The origin of a common compound about 1762-34-1

Compound(1762-34-1)Quality Control of 5,5′-Dimethyl-2,2′-bipyridine received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

Quality Control of 5,5′-Dimethyl-2,2′-bipyridine. 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: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about A binuclear iron(III) complex of 5,5′-dimethyl-2,2′-bipyridine as cytotoxic agent. Author is Kondori, Tahere; Akbarzadeh-T, Niloufar; Ghaznavi, Habib; Karimi, Zeinab; Shahraki, Jafar; Sheervalilou, Roghayeh; Shahraki, Omolbanin.

The binuclear iron(III) complex (1), namely, {[Fe(5,5′-dmbpy)2(OH2)]2(O)}(NO3)4 with a distorted octahedral coordination, formed by four nitrogen and two oxygen atoms, was previously reported by our team. In this study the DNA-binding and cytotoxicity evaluation for target complex were studied. The results indicated strong cytotoxicity activity against A549 cells comparable to cisplatin values. The binding interaction between complex 1 and FS-DNA was investigated by UV-Vis, fluorescence spectroscopy, and gel electrophoresis at physiol. pH (7.2). The DNA binding investigation has shown groove binding interactions with complex 1, therefore the hydrogen binding plays an important role in the interaction of DNA with complex 1. The calculated thermodn. parameters (ΔH°, ΔS° and ΔG°) show that hydrogen bonding and Vander-Waals forces have an important function in Fe(III) complex-DNA interaction. Moreover, DNA cleavage was studied using agarose gel electrophoresis. Viscosity measurements illustrated that relative viscosity of DNA was unchanged with the adding concentrations of Fe(III) complex. Mol. docking simulation results confirmed the spectroscopic and viscosity titration outcomes.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Why Are Children Getting Addicted To 1762-34-1

Compound(1762-34-1)Quality Control of 5,5′-Dimethyl-2,2′-bipyridine received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

Quality Control of 5,5′-Dimethyl-2,2′-bipyridine. 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: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about Controlling the Synthesis of Metal-Organic Framework UiO-67 by Tuning Its Kinetic Driving Force. Author is Kaur, Gurpreet; Oeien-Oedegaard, Sigurd; Lazzarini, Andrea; Chavan, Sachin Maruti; Bordiga, Silvia; Lillerud, Karl Petter; Olsbye, Unni.

The successful synthesis of metal-organic framework (MOF) compounds relies on an intricate interplay between the components of the synthesis liquor at the given synthesis conditions. The interdependence of modulator, linker, and solvent amounts in the synthesis of the Zr-based MOF, UiO-67, is explored. Probably control of linker vacancy defects in UiO-67 is feasible by tuning the ratios of these components, and such control derives from recognizing the kinetic driving forces during MOF crystal growth. Linker vacancy defects (and modulator mols. occupying linker sites) can be reduced by limiting the solvent amount to maintain a saturated concentration of linker throughout the synthesis. The method enables formation of UiO-67 with an ideal 1:1 ratio between Zr and the 4,4′-biphenyldicarboxylic acid linker, without surplus linker in the mother liquor or addnl. post-synthetic steps, and reduces the amount of DMF solvent to <20% the amount in previously reported procedures. Compound(1762-34-1)Quality Control of 5,5′-Dimethyl-2,2′-bipyridine received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Extended knowledge of 1762-34-1

Compound(1762-34-1)COA of Formula: C12H12N2 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

Zhu, Yao; He, Yong-Qin; Tian, Wan-Fa; Wang, Mei; Zhou, Zhao-Zhao; Song, Xian-Rong; Ding, Hai-Xin; Xiao, Qiang published the article 《Dual Cobalt and Photoredox Catalysis Enabled Redox-Neutral Annulation of 2-Propynolphenols》. Keywords: hydroxymethyl benzofuran preparation; phenol hydroxyalkynyl redox neutral heterocyclization organophotoredox cobalt catalyst.They researched the compound: 5,5′-Dimethyl-2,2′-bipyridine( cas:1762-34-1 ).COA of Formula: C12H12N2. 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:1762-34-1) here.

A hydroxyl-assisted, organophotoredox/cobalt dual catalyzed annulation of 2-propynolphenols I [R1 = H, R2 = H, F, Cl, Br, MeO2C, Me; R1 = Cl, R2 = H; R1 = R2 = F; R3 = R4 = Me, Ph, 4-FC6H4, 3-F3CC6H4, etc.; R3 = Ph, R4 = Me, 4-ClC6H4, 2-FC6H4, 4-F3CC6H4, 2-thienyl, etc.; R3 = 4-FC6H4, R4 = 4-MeOC6H4; R3R4 = (CH2)5] to form 2-(hydroxymethyl)benzo[b]furans II has been developed by employing 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN) as photosensitizer and CoCl2(PPh3)2/5,5′-dimethyl-2,2′-bipyridine as cobalt catalytic precursor. Various substrates and functional groups were tolerated. The practical applications of this reaction were further demonstrated by enlarged gram-scale and various derivations for complex heterocycles. Primary mechanistic studies suggested the involvement of cobalt-hydride mediated hydrogen atom transfer (HAT) process.

Compound(1762-34-1)COA of Formula: C12H12N2 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Simple exploration of 1762-34-1

Compound(1762-34-1)Name: 5,5′-Dimethyl-2,2′-bipyridine received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

Kondori, Tahere; Akbarzadeh-T, Niloufar; Ghaznavi, Habib; Karimi, Zeinab; Sheervalilou, Roghayeh; Dusek, Michal; Eigner, Vaclav; Shahraki, Omolbanin published the article 《Structure analysis and biological functionalities of a nickel(II) complex and its sonochemically synthesized nano form: in vitro anti-proliferation, DNA binding, antibacterial and molecular docking study》. Keywords: nickel methylbipyridine thiocyanate complex preparation crystal structure; DNA binding nickel methylbipyridine thiocyanate complex nanoparticle; antibacterial anticancer antioxidant activity nickel methylbipyridine thiocyanate complex.They researched the compound: 5,5′-Dimethyl-2,2′-bipyridine( cas:1762-34-1 ).Name: 5,5′-Dimethyl-2,2′-bipyridine. 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:1762-34-1) here.

A compound of {[Ni(5,5′-Dimethyl-2,2′-bipyridine)3](SCN)2}2(a) was synthesized and characterized by FTIR, UV-visible spectroscopy, elemental anal., luminescence and x-ray crystallog. The single crystals were obtained by slow crystallization from a methanol solution The complex is composed of nickel cation chelated by three neutral bipyridine ligands and two (SCN-) ions outside the coordination sphere. The nano form of the synthesized complex (b) was prepared by a sonochem. process and confirmed with XRD, SEM and FTIR. The average size of the particles was 37 nm from SEM. Thermodn. parameters (ΔH°, ΔS° and ΔG°) calculated from FS-DNA interaction of complexes showed that hydrogen bonding and van der Waals interactions have an essential function in the interaction of DNA-Ni(II) complex, and the interaction mode is groove binding. Viscosity measurement illustrated that relative viscosity of DNA remained unchanged with the adding concentrations of complexes. CD spectra showed that the structure of DNA was changed. The antibacterial properties were investigated in vitro against standard Gram-pos. and Gram-neg. bacterial strains. The results of antibacterial tests showed that (a) was a stronger antibacterial agent than the free ligand, and that the antibacterial effect of (b) was stronger than the one of (a). The cytotoxicity activity experiments against MCF-7, KB and A549 cells revealed low to moderate antiproliferative activity of the complex (b) against cancer cells. The mol. docking results exhibited groove mode of binding, confirming previously obtained data from spectroscopy, viscometry and CD.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Some scientific research about 1762-34-1

Compound(1762-34-1)COA of Formula: C12H12N2 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

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: 1762-34-1, is researched, Molecular C12H12N2, about Spectroscopic, structural and DFT studies of luminescent Pt(II) and Ag(I) complexes with an asymmetric 2,2′-bipyridine chelating ligand, the main research direction is carbomethoxybipyridine preparation platinum silver complexation; crystal mol structure methylcarbomethoxybipyridine platinum silver complex; DFT luminescent platinum silver methylcarbomethoxybipyridine asym bipyridine chelating ligand.COA of Formula: C12H12N2.

A new unsym. substituted 2,2′-bipyridine ligand, 5-methyl-5′-carbomethoxy-2,2′-bipyridine (L) was isolated from the dry distillation of the copper(II) complex, mono-aqua-bis(trans-5-methyl-pyridine-2-carboxylato-N,O)copper(II). The ligand was fully characterized. The spectroscopic and single-crystal x-ray diffraction (SCXRD) studies of the coordination compounds of the ligand with platinum(II) and silver(I); cis-Pt(L)Cl2 (1) and [Ag(L)2]PF6 (2), resp. are reported. In 1, the Pt center coordinates to tertiary N atoms of the ligand and two chloride ions to form a neutral square-planar coordination sphere, while in 2, the Ag(I) center is coordinated by two ligands through N atoms to generate a cationic flattened tetrahedron geometry in which two mean planes intersect each other at 50.93°. The pyridine rings are nearly coplanar as revealed by the torsion angle of N2-C7-C6-N1 1.32(5)°. In both complexes, L acts as a chelating ligand through pyridyl N atoms. In 1, the mol. units are stacked in a head-to-tail fashion with a Pt···Pt separation of 3.5 Å. Supramol. self-assembly of the mol. units by extensive intermol. contacts through C-H···Cl and C-H···O between the adjacent units results in an infinite two-dimensional flattened-out herringbone structure in the crystalline state. In 2, the mol. units are interconnected with each other by C-H···O contacts between the adjacent units running parallel to each other. Both complexes are fluorescent in solution and have emission maxima in the UV-Vis regions, which is a very important property for optoelectronic applications. DFT (d. functional theory) and TD-DFT (time-dependent-DFT) calculations were performed at B3LYP/6-311+G(d,p)/LANL2DZ level to explore structural, electronic, and spectroscopic properties to compare with the exptl. results. The MOs were carried out with DFT at the same level.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Brief introduction of 1762-34-1

Compound(1762-34-1)Name: 5,5′-Dimethyl-2,2′-bipyridine received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 5,5′-Dimethyl-2,2′-bipyridine( cas:1762-34-1 ) is researched.Name: 5,5′-Dimethyl-2,2′-bipyridine.Goncalves, Guilherme R.; de Carvalho, Alexandre B.; Honorato, Joao; Oliveira, Katia M.; Correa, Rodrigo S. published the article 《A new polymorph of six-coordinated bis(5,5′-dimethyl-2,2′-bipyridine) nitratocopper(II) nitrate and its DNA interactions》 about this compound( cas:1762-34-1 ) in Journal of Molecular Structure. Keywords: copper methylbipyridine preparation crystal structure DNA binding Hirshfeld surface. Let’s learn more about this compound (cas:1762-34-1).

Here, the authors present a new polymorph of the [Cu(5mebipy)(NO3)]NO3 complex (1, Form II), where 5mebipy means 5,5′-dimethyl-2,2′-bipyridine. 1 Was characterized by spectroscopic techniques and single-crystal x-ray diffraction. Form II presents a six-coordinated structure, meanwhile the Form I, previously reported, is five-coordinated with the nitrate ligand as monodentate. The mol. structures of both crystalline forms were compared based on intramol. aspects using Kleywegt’s anal. and the intermol. contacts evaluated by Hirshfeld surface studies. Also, the interaction of [Cu(5mebipy)(NO3)]+ with CT-DNA was carried out using viscosity and spectrophotometric titrations, exhibiting a binding constant of 2.57 × 104 M – 1. This study contributes to explore the intra and intermol. details of the new polymorph of [Cu(5mebipy)(NO3)]NO3 and its capability to interacts with CT-DNA.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Chemical Research in 1762-34-1

Compound(1762-34-1)Product Details of 1762-34-1 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

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: 1762-34-1, is researched, SMILESS is CC1=CN=C(C=C1)C1=NC=C(C)C=C1, Molecular C12H12N2Journal, Journal of Molecular Liquids called Dimeric imidazolium ionic liquids connected by bipyridiyl as a corrosion inhibitor for N80 carbon steel in HCl, Author is Zhang, Juantao; Kong, Minjian; Feng, Jiangtao; Yin, Chengxian; Li, Danping; Fan, Lei; Chen, Qibin; Liu, Honglai, the main research direction is dimeric imidazolium ionic liquid bipyridiyl carbon steel corrosion inhibitor.Product Details of 1762-34-1.

A new type of the dimeric imidazolium-type amphiphile, BDBCmIB (m = 1, 4 and 8), was synthesized using the bipyridiyl as the spacer, and its inhibition performance and mechanism for the corrosion of N80 carbon steel in 1.0 mol·L-1 HCl were evaluated using chem. and electrochem. measurements, surface analyses and d. functional theory (DFT) calculations Results show that the inhibition efficiency of BDBCmIBs increases with their concentrations and the length of tail chains. BDBC8IB exhibits the best inhibition performance among them and its inhibition efficiency almost exceeds 90% in a wide concentration range from 1.0 × 10-6 to 5.0 × 10-4 mol·L-1 at 25.0 °C, which attains the maximum over 95% at 5.0 × 10-4 mol·L-1. Moreover, three BDBCmIBs all display the high inhibition efficiency at 5.0 × 10-4 mol·L-1, nearly exceeding 90%, in the temperature range from 25.0 to 55.0 °C. As a mixed-type inhibitor, BDBCmIBs can retard both cathodic hydrogen evolution and anodic metal dissolution processes, since BDBCmIB mols. bear the imidazolium-based heterocycle with the electron-donating ability and the bipyridine with the electron-accepting ability, thereby facilitating the formation of a protective film on the surface of N80 carbon steel via electrostatic interactions, coordinated and back-donating bonds. The adsorption of BDBCmIBs obeys the Langmuir isothermal model. Our finding demonstrates that the introduction of the bipyridiyl at the spacer does favor improving the inhibition efficiency of such dimeric imidazolium-type amphiphiles, and meanwhile, the proper increase in the number of carbon atoms in the substituents on the imidazole rings can also enhance the inhibition efficiency.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Discovery of 1762-34-1

Compound(1762-34-1)Safety of 5,5′-Dimethyl-2,2′-bipyridine received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

Safety of 5,5′-Dimethyl-2,2′-bipyridine. 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: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about The laser-induced potential jump: A method for rapid electron injection into oxidoreductase enzymes. Author is Sanchez, Monica L. K.; Konecny, Sara E.; Narehood, Sarah M.; Reijerse, Edward J.; Lubitz, Wolfgang; Birrell, James A.; Dyer, R. Brian.

Oxidoreductase enzymes often perform technol. useful chem. transformations using abundant metal cofactors with high efficiency under ambient conditions. The understanding of the catalytic mechanism of these enzymes is, however, highly dependent on the availability of well-characterized and optimized time-resolved anal. techniques. We have developed an approach for rapidly injecting electrons into a catalytic system using a photoactivated nanomaterial in combination with a range of redox mediators to produce a potential jump in solution, which then initiates turnover via electron transfer (ET) to the catalyst. The ET events at the nanomaterial-mediator-catalyst interfaces are, however, highly sensitive to the exptl. conditions such as photon flux, relative concentrations of system components, and pH. Here, we present a systematic optimization of these exptl. parameters for a specific catalytic system, namely, [FeFe] hydrogenase from Chlamydomonas reinhardtii (CrHydA1). The developed strategies can, however, be applied in the study of a wide variety of oxidoreductase enzymes. Our potential jump system consists of CdSe/CdS core-shell nanorods as a photosensitizer and a series of substituted bipyridinium salts as mediators with redox potentials in the range from -550 to -670 mV (vs. SHE). With these components, we screened the effect of pH, mediator concentration, protein concentration, photosensitizer concentration, and photon flux on steady-state photoreduction and hydrogen production as well as ET and potential jump efficiency. By manipulating these exptl. conditions, we show the potential of simple modifications to improve the tunability of the potential jump for application to study oxidoreductases.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Decrypt The Mystery Of 1762-34-1

Compound(1762-34-1)HPLC of Formula: 1762-34-1 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

Zou, Guo-Dong; Gong, Liao-Kuo; Liu, Li; Zhang, Qian; Zhao, Xiang-Hua published the article 《Two low-dimensional transition metal coordination polymers constructed from thiophene-2,5-dicarboxylic acid and N/O-donor ligands: Syntheses, structures and magnetic property》. Keywords: thiophenedicarboxylic acid transition metal coordination polymer preparation structure magnetic.They researched the compound: 5,5′-Dimethyl-2,2′-bipyridine( cas:1762-34-1 ).HPLC of Formula: 1762-34-1. 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:1762-34-1) here.

Two low-dimensional transition metal coordination polymers (CPs), namely, Co(TDC)(Hdmea)2 (1), [Mn(TDC)(5,5′-dmbpy)(H2O)]n (2) (H2TDC = thiophene-2,5-dicarboxylic acid, Hdmea = N,N-dimethylethanolamine, 5,5′-dmbpy = 5,5′-dimethyl-2,2′-dipyridyl) have been synthesized and characterized. Compound 1 which is the first coordination compound containing the H2TDC and chelating Hdmea ligands so far features an isolated structure containing the centrosym. dinuclear [Co(TDC)(Hdmea)2]2 unit. Notably, the imidazole ligand as one of the reactants is not incorporated into the final structure of compound 1, but it is important to obtain the single crystals suitable for single-crystal X-ray diffraction anal. Compound 2 possesses a one-dimensional (1D) zigzag chain based on the [Mn(TDC)(5,5′-dmbpy)(H2O)] building unit. In addition, the magnetic property of compound 2 is investigated.

Compound(1762-34-1)HPLC of Formula: 1762-34-1 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Machine Learning in Chemistry about 1762-34-1

Compound(1762-34-1)Safety of 5,5′-Dimethyl-2,2′-bipyridine received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(5,5′-Dimethyl-2,2′-bipyridine), if you are interested, you can check out my other related articles.

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: 5,5′-Dimethyl-2,2′-bipyridine, is researched, Molecular C12H12N2, CAS is 1762-34-1, about Isoxazole Strategy for the Synthesis of 2,2′-Bipyridine Ligands: Symmetrical and Unsymmetrical 6,6′-Binicotinates, 2,2′-Bipyridine-5-carboxylates, and Their Metal Complexes.Safety of 5,5′-Dimethyl-2,2′-bipyridine.

An effective strategy was developed for the synthesis of new 2,2′-bipyridine ligands, sym. and unsym. 6,6′-binicotinates, and 2,2′-bipyridine-5-carboxylates, from 4-propargylisoxazoles. The synthesis of sym. 2,2′-disubstituted 6,6′-binicotinates was achieved using the Eglinton reaction of 5-methoxy-4-(prop-2-yn-1-yl)isoxazoles with Cu(OAc)2, followed by Fe(NTf2)2/Au(NTf2)tBuXPhos-catalyzed isomerization of the so-formed mixture of isoxazole/azirine-substituted biacetylenic intermediates. Unsym. 2,2′-disubstituted 6,6′-binicotinates were prepared via a copper-free Sonogashira coupling of 5-methoxy-4-(prop-2-yn-1-yl)isoxazoles with 6-bromonicotinates to give Me 6-(3-(5-methoxyisoxazol-4-yl)prop-1-ynyl)pyridine-3-carboxylates, followed by a transformation of the propargylisoxazole moiety of the adduct into the pyridine fragment under Fe(II)/Au(I) relay catalysis conditions. 6-(Pyrid-2-yl)nicotinates were synthesized by a Stille-type coupling of 2-(tributylstannyl)pyridine with 6-bromonicotinates. Several cyclopalladated complexes of a new series of 6,6′-binicotinates and 2,2′-bipyridine-5-carboxylates and the homoleptic Cu(I) complex were synthesized in high yields.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem