Day: April 20, 2022

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 2-(Pyridin-4-yl)-1H-benzo[d]imidazole, is researched, Molecular C12H9N3, CAS is 2208-59-5, about A novel two-dimensional cadmium(II) complex: poly[diaquatris(μ4-cyclohexane-1,4-dicarboxylato)bis[2-(pyridin-4-yl)-1H-benzimidazole]tricadmium(II), the main research direction is crystal structure cadmium pyridinylbenzimidazole cyclohexanedicarboxylato aqua trinuclear complex; mol structure cadmium pyridinylbenzimidazole cyclohexanedicarboxylato aqua trinuclear complex; hydrogen bond cadmium pyridinylbenzimidazole cyclohexanedicarboxylato aqua trinuclear complex; pi stacking cadmium pyridinylbenzimidazole cyclohexanedicarboxylato aqua trinuclear complex; cadmium pyridinylbenzimidazole cyclohexanedicarboxylato aqua trinuclear complex thermal emission property; cadmium complex; crystal structure; dicarboxylate; metal-organic framework; two-dimensional coordination polymer.Computed Properties of C12H9N3.

The title compound, [Cd3(C8H10O4)3(C12H9N3)2(H2O)2]n or [Cd3(chdc)3(4-PyBIm)2(H2O)2]n, was synthesized hydrothermally from the reaction of Cd(CH3COO)2·2H2O with 2-(pyridin-4-yl)-1H-benzimidazole (4-PyBIm) and cyclohexane-1,4-dicarboxylic acid (1,4-chdcH2). The asym. unit consists of one and a half CdII cations, one 4-PyBIm ligand, one and a half 1,4-chdc2- ligands and one coordinated water mol. The central CdII cation, located on an inversion center, is coordinated by six carboxylate O atoms from six 1,4-chdc2- ligands to complete an elongated octahedral coordination geometry. The two terminal rotationally sym. CdII cations each exhibits a distorted pentagonal-bipyramidal geometry, coordinated by one N atom from 4-PyBIm, five O atoms from three 1,4-chdc2- ligands and one O atom from an aqua ligand. The 1,4-chdc2- ligands possess two conformations, i.e. e,e-trans-chdc2- and e,a-cis-chdc2-. The cis-1,4-chdc2- ligands bridge the CdII cations to form a trinuclear {Cd3}-based chain along the b axis, while the trans-1,4-chdc2- ligands further link adjacent one-dimensional chains to construct an interesting two-dimensional network.

After consulting a lot of data, we found that this compound(2208-59-5)Computed Properties of C12H9N3 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

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: 2-Phenylpyridine, is researched, Molecular C11H9N, CAS is 1008-89-5, about Salen-based hypercrosslinked polymer-supported Pd as an efficient and recyclable catalyst for C-H halogenation.Recommanded Product: 2-Phenylpyridine.

The first use of a salen-based hypercrosslinked polymer-supported Pd catalyst to carry out C-H halogenation was reported. This catalyst was effectively catalyze C-H bromination and chlorination even better than its homogeneous counterpart Pd(OAc)2. It also showed excellent reusability without loss of catalytic activity for ten cycles. A broad substrate scope was explored and moderate to excellent yields were obtained.

After consulting a lot of data, we found that this compound(1008-89-5)Recommanded Product: 2-Phenylpyridine can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Product Details of 132098-59-0. 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: Bis((S)-4-phenyl-4,5-dihydrooxazol-2-yl)methane, is researched, Molecular C19H18N2O2, CAS is 132098-59-0, about Concise Enantioselective Synthesis of Oxygenated Steroids via Sequential Copper(II)-Catalyzed Michael Addition/Intramolecular Aldol Cyclization Reactions. Author is Cichowicz, Nathan R.; Kaplan, Will; Khomutnyk, Yaroslav; Bhattarai, Bijay; Sun, Zhankui; Nagorny, Pavel.

A new scalable enantioselective approach to functionalized oxygenated steroids is described. This strategy is based on chiral bis(oxazoline) copper(II) complex-catalyzed enantioselective and diastereoselective Michael reactions of cyclic ketoesters and enones to install vicinal quaternary and tertiary stereocenters. In addition, the utility of copper(II) salts as highly active catalysts for the Michael reactions of traditionally unreactive β,β’-enones and substituted β,β’-ketoesters that results in unprecedented Michael adducts containing vicinal all-carbon quaternary centers is also demonstrated. The Michael adducts subsequently undergo base-promoted diastereoselective aldol cascade reactions resulting in the natural or unnatural steroid skeletons. The exptl. and computational studies suggest that the torsional strain effects arising from the presence of the Δ5-unsaturation are key controlling elements for the formation of the natural cardenolide scaffold. The described method enables expedient generation of polycyclic mols. including modified steroidal scaffolds as well as challenging-to-synthesize Hajos-Parrish and Wieland-Miescher ketones.

After consulting a lot of data, we found that this compound(132098-59-0)Product Details of 132098-59-0 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

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: Nickel(II) chloride ethylene glycol dimethyl ether complex, is researched, Molecular C4H10Cl2NiO2, CAS is 29046-78-4, about Acyl Radicals from α-Keto Acids Using a Carbonyl Photocatalyst: Photoredox-Catalyzed Synthesis of Ketones.Recommanded Product: Nickel(II) chloride ethylene glycol dimethyl ether complex.

Acyl radicals have been generated from α-keto acids RC(O)C(O)OH (R = Ph, furan-2-yl, Me, etc.) using inexpensive and com. available 2-chloro-thioxanthen-9-one as the photoredox catalyst under visible light illumination. These reactive species added to olefins R1CH=CH(R3)R2 [R1 = H, Me, Ph, 4-fluorophenyl, etc.; R2 = H, Me, C(O)OCH3, C(O)OC2H5; R3 = H, C(O)Ph, Boc, (cyclohexyloxy)carbonyl, C(O)OC2H5] or coupled with aryl halides ArX (Ar = Ph, 6-(trifluoromethyl)pyridin-2-yl, quinolin-3-yl, etc.) via a bipyridyl-stabilized Ni(II) catalyst, enabling easy access to a diverse range of ketones ArC(O)R and RC(O)CH(R1)CH(R3)R2. This reliable, atom-economical, and eco-friendly protocol is compatible with a wide range of functional groups.

After consulting a lot of data, we found that this compound(29046-78-4)Recommanded Product: Nickel(II) chloride ethylene glycol dimethyl ether complex can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: Nickel(II) chloride ethylene glycol dimethyl ether complex( cas:29046-78-4 ) is researched.SDS of cas: 29046-78-4.Li, Haoyang; Long, Jiao; Li, Yuqiang; Wang, Wang; Pang, Hailiang; Yin, Guoyin published the article 《Nickel-Catalyzed Regioselective Arylboration of Conjugated Dienes》 about this compound( cas:29046-78-4 ) in European Journal of Organic Chemistry. Keywords: allyl alc arylated preparation arylboration conjugated diene oxidation. Let’s learn more about this compound (cas:29046-78-4).

The nickel-catalyzed arylboration of conjugated dienes CH2:CRCH:CH2 with aryl bromides ArBr and B2pin2, yielding (E)-ArCH2CR:CHCH2OH after oxidation, is reported. Good 1,4-regioselectivity and (E)-stereoselectivity were obtained using isoprene, together with very good 1,2-regioselectivity and (E)-stereoselectivity using 1-arylbutadienes. The high reactivity and selectivity of this process were dependent on the use of the appropriate nitrogen-based ligand. Moreover, wide functional group tolerance was observed under mild reaction conditions. This protocol provides a path to allyl or homoallyl boronic ester derivatives starting from 1,3-dienes, aryl bromides, and B2pin2. The downstream transformation of allyl boronic esters was also achieved, suggesting a strategy for the diastereoselective 1,2-difunctionalization of isoprene and demonstrating the potential for the synthesis of complex mols.

After consulting a lot of data, we found that this compound(29046-78-4)SDS of cas: 29046-78-4 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 2208-59-5, is researched, SMILESS is C1(C2=CC=NC=C2)=NC3=CC=CC=C3N1, Molecular C12H9N3Journal, Article, Research Support, Non-U.S. Gov’t, Journal of Inorganic Biochemistry called Sequence-specific fluorometric recognition of HIV-1 ds-DNA with zwitterionic zinc(II)-carboxylate polymers, Author is Sun, Bin; Zhao, Hai-Qing; Xie, Bao-Ping; Bai, Li-Ping; Jiang, Zhi-Hong; Chen, Jin-Xiang, the main research direction is HIV1 DNA fluorescent probe zwitterionic zinc carboxylate polymer; organic metal framework zwitterionic zinc carboxylate polymer synthesis; Crystal structure; Fluorescence detection; HIV-1 ds-DNA recognition; Water-stable MOF.Application In Synthesis of 2-(Pyridin-4-yl)-1H-benzo[d]imidazole.

Four water-stable zwitterionic zinc-carboxylate polymers are prepared by reacting N-carboxymethyl-(3,5-dicarboxy)-pyridinium bromide (H3CmdcpBr) with zinc(II) nitrate in the presence of NaOH, through adjusting the solvents and ancillary ligands. With H2O as the solvent and the absence of an ancillary ligand, a two-dimensional (2D) polymer network [Zn(Cmdcp)(H2O)]n (1) is formed. In a mixed H2O/DMF solvent and with the presence of chelating ligands 2,2′-bipyridine (bipy), 1,10-phenanthroline (phen) and 2-(4-pyridyl)benzimidazole (pbz), a one-dimensional (1D) polymer of {[Zn2(Cmdcp)(bipy)2(H2O)5](NO3)2·3H2O}n (2), a mononuclear ionic species of [Zn(phen)(H2O)4][Cmdcp] (3), and a 2D polymer of {[Zn(Cmdcp)(pbz)][pbz]·7H2O}n (4) are accordingly formed. Compounds 1-4 are characterized by IR, elemental analyses and single crystal X-ray crystallog. Compound 2 strongly adsorbs single-stranded DNA (ss-DNA) probe (denoted as P-DNA) labeled with carboxyfluorescein (FAM) and quenches its fluorescence via a photo-induced electron transfer process. If, however, a double-stranded DNA (ds-DNA) of the human immunodeficiency virus 1 (HIV-1 ds-DNA) is further present, the P-DNA interacts with the major groove in HIV-1 ds-DNA via Hoogsteen hydrogen bonding to form a rigid triplex structure. This results in partial or complete fluorescence recovery depending on the concentration of HIV-1 ds-DNA. The findings are applied in fluorometric sensing of HIV-1 ds-DNA. The calibration plot is linear in the 0-60 nM target DNA concentration range, with a 7.4 nM detection limit (at a signal-to-noise ratio of 3). The assay is highly specific and not interfered by one base pair mutated for complementary target HIV-1 ds-DNA, complementary ss-DNA, single-base pair mutated for complementary ss-DNA, non-specific ss-DNA sequences, and higher-order dimeric G-quadruplexes.

After consulting a lot of data, we found that this compound(2208-59-5)Application In Synthesis of 2-(Pyridin-4-yl)-1H-benzo[d]imidazole can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Product Details of 76-60-8. 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: 3,3-Bis(3,5-dibromo-4-hydroxy-2-methylphenyl)-3H-benzo[c][1,2]oxathiole 1,1-dioxide, is researched, Molecular C21H14Br4O5S, CAS is 76-60-8, about One-step fabrication of Fe2O3/Mn2O3 nanocomposite for rapid photodegradation of organic dyes at neutral pH. Author is Ghaffari, Yasaman; Gupta, Nishesh Kumar; Bae, Jiyeol; Kim, Kwang Soo.

In this study, a novel coral-like Fe2O3/Mn2O3 nanocomposite (FMNC) was synthesized by a one-step surfactant-mediated co-precipitation method. The application of this material was demonstrated for the degradation of organic dyes. The crystallog. anal. of FMNC confirmed the presence of α-Fe2O3 and α-Mn2O3 with no impurity of MnFe2O4. The photocatalyst showed strong absorbance in the UV and Visible range with a low bandgap energy of 1.11 eV. In the optimized exptl. conditions (0.5 g L-1 photocatalyst, 10 mg L-1 MB concentration, and 5 mmol L-1 H2O2), the FMNC photocatalyst showed 80-97% degradation of organic dyes within 75 s using low power UV-C irradiation Moreover, scavenger studies confirmed the involvement of ·OH radicals and holes as the main active species responsible for the dye degradation process. The photocatalytic degradation process was insignificantly affected by the presence of inorganic anions. The photocatalyst showed a ∼ 5% loss of performance after seven photocatalytic cycles. This study concluded that UV/H2O2/FMNC system is a fast, efficient, and economical approach for remediation of dye-contaminated wastewater.

After consulting a lot of data, we found that this compound(76-60-8)Product Details of 76-60-8 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Generation and oxidative reactivity of a Ni(II) superoxo complex via ligand-based redox non-innocence, published in 2020, which mentions a compound: 29046-78-4, Name is Nickel(II) chloride ethylene glycol dimethyl ether complex, Molecular C4H10Cl2NiO2, Related Products of 29046-78-4.

Metal ligand cooperativity is a powerful strategy in transition metal chem. This type of mechanism for the activation of O2 is best exemplified by heme centers in biol. systems. While aerobic oxidations with Fe and Cu are well precedented, Ni-based oxidations are frequently less common due to less-accessible metal-based redox couples. Some Ni enzymes utilize special ligand environments for tuning the Ni(II)/(III) redox couple such as strongly donating thiolates in Ni superoxide dismutase. A recently characterized example of a Ni-containing protein, however, suggests an alternative strategy for mediating redox chem. with Ni by utilizing ligand-based reducing equivalent to enable oxygen binding. While this mechanism has little synthetic precedent, authors show here that Ni complexes of the redox-active ligand tBu,TolDHP (tBu,TolDHP = 2,5-bis((2-t-butylhydrazono)(p-tolyl)methyl)-pyrrole) activate O2 to generate a Ni(II) superoxo complex via ligand-based electron transfer. This superoxo complex is competent for stoichiometric oxidation chem. with alcs. and hydrocarbons. This work demonstrates that coupling ligand-based redox chem. with functionally redox-inactive Ni centers enables oxidative transformations more commonly mediated by metals such as Fe and Cu.

After consulting a lot of data, we found that this compound(29046-78-4)Related Products of 29046-78-4 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

SDS of cas: 76-60-8. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 3,3-Bis(3,5-dibromo-4-hydroxy-2-methylphenyl)-3H-benzo[c][1,2]oxathiole 1,1-dioxide, is researched, Molecular C21H14Br4O5S, CAS is 76-60-8, about Experimental investigation on CO2 absorption and physicochemical characteristics of different carbon-loaded aqueous solvents. Author is Perumal, Muthumari; Karunakaran, Nilavuckkarasi R.; Balraj, Ambedkar; Jayaraman, Dhanalakshmi; Krishnan, Jagannathan; Prakash, Aalan Britto John; Arumugam, Jeevakumar; Muthukumar, Venkadeshwara Prabhu.

Abstract: The anthropogenic carbon dioxide (CO2) denseness in the earth’s atm. is increasing day-to-day by combusting fossil fuels for power generation. And, it is the most important greenhouse gas (GHG) responsible for 64% of global warming. Solvent-based carbon capture gained more attention towards researchers because of its easiness to integrate with the coal-fired power plant without significant modifications. During CO2 absorption, the phys. property of the solvent gets changed. A change in the solvent’s physicochem. property affects further CO2 absorption, thereby increasing the carbon-capture energy demand. The present exptl. study encompasses CO2 absorption studies using 30 wt% aqueous monoethanolamine (MEA), 2-amino-2-methyl-1-propanol (AMP) and piperazine (PZ) followed by the detailed anal. of physicochem. properties (pH, carbon loading (α), viscosity (μ), d. (ρ) and surface tension (σ)) of various CO2-loaded solutions The results revealed that these properties are exhibiting interdependent eccentrics. Furthermore, an empirical model was developed to predict the carbon loading of the tested solvents. This model includes the tested physicochem. properties, reaction mixture temperature, diffusivity and change in the mass of solvent during carbon loading. In addition, an empirical model for viscosity as a function of temperature, carbon loading and mol. weight of solvents was developed.

After consulting a lot of data, we found that this compound(76-60-8)SDS of cas: 76-60-8 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Product Details of 2208-59-5. 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-(Pyridin-4-yl)-1H-benzo[d]imidazole, is researched, Molecular C12H9N3, CAS is 2208-59-5, about Four new compounds based on terephthalate and 2-(4-pyridyl)benzimidazole ligands. Author is Xia, Chang-Kun; Wu, Yun-Long; Xie, Ji-Min.

Four compounds based on H2BDC and PyBIm [H2BDC = 1,4-benzenedicarboxylic acid, PyBIm = 2-(4-pyridyl)benzimidazole], (PyBIm)(H2BDC)0.5 (1), Co(PyBIm)2(HBDC)(BDC)0.5 (2), Ni(PyBIm)2(HBDC)(BDC)0.5 (3), and Zn(BDC)(PyBIm).H2O (4), were synthesized by hydrothermal methods and characterized by x-ray diffraction. Compound 1 contains 2 types of H-bonding N-H···N and O-H···N, which connect the mols. into a 2D layer. Complex 2 crystallizes isostructural to 3 in triclinic space group P1̅, in 1D chains. The H-bonding interactions between uncoordinated N, N-H, and COOH groups in 2 connect the 1D chains into a 2D layer. Complex 4 displays a 1D structure, which is finally extended to a 3D supramol. framework by H-bonding and π-π packing interactions. The magnetic properties of 2 and 3 were studied as well.

After consulting a lot of data, we found that this compound(2208-59-5)Product Details of 2208-59-5 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles