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Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: Aluminum(III) sulfate xhydrate, is researched, Molecular Al2H8O13S3, CAS is 17927-65-0, about Tribochemistry and kinetics of Al2(SO4)3.xH2O decomposition.Related Products of 17927-65-0.

The thermal decomposition of tribochem. activated Al2(SO4)3.xH2O was studied by TG, DTA and EMF methods. For some of the intermediate solids, x-ray diffraction and IR-spectroscopy were applied to learn more about the reaction mechanism. Thermal and EMF studies confirmed that, even after mech. activation of Al2(SO4)3.xH2O, Al2O(SO4)2 is formed as an intermediate. Isothermal kinetic experiments demonstrated that the thermochem. sulfurization of inactivated Al2(SO4)3.xH2O has an activation energy of 102.2 kJ.mol-1 in the temperature range 850-890 K. The activation energy for activated Al2(SO4)3.xH2O in the range 850-900 K is 55.0 kJ.mol-1. The time of thermal decomposition is almost halved when Al2(SO4)3.xH2O is activated mech. The results permit conclusions concerning the efficiency of the tribochem. activation of Al2(SO4)3.xH2O and the chem. and kinetic mechanisms of the desulfurization process.

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A new synthetic route of 560-09-8

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SDS of cas: 560-09-8. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: (1S,3R)-1,2,2-Trimethylcyclopentane-1,3-dicarboxylic acid, is researched, Molecular C10H16O4, CAS is 560-09-8, about Stereo- and enantio-selective hydrogenation of ketones using iridium catalysts containing a carboxylate ligand. Author is Heil, Balint; Kvintovics, Pal; Tarszabo, Laszlo; James, Brian R..

Cyclohexanone I and PhCOMe were hydrogenated in Me2CHOH under Ar in the presence of a catalyst formed from [IrCl(C8H14)2]2, a carboxylic acid, and P(OR2)3 (R2 = Bu, Ph, Me). For I the best carboxylic acids were BzOH, AcOH, (R)-(-)-PhCH(OH)CO2H (II) (R)-(+)-HO2CCH2CH(OH)CO2H, MeCH:CHCO2H and PhCH:CHCO2H. (RS)-PhCH(OAc)CO2H, EtCO2H and (1S,3R)-camphoric acid gave lower conversions. Conversion was increased to 78% when Et3N was added and the catalyst contained BzOH and P(OMe)3. The cis/trans ratio was 1.8. The cis/trans ratio increased as the P(OMe)3-Ir ratio increased to ∼4, and then decreased. PhCOMe conversion to (S)-PhCH(OH)Me was 75% and an optical yield of 1.0% was obtained by P(OMe)3, II, and NaOMe. Using (S)-(+)-PhCH(OH)CO2H an excess of (R)-PhCH(OH)Me was obtained. (R)-(-)-PhCH(OAc)CO2H gave 12% enantiomeric excess of S-isomer with 20% conversion.

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In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called A facile construction of 4-hydroxymethylbenzisothiazolone-1,1-dioxide, published in 1998-03-19, which mentions a compound: 119639-24-6, mainly applied to furylmethanol isothiazolone dioxide regioselective Diels Alder; hydroxymethylbenzisothiazolone regioselective preparation; benzisothiazolone hydroxymethyl regioselective preparation; MO Diels Alder furylmethanol isothiazolone dioxide; hydrogen bond furylmethanol isothiazolone dioxide cycloaddition, Related Products of 119639-24-6.

4-Hydroxymethylbenzisothiazolone-1,1-dioxide could be facilely synthesized via a highly regioselective Diels-Alder cycloaddition between furfuryl alc. and 2-(tert-butyl)-isothiazolone-1,1-dioxide, followed by aromatization of the adduct under basic conditions. A secondary effect from intramol. hydrogen bonding influences the regioselectivity of the cycloaddition Unequivocal proof of the regiochem. of the Diels-Alder reaction is provided by X-ray crystallog. and ab initio calculations showed electronic and steric effects on transition structure asynchronicity.

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Little discovery in the laboratory: a new route for 560-09-8

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Name: (1S,3R)-1,2,2-Trimethylcyclopentane-1,3-dicarboxylic acid. 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. Compound: (1S,3R)-1,2,2-Trimethylcyclopentane-1,3-dicarboxylic acid, is researched, Molecular C10H16O4, CAS is 560-09-8, about Resolution of the racemates of DL-carnitine.

A rational and cheap method is reported for the direct resolution of DL-carnitine. D-(+)-Camphoric acid, L-(-)-camphoric acid, dibenzoyl-D-(-)-tartaric acid, or L-(+)-tartaric acid were used to sep. DL-carnitine into its optically active components. Resolution was achieved by repeated fractional crystallization in alc. solution with the appropriate acid, or by combined fractionation with a suitable pair of acids. The resulting salts can be decomposed quant. with water, dilute acids, ether/water, or ion exchanger, to give pure, optically active carnitines. The optically active acids may also be recovered pure and used again for racemate separation

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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: 2-Amino-6-methylpyrimidine-4-thiol( cas:6307-44-4 ) is researched.Quality Control of 2-Amino-6-methylpyrimidine-4-thiol.Felczak, Krzysztof; Bretner, Maria; Kulikowski, Tadeusz; Shugar, David published the article 《High-yield regioselective thiation of biologically important pyrimidinones, dihydropyrimidinones and their ribo, 2′-deoxyribo and 2′,3′-dideoxyribo nucleosides》 about this compound( cas:6307-44-4 ) in Nucleosides & Nucleotides. Keywords: pyrimidinone regioselective thiation Lawesson reagent; nucleoside pyrimidinone regioselective thiation Lawesson reagent. Let’s learn more about this compound (cas:6307-44-4).

Convenient and high-yield regioselective thiation procedures based on the use of the Lawesson reagent in different solvents, are described for conversion of the 2- and 4-keto, and 2,4-diketo pyrimidines to the corresponding 2(4)-thio, and 2,4-dithio, derivatives This method is applicable to thiation of the 4-keto groups of 5,6-dihydropyrimidinones and pyrimidine nucleosides. The mild reaction conditions employed are such that it is the method of choice for compounds with labile glycosidic bonds, of choice for compounds with labile glycosidic bonds, such as 5,6-dihydropyrimidine nucleosides and the 2′,3′-dideoxynucleosides currently of interest as antiretroviral, including anti-HIV, agents.

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COA of Formula: Al2H8O13S3. 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: Aluminum(III) sulfate xhydrate, is researched, Molecular Al2H8O13S3, CAS is 17927-65-0, about The effect of the composition and of the calcination regimes of a mixture of aluminum and magnesium sulfates on the formation process of spinels. Author is Sokol, V. A.; Rokhlenko, D. A.; Kononova, L. I..

During calcination of MgSO4-Al2(SO4)3.18H2O mixtures the completion of the formation of Al2MgO4 depends on excess H2SO4 or (NH4)2SO4 and on the rate of heating ≤1300°. The optimum parameters for the formation of Al2MgO4 are: H2SO4 content in Al2(SO4)3.18H2O is 0.5-3 mass%, region of thermal treatment is continuous, rate of increase of temperature is 300-600° h-1 and isothermal heating for 3-6 h at 1300°.

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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: Aluminum(III) sulfate xhydrate( cas:17927-65-0 ) is researched.Product Details of 17927-65-0.Hilal, Nidal; Busca, Gerald; Talens-Alesson, Federico; Atkin, Brian P. published the article 《Treatment of waste coolants by coagulation and membrane filtration》 about this compound( cas:17927-65-0 ) in Chemical Engineering and Processing. Keywords: waste coolant coagulation membrane filtration. Let’s learn more about this compound (cas:17927-65-0).

The treatment of waste coolant (Mobilcut 232) from cutting tools was studied by 3 processes. The 1st pre-treatment process, coagulation was tested using 4 conventional industrial coagulants, Al sulfate hydrate, Al chloride, Fe sulfate pentahydrate and Fe chloride. The 2nd process was filtering the supernatant produced from the 1st stage using 2 nanofiltration membranes of 500 and 2000 Da. The 3rd process used ultrafiltration method using a 100,000 Da membrane. The critical coagulation concentration of the different coagulants was determined and the quality of the supernatant was compared to the permeate produced by ultrafiltration. The parameters compared were TOC, absorbance at 400 nm and pH. The performances of both nanofiltration membranes were evaluated. The surface morphol. and pore size distribution of the NF and UF membranes were studied with an at. force microscope.

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Reference of Aluminum(III) sulfate xhydrate. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Aluminum(III) sulfate xhydrate, is researched, Molecular Al2H8O13S3, CAS is 17927-65-0, about Increase in the hydration activity and improvement in the structural-engineering properties of slag portland cement. Author is Syrkin, Ya. M.; Shokotova, B. G.; Engorn, T. I.; Tokar, V. A.; Zubik, M. I..

The sulfate-aluminate-silicate product, obtained as a tailing in the production of Al sulfate from kaolin clays, is used as an hardening accelerator for slag portland cement. The tailings consist of amorphous SiO2, metakaolinite [15123-81-6], Al2(SO4)3.nH2O, NaAl(SO4)2.12H2O, gypsum [13397-24-5], anhydrite [14798-04-0], and some Fe and Mg sulfates. Initial and final setting times and compressive and tensile strengths are determined of slag portland cements with 1 and 3% of these tailings and those with 1% coke dust. These additives increase the hydration activity of the slag portland cement and its frost resistance and decrease the shrinkage deformation.

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Formula: C7H11NO3S. 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: 2-(tert-Butyl)isothiazol-3(2H)-one 1,1-dioxide, is researched, Molecular C7H11NO3S, CAS is 119639-24-6, about Synthesis of new biologically active isothiazolo[4,5-b]carbazole-type tetracyclic derivatives via an indole-2,3-quinodimethane approach. Author is Miambo, Raimundo F.; Laronze-Cochard, Marie; Lawson, Ata-Martin; Guillot, Regis; Baldeyrou, Brigitte; Lansiaux, Amelie; Supuran, Claudiu T.; Sapi, Janos.

A number of isothiazolo[4,5-b]carbazole derivatives were prepared via a Diels-Alder approach involving thermally induced indole-2,3-quinodimethane intermediates. Preliminary biol. tests revealed a GSK-3β kinase inhibitor (I) and some free NH group containing compounds (I, II, III) displayed selective human carbonic anhydrase I inhibitory activities.

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Quality Control of (1S,3R)-1,2,2-Trimethylcyclopentane-1,3-dicarboxylic acid. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: (1S,3R)-1,2,2-Trimethylcyclopentane-1,3-dicarboxylic acid, is researched, Molecular C10H16O4, CAS is 560-09-8, about Two Homochiral Bimetallic Metal-Organic Frameworks Composed of a Paramagnetic Metalloligand and Chiral Camphorates: Multifunctional Properties of Sorption, Magnetism, and Enantioselective Separation. Author is Ryu, Dae Won; Lee, Woo Ram; Lim, Kwang Soo; Phang, Won Ju; Hong, Chang Seop.

Two porous metal-organic frameworks [Co(Tt)2][Cu4(D-cam)4]·5H2O·DMF (1; Tt = tris(triazolyl)borate, D-H2cam = D-(+)-camphoric acid or (1R,3S)-1,2,2-trimethyl-1,3-cyclopentanedicarboxylic acid) and [Co(Tt)2][Cu4(L-cam)4]·5H2O·2DMF (2; L-H2cam = L-(-)-camphoric acid or (1S,3R)-1,2,2-trimethyl-1,3-cyclopentanedicarboxylic acid) were prepared by mixing Cu2+, Co(Tt), and camphoric acid under solvothermal conditions. The structures of 1 and 2 reveal that the two-dimensional layers composed of chiral ligands and Cu-Cu paddlewheel units are connected through the metalloligands to form three-dimensional networks. These solids show multifunctional properties such as gas adsorption onto the pores of the frameworks, antiferromagnetic coupling between spin carriers, and a small enantioselective separation of racemic alcs.

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