Category: 110-52-1

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 1,4-Dibromobutane( cas:110-52-1 ) is researched.Category: indole-building-block.Deng, Ke-Zuan; Jia, Wen-Liang; Angeles Fernandez-Ibanez, M. published the article 《Selective Para-C-H Alkynylation of Aniline Derivatives by Pd/S,O-Ligand Catalysis》 about this compound( cas:110-52-1 ) in Chemistry – A European Journal. Keywords: alkynyl dibenzylaniline preparation; silyl alkynyl iodide dibenzylaniline alkynylation regioselective; C−H activation; S,O-ligand; alkynylation; aniline; palladium. Let’s learn more about this compound (cas:110-52-1).

Herein, authors report a nondirected para-selective C-H alkynylation of aniline derivatives by a Pd/S,O-ligand-based catalyst. The reaction proceeds under mild conditions and is compatible with a variety of substituted anilines. The scalability and further derivatizations of the alkynylated products have been also demonstrated.

Different reactions of this compound(1,4-Dibromobutane)Category: indole-building-block require different conditions, so the reaction conditions are very important.

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: 1,4-Dibromobutane( cas:110-52-1 ) is researched.Category: indole-building-block.Deng, Ke-Zuan; Jia, Wen-Liang; Angeles Fernandez-Ibanez, M. published the article 《Selective Para-C-H Alkynylation of Aniline Derivatives by Pd/S,O-Ligand Catalysis》 about this compound( cas:110-52-1 ) in Chemistry – A European Journal. Keywords: alkynyl dibenzylaniline preparation; silyl alkynyl iodide dibenzylaniline alkynylation regioselective; C−H activation; S,O-ligand; alkynylation; aniline; palladium. Let’s learn more about this compound (cas:110-52-1).

Herein, authors report a nondirected para-selective C-H alkynylation of aniline derivatives by a Pd/S,O-ligand-based catalyst. The reaction proceeds under mild conditions and is compatible with a variety of substituted anilines. The scalability and further derivatizations of the alkynylated products have been also demonstrated.

Different reactions of this compound(1,4-Dibromobutane)Category: indole-building-block require different conditions, so the reaction conditions are very important.

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

Abbasi Boji, Massomeh; Ghorbanloo, Massomeh published the article 《Synthesis, characterization, and fabrication of silver nanoparticles in 1-vinyl imidazole-based hydrogels and their use in olefin oxidation, hydrogen generation, and oxo-anion adsorption》. Keywords: olefin vinyl imidazole silver nanoparticle hydrogel oxidation adsorption.They researched the compound: 1,4-Dibromobutane( cas:110-52-1 ).HPLC of Formula: 110-52-1. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:110-52-1) here.

Poly(1-vinylimidazole), (p(1-VIm)), hydrogels were synthesized via free radical polymerization reaction and modified with different alkyl dihalides of variable chain lengths such as 1,2-dibromoethane (1,2-BE) and 1,4-dibromobutane (1,4-BB) to obtain polymeric ionic liquid The chem. structure of synthesized p(1-VIm) macroporous hydrogel was confirmed by Fourier transform IR spectroscopy (FT-IR) and SEM. P(1-VIm)-Ag, 1,2-BE-p(1-VIm)-Ag, and 1,4-BB-p(1-VIm)-Ag were prepared by reducing Ag(CH3COO) metal salts loaded into p(1-VIm) hydrogels and then reducing with NaBH4. Metal nanoparticles embedded p(1-VIm)-Ag were visualized by transmission electron microscopy. The metal content of all composites was estimated via at. absorption spectroscopy, and its amount was 4.44 mmol/g hydrogel, 5.44 mmol/g hydrogel, and 8.39 mmol/g hydrogel, for p(1-VIm), 1,2-BE-p(1-VIm), and 1,4-BB-p(1-VIm), resp. According to the results, metal content of quaternized hydrogels is higher than nonquaternized. P(1-VIm)-Ag, 1,2-BE-p(1-VIm)-Ag, and 1,4-BB-p(1-VIm)-Ag composites were used as catalyst in the aerobic oxidation of olefins by emphasizing the effects of different parameters such as temperature, substituent effect, etc. Olefin oxidation reaction was carried out in higher oxidation conversion by 1,2-BE-p(1-VIm)-Ag and 1,4-BB-p(1-VIm)-Ag than p(VIm)-Ag, due to high hydrophobicity of quaternized composites. The prepared porous hydrogel composites were also used as catalyst in H2 generation from hydrolysis of sodium borohydride (NaBH4). The activation energies, enthalpy, and entropy for NaBH4 hydrolysis catalyzed by composites were determined According to the results, p(VIm)-Ag showed higher catalytic activity. Low performance of 1,4-BB-p(1-VIm)-Ag than 1,2-BE-p(1-VIm)-Ag and p(1-VIm)-Ag is due to high hydrophobicity of this hydrogel than the other catalytic systems whiles reaction medium is water. Furthermore, the p(1-VIm), 1,2-BE-p(1-VIm), and 1,4-BB-p(1-VIm) were utilized in the adsorption of oxo-anions such as Cr2O7-2, CrO4-2 and MnO4-. Between hydrogels, 1,4-BB-p(1-VIm) has better performance than 1,2-BE-p(1-VIm) and p(1-VIm). Because of that, ion absorption capacity is increased with an increase in the number of carbon atoms in the chain of the alkylation agents. In addition, pH dependency of adsorbents was investigated and p(VIm) showed high pH dependency. Indeed, hydrophilic/hydrophobic character and permanent pos. charges of Q-p(VIm) hydrogels made them independent of the solution pH. Finally, the catalyst was easily recovered from the reaction medium, and it could be reused for other four runs without significant loss of activity. Durability of catalyst structure without leaching confirmed by FT-IR spectra and at. absorption spectroscopy, resp.

The article 《Synthesis, characterization, and fabrication of silver nanoparticles in 1-vinyl imidazole-based hydrogels and their use in olefin oxidation, hydrogen generation, and oxo-anion adsorption》 also mentions many details about this compound(110-52-1)HPLC of Formula: 110-52-1, you can pay attention to it, because details determine success or failure

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 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, Journal of Molecular Structure called Pure rotational spectrum and structural determination of 1,1-difluoro-1-silacyclopentane, Author is Moon, Nicole T.; Marshall, Frank E.; McFadden, Thomas M. C.; Ocola, Esther J.; Laane, Jaan; Guirgis, Gamil A.; Grubbs, Garry S. II, which mentions a compound: 110-52-1, SMILESS is BrCCCCBr, Molecular C4H8Br2, Formula: C4H8Br2.

The ground state, pure rotational spectrum of 1,1-difluoro-1-silacyclopentane has been studied using chirped-pulse, Fourier transform microwave (CP-FTMW) spectroscopy and observed in the 6-20.3 GHz region of the electromagnetic spectrum. This spectrum was acquired leveraging the deep averaging capability of the technique. The parent species, 13C, 29Si, and 30Si singly substituted isotopologues were observed in natural abundance and are reported. Only one conformer, the C2 conformer (half-chair), was observed This is confirmed with a determined CCCC dihedral angle of -48.1(11)°. The spectrum is comprised of entirely a-type transitions in accordance with quantum chem. calculations Multiple split transitions are present in the spectrum which have been attributed to a ring-twisting of the carbon atoms attached to the silicon atom in the ring. This motion has the carbons crossing the a-axis in the bc-plane leading to an inversion potential. Potential energy surfaces for the ring-twisting motion were undertaken and the exptl. determined energy level difference observed in comparison to these surfaces is reasonable. A Kraitchman anal. of the exptl. determined, singly substituted isotopologues is in agreement with the optimized, twisted (nonplanar) equilibrium structure. This structure has been compared to other similar silicon-containing ring mols. using second moment arguments and these comparisons are discussed.

The article 《Pure rotational spectrum and structural determination of 1,1-difluoro-1-silacyclopentane》 also mentions many details about this compound(110-52-1)Formula: C4H8Br2, you can pay attention to it, because details determine success or failure

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

Electric Literature of C4H8Br2. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: 1,4-Dibromobutane, is researched, Molecular C4H8Br2, CAS is 110-52-1, about Pd nanoparticles supported on MOF/ionic liquid system: a heterogeneous catalyst for the C-O bond formation via Ullmann-type reaction. Author is Askari, Saeed; Khodaei, Mohammad Mehdi; Jafarzadeh, Mohammad.

Abstract: Palladium nanoparticles (NPs) are deposited on the supported ionic liquid (IL). The IL is initially supported on zirconium metal-organic framework (i.e., UiO-66-NH2), and subsequently modified with guanidine. It is proposed that the presence of amine groups in the guanidine can efficiently stabilize the NPs. The composite system, UiO-66-NH2-ILPF6–guanidine-Pd NPs, is used for catalyzing a C-O coupling Ullmann reaction. This heterogeneous catalyst exhibited excellent activity for the reaction between Ph halides and phenol derivatives in the absence of an addnl. base, which typically used for deprotonation of phenols. In other words, the counter-anion of the IL acts as a base for this reaction. The catalyst is capable to recover and reuse several times with reasonable activity.

After consulting a lot of data, we found that this compound(110-52-1)Electric Literature of C4H8Br2 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

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 110-52-1, is researched, Molecular C4H8Br2, about Stereoelectronic Evaluation of Pyrazole- and Indazole-Derived N-Heterocyclic Carbenes, the main research direction is pyrazolium bromide preparation metalation silver transmetalation palladium; indazolium bromide preparation metalation silver transmetalation palladium; crystal structure pyrazolium bromide triflate pyrazolinylidene indazolinylidene palladium carbene; mol structure pyrazolium bromide triflate pyrazolinylidene indazolinylidene palladium carbene.Safety of 1,4-Dibromobutane.

Pyrazolin- and indazolin-3-ylidenes belong to a class of less-explored and nonclassical NHCs. A small library of these ligands with subtle variations is introduced, and their electronic properties were assessed by NMR spectroscopy using the HEP values and the 1J(C-H) coupling constants of the azolium salts. An intermethod comparison revealed that 13C NMR chem. shifts demonstrated higher sensitivity toward discrete structural modifications, providing finer differentiation within and across pyrazole- and indazole-derived NHCs. Also, slight variations in steric bulk (%Vbur) can be achieved by the choice of substituents and benzannulation. The straightforward preparation of air-stable Pd complexes holds promise for a wider applicability of these strongly donating NHCs in organometallic chem.

After consulting a lot of data, we found that this compound(110-52-1)Safety of 1,4-Dibromobutane 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

Recommanded Product: 110-52-1. 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: 1,4-Dibromobutane, is researched, Molecular C4H8Br2, CAS is 110-52-1, about Multicomponent click polymerization for the synthesis of coumarin containing 1,4-polytriazoles and their application as dye adsorbent. Author is Bhaumick, Prabhas; Choudhury, Lokman H..

The synthesis of heterocycle-based polymers have remained an important area of research in polymer chem. Herein we report a one-pot synthesis of a set of novel coumarin containing regioselective 1,4-polytriazols by multicomponent click polymerization using Cs2CO3 as a base and copper(I) acetate as a catalyst in DMF medium. In this one-pot process, O-alkylation followed by a three-component click reaction between the coumarin-linked dialkyne, sodium azide and alkyl/benzyl dibromides provide novel polymers having coumarin-triazole-linker (C-T-L) units. Ten novel polymers have been synthesized with high mol. weights (Mw = 20,080-46,340 g/mol) and very good yields (83-93%). All the polymers were well characterized by IR, NMR, and GPC. The dye removal capacities of these polymers were evaluated for methylene blue (MB), rhodamine B (RB), methyl orange (MO), and congo red (CR). Polymers P1, P2, and P3 showed very high affinity towards methylene blue dye and among them, P2 showed the highest dye removal efficiency (971 mg/g) for MB. The reusability of P2 was checked and found excellent removal efficiency (RE = 96%) up to the eighth cycle.

Although many compounds look similar to this compound(110-52-1)Recommanded Product: 110-52-1, numerous studies have shown that this compound(SMILES:BrCCCCBr), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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

Aknin, Karen; Bontemps, Alexis; Farce, Amaury; Merlet, Eric; Belmont, Philippe; Helissey, Philippe; Chavatte, Philippe; Sari, Marie-Agnes; Giorgi-Renault, Sylviane; Desbene-Finck, Stephanie published the article 《Polycyclic nitrogen heterocycles as potential thymidine phosphorylase inhibitors: synthesis, biological evaluation, and molecular docking study》. Keywords: pyrimidoquinolinedione preparation thymidine phosphorylase inhibitor SAR mol docking; dioxopyrimidinylalkyl pyrroloquinolinedione preparation thymidine phosphorylase inhibitor SAR mol docking; pyrrolopyridopyrimidinetetraone preparation thymidine phosphorylase inhibitor SAR mol docking; Thymidine phosphorylase inhibitor; molecular docking; multicomponent reactions; pyrido[2,3-d]pyrimidinedione; pyrimido[4,5-b]quinoline-2,4-dione.They researched the compound: 1,4-Dibromobutane( cas:110-52-1 ).Synthetic Route of C4H8Br2. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:110-52-1) here.

New polycyclic heterocycles I [R1 = H, Me, 3,4,5-trimethoxyphenyl; R2 = 7-Me, 8-methoxy, 8-phenoxy, etc.], II [n = 4, 6; R3 = Br, methyl], III [R4 = H, Cl, Br, etc.], IV [n = 1, 2; R5 = cyclohexyl, Ph, 3-pyridinyl, etc.] were synthesized and evaluated as potential inhibitors of thymidine phosphorylase (TP). Inspired by the pharmacophoric pyrimidinedione core of the natural substrate, four series were designed in order to interact with large empty pockets of the active site: pyrimidoquinoline-2,4-diones (I), pyrimidinedione linked to a pyrroloquinoline-1,3-diones (II and III), the polycyclic heterocycle were replaced by a pyrimidopyridopyrrolidinetetraone (IV). In each series, the tricyclic nitrogen heterocyclic moiety were synthesized by a one-pot multicomponent reaction. Compared to 7-deazaxanthine used as control I [8-methoxy, 8-chloro, 5-methyl-8-methoxy], II [n = 1; R5 = phenyl] , and the open intermediate V showed modest to good activities. A kinetic study confirmed that the most active compounds I [8-methoxy, 5-methyl-8-methoxy] were competitive inhibitors. Mol. docking anal. confirmed the interaction of these new compounds I, II, III, IV, V at the active binding site of TP and highlighted a plausible specific interaction in a pocket that had not yet been explored.

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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

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 110-52-1, is researched, Molecular C4H8Br2, about Rongalite-induced transition-metal and hydride-free reductive aldol reaction: a rapid access to 3,3′-disubstituted oxindoles and its mechanistic studies, the main research direction is oxindole preparation; isatin rongalite transition metal hydride free reductive aldol reaction.Recommanded Product: 110-52-1.

A transition-metal and hydride-free reductive aldol reaction has been developed for the synthesis of biol. active 3,3′-disubstituted oxindoles from isatin derivatives using rongalite. In this protocol, rongalite plays a dual role as a hydride-free reducing agent and a C1 unit donor. This transition metal-free method enables the synthesis of a wide range of 3-hydroxy-3-hydroxymethyloxindoles and 3-amino-3-hydroxymethyloxindoles with 79-96% yields. One-pot reductive hydroxymethylation, inexpensive rongalite (ca. $0.03/1 g), mild reaction conditions and short reaction time are some of the key features of this synthetic method. This protocol is also applicable to gram scale synthesis.

In some applications, this compound(110-52-1)Recommanded Product: 110-52-1 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

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

Application of 110-52-1. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 1,4-Dibromobutane, is researched, Molecular C4H8Br2, CAS is 110-52-1, about Two new anion exchange membranes based on poly(bis-arylimidazolium) ionenes blend polybenzimidazole. Author is Yu, Na; Dong, Jianhao; Wang, Tingting; Jin, Yaping; Tang, Weiqin; Yang, Jingshuai.

The development of polymer membranes with excellent alk. stability and high hydroxide conductivity is a huge challenge to fuel cells. Herein, two blend membranes based on poly(bis-arylimidazolium)s (i.e. Ppbim and Ptpim) and polybenzimidazole (PBI) are prepared and used as anion exchange membranes. Ppbim and Ptpim ionenes are synthesized from bis-imidazole compounds (i.e. pbim and tpim) and α,α’-dibromo-p-xylene via the Menshutkin reaction, while pbim and tpim are synthesized from 2-phenylbenzimidazole (or 2,4,5-triphenylimidazole) with 1,4-dibromobutane through the nucleophilic substitution reaction. The physicochem. properties such as water uptake, ion exchange capacity, swelling, tensile strength and conductivity can be adjusted by changing the molar ratio of pbim (or tpim) to PBI in the blend membranes. Comparing with Ppbim, Ptpim containing bulky tri-Ph groups exhibits better alk. stability due to the steric hindrance effect of tri-Ph groups. The tech. feasibility of the Ptpim-51%PBI membrane for the anion exchange membrane fuel cell is demonstrated by the polarization curves. This work provides a straightforward method to synthesize water-insoluble ether-free polymers with dicationic groups in the polymer repeat unit.

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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