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The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: 1-(Bromomethyl)-4-ethylbenzene(SMILESS: CCC1=CC=C(CBr)C=C1,cas:57825-30-6) is researched.Application In Synthesis of 5,5′-Dimethyl-2,2′-bipyridine. The article 《Substituent effects on benzylic radical hydrogen hyperfine coupling constants. Part 4. The effect of branching of the alkyl substituent》 in relation to this compound, is published in Canadian Journal of Chemistry. Let’s take a look at the latest research on this compound (cas:57825-30-6).

The substituent effects on the title hfc constants of m- (I) or p-R1C6H4R2• (II; R = H, Me) are discussed and the ESR of II (R = H, Me; R1 = Me, Et, Me2CH, Me3C) are analyzed. ESR and INDO calculations show that hyperconjugation involving the C-C bond is 40-60% as effective as C-H hyperconjugation for delocalizing spin d. 13C NMR of p-R1C6H4C+Me2 shows that C-C hyperconjugation is 75-90% as effective as C-H hyperconjugation for delocalizing charge d. The inductive effect on the hfc were deted. by the LFER with σm for I; the inductive withdrawal of electron d. leads to a decrease in spin delocalization.

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Application of 19777-66-3. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: (S)-Propane-1,2-diamine dihydrochloride, is researched, Molecular C3H12Cl2N2, CAS is 19777-66-3, about Resolution of propandiamine and synthesis of dexrazoxane. Author is Wang, Yuling; Song, Hongrui; Song, Aihua.

The resolution of propandiamine and synthesis of dexrazoxane were studied. Using 1,2-propandiamine as primary material, the synthetic method of dexrazoxane by resolution, alkylation and cyclization was established. The L-tartaric acid was used as a resolving reagent, 1,2-propandiamine was resolved and the (+)-enantiomer was obtained. The method of changing 1,2-propandiamine bitartrate into hydrochloride was improved. The method was simpler and might be of application.

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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.Shrader, William D.; Celebuski, Joseph; Kline, Steven J.; Johnson, David researched the compound: 8-Hydroxyquinoline 1-oxide( cas:1127-45-3 ).COA of Formula: C9H7NO2.They published the article 《Synthesis of a novel hexadentate chelating agent based on 8-hydroxyquinoline》 about this compound( cas:1127-45-3 ) in Tetrahedron Letters. Keywords: hydroxyquinolinecarbonamidoethylamine preparation hexadentate chelating agent; quinolinecarbonamidoethylamine preparation chelating agent; amidation succinimido hydroxyquinolinecarboxylate aminoethylamine. We’ll tell you more about this compound (cas:1127-45-3).

Tris[[(hydroxyquinoline)carbonamido]ethyl]amine (I), a new hexadentate chelator, was prepared by the conversion of 8-hydroxyquinoline to succinimido hydroxyquinolinecarboxylate II and subsequent reaction with N(CH2CH2NH2)3. I is a siderophore analog with a non-naturally occurring binding unit comprising a combination of both O and N donor atoms.

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Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Tetrahedron called Construction of polyaromatics via photocyclization of 2-(fur-3-yl)ethenylarenes, using a 3-furyl group as an isopropenyl equivalent synthon, Author is Chen, Ying-Zhe; Ni, Ching-Wen; Teng, Fu-Lin; Ding, Yi-Shun; Lee, Tunng-Hsien; Ho, Jinn-Hsuan, which mentions a compound: 57825-30-6, SMILESS is CCC1=CC=C(CBr)C=C1, Molecular C9H11Br, Safety of 1-(Bromomethyl)-4-ethylbenzene.

The construction of different types of substituted arenes was demonstrated through the photocyclization of 2-(fur-3-yl)ethenylarenes using a 3-furyl group as an isopropenyl equivalent synthon in the photocyclization reaction. The furan portion of the photocyclization intermediate could be fragmented via a base-induced elimination reaction to yield a series of substituted polyaromatics, including naphthalene, benzofuran, benzothiophene, phenanthrene, phenalene, acenaphthene, and triphenylene. Using different reagents, this method made it possible to introduce Me or 2-hydroxyethyl groups as substituents at specific positions in these arenes.

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The reaction of an aromatic heterocycle with a proton is called a protonation. One of articles about this theory is 《Low-dimensional compounds containing bioactive ligands. Part XVI: Halogenated derivatives of 8-quinolinol N-oxides and their copper(II) complexes》. Authors are Lukoova, Andrea; Baran, Peter; Volarevic, Vladislav; Ilic, Aleksandar; Vilkova, Maria; Litecka, Miroslava; Harmosova, Michaela; Potocnak, Ivan.The article about the compound:8-Hydroxyquinoline 1-oxidecas:1127-45-3,SMILESS:OC1=CC=CC2=CC=C[N+]([O-])=C12).Recommanded Product: 8-Hydroxyquinoline 1-oxide. Through the article, more information about this compound (cas:1127-45-3) is conveyed.

Four N-oxides, 8-quinolinol N-oxide (8-HQNO), 5,7-dichloro-8-quinolinol N-oxide (HdClQNO), 5,7-dibromo-8-quinolinol N-oxide (HdBrQNO) and 7-iodo-8-quinolinol N-oxide (HIQNO) as well as their six copper complexes, CuCl2(8-HQNO)2(H2O) (1), CuCl2(HdClQNO)2(H2O)2 (2), Cu(dClQNO)2(CHCl3) (3), Cu(dClQNO)2(H2O) (4), {[Cu(dBrQNO)2]•2H2O}n (5) and CuCl2(HIQNO)2(H2O)4 (6) were synthesized as possible anticancer agents. Crystal structures of N-oxides contain planar mols. held together via hydrogen bonds involving oxygen atoms of N-oxide groups as acceptors. Crystal structure of 5 represents the first structure of a copper(II) complex with an N-oxide ligand derived from 8-HQNO and is formed by infinite chains. In the chain, the Cu(II) atom coordinates to six oxygen atoms from two bidentate chelating dBrQNO ligands occupying apexes of elongated tetragonal bipyramid with bridging oxygen atoms of N-oxide groups in axial positions. Antiproliferative activity of prepared N-oxides as well as their complexes was studied using in vitro MTT assay against the MDA-MB-231, HCT-116 and A549 cancer cell lines and their selectivity was verified on MSCs cells. Among the tested cancer cell lines, A549 and MDA-MB-231 cells were the most sensitive to the tested complexes. Complex 1 showed the highest cytotoxicity against both tumor cell lines. At concentration, which could be tested in animal models, 1 induced cell death in >50% of cancer cells and in 20% of MSCs indicating its selectivity.

In some applications, this compound(1127-45-3)Recommanded Product: 8-Hydroxyquinoline 1-oxide is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

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Application In Synthesis of 8-Hydroxyquinoline 1-oxide. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 8-Hydroxyquinoline 1-oxide, is researched, Molecular C9H7NO2, CAS is 1127-45-3, about Intramolecular hydrogen bonding in 8-quinolinol N-oxides, quinaldinic acid N-oxides and quinoline-2-carboxyamide N-oxide. Deuterium isotope effects on 13C chemical shifts. Author is Dziembowska, Teresa; Rozwadowski, Zbigniew; Hansen, Poul Erik.

Secondary isotope effects on 13C chem. shifts have been measured in a series quinolinols, quinaldinic acid N-oxides and quinoline-2-carboxyamide N-oxide. For 8-quinolinol N-oxides a good correlation was found between δOH and nΔC(OD) isotope effects. The OH and 13C chem. shifts and nΔC(OD) show very small temperature dependences. The primary isotope effects are small, pos. and temperature insensitive. Furthermore, they increase with increasing nΔC(OD). All features point towards a localized hydrogen bond in an asym. double well potential. The quinaldinic acid N-oxides show long-range isotope effects on 13C chem. shifts of both signs with 2ΔC=O(OD) rather small. The primary isotope effects of the quinaldinic acid N-oxide is of order of 0.5 ppm, whereas for its 4-ethoxy-derivative is smaller, ∼0.3 ppm. The OH chem. shifts resonate at the low field ∼18-20 ppm and the OH resonance is fairly broad at room temperature, especially for the 4-ethoxy-derivative The temperature effects on the chem. shifts, primary and secondary isotope effects are small. For quinaldinic acid N-oxides the asym. broad quasi-single potential is suggested.For quinoline-2-carboxyamide N-oxide the isotope effects are small, indicating rather weak hydrogen bond.

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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.Chang, Qing; Luo, Zeshunji; Fu, Licai; Zhu, Jiajun; Yang, Wulin; Li, Deyi; Zhou, Lingping researched the compound: Nickel(ii)fluoridetetrahydrate( cas:13940-83-5 ).Safety of Nickel(ii)fluoridetetrahydrate.They published the article 《A new cathode material of NiF2 for thermal batteries with high specific power》 about this compound( cas:13940-83-5 ) in Electrochimica Acta. Keywords: cathode nickel fluoride thermal battery. We’ll tell you more about this compound (cas:13940-83-5).

Transition metal halides, especially fluorides, are promising candidates used as cathode materials for primary batteries, thanks to their attractive electrochem. properties such as high conversion potential as well as extraordinary specific capacity. The intrinsic thermal stability stemming from the characteristic ionic bond, M-F, also enables them to be applied in some severe conditions. Herein, the authors study the discharge performance of NiF2 under large c.d. (0.1 A cm-2, 0.2 A cm-2 and 0.5 A cm-2), together with extremely high temperature of 520°, 550° and 580°. It can exhibit excellent electrochem. properties with the maximum specific power up to 16.2 kW kg-1 at c.d. of 0.5 A cm-2 and temperature of 550°, at cutoff voltage of 2 V (80% of the peak voltage). When the c.d. is controlled at 0.1 A cm-2, the specific power can also reach at 3.5 kW kg-1 with other parameters as the same. Afterwards, XRD and XPS are conducted to further evidence the discharge mechanism of this process, confirming it as NiF2 + 2Li → Ni + 2LiF. Based on them, probably this work will afford insights into alternatives of cathode materials in the area of high specific power thermal batteries.

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Category: quinoxaline. 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: 1-(Bromomethyl)-4-ethylbenzene, is researched, Molecular C9H11Br, CAS is 57825-30-6, about Synthesis of novel blue light emitting 9,9′-bianthracene derivatives and their optoelectronic properties.

A series of novel blue light emitting materials 9,9′-bianthracene derivatives have been designed and synthesized by introducing different substituent groups through Suzuki coupling reactions. Their structure was identified by H NMR and UV-Vis absorption and fluorescence emission; Moreover, their fluorescence quantum efficiency and electrochem. properties were characterized in detail. The results indicate that all these compounds emit blue light, compared with 9,9′-bianthracene, the maximum emission peak of these materials is at 453 nm, red shift of 7 nm, and it is the typical blue fluorescence. This is because these derivatives have a non planar geometric structure. These derivatives also present high fluorescence quantum efficiency and are 1.18-1.43 times as much as that of 9,9′-bianthracene. In addition, their redox actives are also improved. Consequently, it was believed that these derivatives are potential ideal blue light fluorescent materials.

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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: (S)-Propane-1,2-diamine dihydrochloride, is researched, Molecular C3H12Cl2N2, CAS is 19777-66-3, about Cold Crystallization of Chiral Schiff-Base Nickel(II) Complex Having Alkyl Chains and a Characteristic Methyl Group.Related Products of 19777-66-3.

Mols. exhibiting cold crystallization, an exothermic phenomenon in heating following supercooling, can be used as a heat storing material. However, examples in nonpolymers are still few. A chiral Schiff-base nickel(II) complex, which had a characteristic Me group and long alkyl chains, exhibited complicated thermal behavior including cold crystallization The Me group was a steric barrier to dimerization and mol. stacking, leading to the supercooled state. The thermal behavior of enantiomer was different from that of racemate.

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The reaction of an aromatic heterocycle with a proton is called a protonation. One of articles about this theory is 《Heterocyclic N-oxides. III. 8-Hydroxyquinoline N-oxide》. Authors are Ramaiah, K.; Srinivasan, V. R..The article about the compound:8-Hydroxyquinoline 1-oxidecas:1127-45-3,SMILESS:OC1=CC=CC2=CC=C[N+]([O-])=C12).Synthetic Route of C9H7NO2. Through the article, more information about this compound (cas:1127-45-3) is conveyed.

cf. CA 57, 6761f. Unlike 8-hydroxyquinoline (I), the title compound (II) shows no OH stretching at 3400 or 3660 cm.-1, Badger and Moritz (CA 53, 11382g). The broad medium-intensity band of II at 2857-2440 cm.-1 is independent of concentration and is interpreted as evidence of strong intramol. H bonding involving the O-H and N-O groups. Preliminary study by the method of Irving, et al. (CA 43, 8941i) with 23 cations indicates that II chelates more selectively than I. The results at pH 5.2, 8.4, and 12.4 are tabulated. II is conveniently prepared in fair yield by heating (water bath, 65-75°) 14.5 g. I in 30 ml. glacial HOAc with 10 ml. 30% H2O2. At intervals of 1 hr. a total of 30 ml. more of H2O2 was added in 3 equal increments. The mixture was concentrated in vacuo, made alk. with saturated aqueous Na2CO3, and left overnight after addition of 60 ml. CHCl3. Unreacted I was removed by steam distillation of the mixture after filtration, drying and removal of CHCl3 by distillation Hot filtration of the aqueous residue gave on cooling 5.96 g. yellow needles of II, m. 139°.

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