materials could be qual. explained based on the b tensor (the effective mol. hyper-polarizability in the crystal). Amongst the derivatives examined N-benzyl-MNA showed the highest SH activity (up to twice that of MNA), thermostability and phase-matching ability.

Japanese Journal of Applied Physics, Part 1: Regular Papers, Short Notes & Review Papers published new progress about 201157-13-3. 201157-13-3 belongs to catalysis-chemistry, auxiliary class Nitro Compound,Amine,Benzene, name is N-Benzyl-2-methyl-4-nitroaniline, and the molecular formula is C14H14N2O2, Name: N-Benzyl-2-methyl-4-nitroaniline.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Hashimoto, H.’s team published research in Journal of Luminescence in 87-89 | CAS: 201157-13-3

Journal of Luminescence published new progress about 201157-13-3. 201157-13-3 belongs to catalysis-chemistry, auxiliary class Nitro Compound,Amine,Benzene, name is N-Benzyl-2-methyl-4-nitroaniline, and the molecular formula is C14H14N2O2, Category: catalysis-chemistry.

Hashimoto, H. published the artcileSecond harmonic generation from the single crystals of N-substituted 4-cyanoanilines, Category: catalysis-chemistry, the publication is Journal of Luminescence (2000), 886-888, database is CAplus.

Six N-substituted derivatives of 4-cyanoaniline (pCA) were synthesized and their phys. and optical properties were examined in the search for 2nd-order nonlinear optical materials with enough crystal dimensions together with blue-light transparency. Among the derivatives examined, N-diphenylmethyl-pCA and N-2-naphthylmethyl-pCA afforded single crystals that lack a center of symmetry. Although the 2nd harmonic (SH) activities of these derivatives were not enough for the practical purposes, their cut-off wavelengths were shorter than 330 nm and showed sufficient blue-light transparency. Quant. prediction of the SH activity was also attempted.

Journal of Luminescence published new progress about 201157-13-3. 201157-13-3 belongs to catalysis-chemistry, auxiliary class Nitro Compound,Amine,Benzene, name is N-Benzyl-2-methyl-4-nitroaniline, and the molecular formula is C14H14N2O2, Category: catalysis-chemistry.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Itoh, Shinichi’s team published research in Tohoku Kogyo Gijutsu Shikensho Hokoku in 16 | CAS: 2016-56-0

Tohoku Kogyo Gijutsu Shikensho Hokoku published new progress about 2016-56-0. 2016-56-0 belongs to catalysis-chemistry, auxiliary class Active Esterification, name is Dodecylamineacetate, and the molecular formula is C14H31NO2, Category: catalysis-chemistry.

Itoh, Shinichi published the artcileFloatability of minerals from the tailings of tin ore dressing, Category: catalysis-chemistry, the publication is Tohoku Kogyo Gijutsu Shikensho Hokoku (1983), 21-6, database is CAplus.

Tantalite??[12178-48-2] is separated from cassiterite??[1317-45-9] by flotation with dodecylamine?acetate??[2016-56-0] because fine grinding is necessary to liberate the minerals and electrostatic separation is difficult to apply. The most important factor in the flotation is the electrochem. property of the solid-liquid interface, and the zeta-potential pH was determined as follows: tantalite 3.5, ilmenite??[12168-52-4], tourmaline, zircon, cassiterite 5.0, monazite??[1306-41-8], xenotime 6.0. Tantalite can be separated from monoazite at low pH because of the difference in zeta-potential, and adsorption of SO42- on the tantalite surface.

Tohoku Kogyo Gijutsu Shikensho Hokoku published new progress about 2016-56-0. 2016-56-0 belongs to catalysis-chemistry, auxiliary class Active Esterification, name is Dodecylamineacetate, and the molecular formula is C14H31NO2, Category: catalysis-chemistry.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Nozaki, Toru’s team published research in Nippon Kagaku Kaishi in | CAS: 2016-56-0

Nippon Kagaku Kaishi published new progress about 2016-56-0. 2016-56-0 belongs to catalysis-chemistry, auxiliary class Active Esterification, name is Dodecylamineacetate, and the molecular formula is C14H31NO2, Application of Dodecylamineacetate.

Nozaki, Toru published the artcileComplex formation of (1-hydroxyethylidene)bisphosphonic acid and flotation with the complexes, Application of Dodecylamineacetate, the publication is Nippon Kagaku Kaishi (1989), 697-701, database is CAplus.

From the polarog. behavior of Cu(II), Pb(II), Cd(II), and Mn(II) ions in (1-hydroxyethylidene)bisphosphonic acid (HEBP, H5L) solutions at an ionic strength of 0.4 mol/dm3 adjusted with sodium perchlorate, the compositions of the metal complexes and their stability constants were determined The species of MH3L, MH2L, MHL2-, M(H3L)22-, M(H3L)H2L3-, M(H2L)24-, and M(H2L)HL5- for Cu and Mn, and same species except MH2L and MHL2- for Cd, were found at pH 4.6-6.4. Species of MHL2-, ML3-, M(OH)L4-, M(HL)26-, and ML28- were found in the pH ranges 11.5-12.9 for Pb(II). The flotation of HEBP by complexing with Fe(III) and the HEBP complexes was investigated. Recoveries of 4.0 ¡Á 10-4 mol/dm3 of HEBP and the HEBP complexes of Cu(II), Pb(II) and Mn(II) were 99.6%, and 99.6, 98.6 and 91.5%, resp., by the flotation for about 5 min using (1.2 ? 1.6) ¡Á 10-3 mol/dm3 of dodecylammonium acetate (DAA) as a surfactant at pH 6.0-9.5. The presence of 6382 ppm of Cl, 3840 ppm of SO42- and 3100 ppm of NO3 did not interfere the flotation. Flotation of HEBP and the complexes proceeds through the formation of ion pair Rn?MHi?L, where n? = 5-n-i?, R and n denoting the cation of DAA and the charge of the metal, resp.

Nippon Kagaku Kaishi published new progress about 2016-56-0. 2016-56-0 belongs to catalysis-chemistry, auxiliary class Active Esterification, name is Dodecylamineacetate, and the molecular formula is C14H31NO2, Application of Dodecylamineacetate.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Matsumura, Fumiko’s team published research in Organic Letters in 10 | CAS: 17351-61-0

Organic Letters published new progress about 17351-61-0. 17351-61-0 belongs to catalysis-chemistry, auxiliary class Phase Transfer Catalyst, name is Tetraethylammonium hydrogencarbonate, and the molecular formula is C9H21NO3, Category: catalysis-chemistry.

Matsumura, Fumiko published the artcileSynthesis of Glycosyl Boranophosphates and Their Applications as Precursors of Glycosyl Phosphate Analogs, Category: catalysis-chemistry, the publication is Organic Letters (2008), 10(8), 1557-1560, database is CAplus and MEDLINE.

Glycosyl boranophosphate triesters were synthesized via a boranophosphorylation of reducing sugars. The usefulness of the resultant glycosyl boranophosphates as versatile chem. stable precursors of various glycosyl phosphate derivatives is demonstrated.

Organic Letters published new progress about 17351-61-0. 17351-61-0 belongs to catalysis-chemistry, auxiliary class Phase Transfer Catalyst, name is Tetraethylammonium hydrogencarbonate, and the molecular formula is C9H21NO3, Category: catalysis-chemistry.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia