Month: February 2023

Ladder-Type P,S-Bridged trans-Stilbenes was written by Weymiens, Wannes;Zaal, Mark;Slootweg, J. Chris;Ehlers, Andreas W.;Lammertsma, Koop. And the article was included in Inorganic Chemistry in 2011.Electric Literature of C8H4Br2S This article mentions the following:

Phosphole-containing π-systems have emerged as building blocks with enormous potential as electronic materials because of the tunability of the phosphorus center. Among these, asym. P-bridged trans-stilbenes are still rare, and here an elegant and efficient synthesis toward such fluorescent mol. frameworks is described. Fine-tuning of the photophys. properties is attempted by enforcing the planarization of the phosphorus tripod and thus increasing the interaction between the phosphorus lone pair and the π-system. The electronic structure of the π-conjugated frameworks is analyzed with NMR, UV-vis and fluorescence spectroscopy, and time-dependent d. functional theory (TD-DFT) calculations In the experiment, the researchers used many compounds, for example, 2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7Electric Literature of C8H4Br2S).

2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7) belongs to benzothiophene derivatives. Benzothiophenes are valuable heterocycles that are widely used in medicines, agrochemicals, and materials science. It is found within the chemical structures of pharmaceutical drugs such as raloxifene, zileuton, and sertaconazole, and also BTCP.Electric Literature of C8H4Br2S

Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

2-(2-Thienyl)-5,6-dihydroxy-4-carboxypyrimidines as Inhibitors of the Hepatitis C Virus NS5B Polymerase: Discovery, SAR, Modeling, and Mutagenesis was written by Koch, Uwe;Attenni, Barbara;Malancona, Savina;Colarusso, Stefania;Conte, Immacolata;Di Filippo, Marcello;Harper, Steven;Pacini, Barbara;Giomini, Claudia;Thomas, Steven;Incitti, Ilario;Tomei, Licia;De Francesco, Raffaele;Altamura, Sergio;Matassa, Victor G.;Narjes, Frank. And the article was included in Journal of Medicinal Chemistry in 2006.Electric Literature of C9H5NS This article mentions the following:

Infections caused by hepatitis C virus (HCV) are a significant world health problem for which novel therapies are in urgent demand. The polymerase of HCV is responsible for the replication of viral RNA. The authors recently disclosed dihydroxypyrimidine carboxylates as novel, reversible inhibitors of the HCV NS5B polymerase. This series was further developed into 5,6-dihydroxy-2-(2-thienyl)pyrimidine-4-carboxylic acids such as (I) (EC₅₀ 9.3 μM), which now show activity in the cell-based HCV replication assay. The structure-activity relation of these inhibitors is discussed in the context of their physicochem. properties and of the polymerase crystal structure. We also report the results of mutagenesis experiments which support the proposed binding model, which involves pyrophosphate-like chelation of the active site Mg ions. In the experiment, the researchers used many compounds, for example, Benzo[b]thiophene-2-carbonitrile (cas: 55219-11-9Electric Literature of C9H5NS).

Benzo[b]thiophene-2-carbonitrile (cas: 55219-11-9) belongs to benzothiophene derivatives. Benzothiophene finds use in research as a starting material for the synthesis of larger, usually bioactive structures. Due to its aromaticity, thiophenes do not exhibit the same properties as conventional thioethers.Electric Literature of C9H5NS

Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

Design of reversible multi-electron redox systems using benzochalcogenophenes containing aryl and/or ferrocenyl fragments was written by Ogawa, Satoshi;Muraoka, Hiroki;Kikuta, Kenji;Saito, Fumihito;Sato, Ryu. And the article was included in Journal of Organometallic Chemistry in 2007.Synthetic Route of C8H4Br2S This article mentions the following:

2,3-Disubstituted benzo[b]thiophenes, 1,3-disubstituted benzo[c]thiophenes, and 1,3-disubstituted benzo[c]selenophene were systematically and selectively synthesized from benzo[b]thiophene or phthaloyl dichloride as a starting material, resp. Characterization of the mols. was performed by phys. and spectroscopic means and x-ray crystallog. analyses. The cyclic voltammograms of the chalcogenophene derivatives containing aryl fragments showed well-defined reversible both anodic and cathodic steps derived from the unusually stable 5π chalcogenophene radical cations and 7π chalcogenophene radical anions. The cyclic voltammograms of the novel chalcogenophene derivatives containing ferrocenyl fragments showed a well-defined reversible cathodic step derived from the unusually stable 7π chalcogenophene radical anions and 2 distinct reversible anodic steps derived from ferrocenium cations separated from each other by a thiophene-heterocycle. The radical character of several novel 7π chalcogenophene radical anions was measured by ESR spectroscopy. In the experiment, the researchers used many compounds, for example, 2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7Synthetic Route of C8H4Br2S).

2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7) belongs to benzothiophene derivatives. Benzothiophene is relatively a stable molecule. The core structure is a part of various pharmaceutical substances and natural products. It is also used in the manufacturing of dyes such as thioindigo.Synthetic Route of C8H4Br2S

Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

Polymerization of thiophene derivatives. IV. The formation of some 9-thia-1,2- and 9-thia-3,4-benzofluorene derivatives was written by Davies, W.;James, F. C.;Middleton, S.;Porter, Q. N.. And the article was included in Journal of the Chemical Society in 1955.COA of Formula: C8H4Br2S This article mentions the following:

The self-condensation of thianaphthene dioxide derivatives was studied. New syntheses have been developed for related polycyclic sulfones and sulfoxides. 10,11-Dihydro-9-thia-3,4-benzofluorene 9,9-dioxide (I) was heated 20 min. to yield an oil which was chromatographed on alumina with C₆H₆ and recrystallized to give blue fluorescent 9-thia-1,2-benzofluorene 9,9-dioxide (II), m. 195.5-6° (from C₆H₆). Fusion of II with KOH at 400° for 5 min. gives only a phenolic oil. Desulfurization of II occurs on refluxing 8 h. with Raney Ni in EtOH to give 2-phenylnaphthalene, m. 102-3°. II with LiAlH₄ yields 10,11-dihydro-9-thia-1,2-benzofluorene 9,9-dioxide (III), m. 157-8° (from EtOH). III with Br yields 3,4-dibromo-10,11-dihydro-9-thia-1,2-benzofluorene 9,9-dioxide (IV), m. 226-6.5°. Refluxing IV in pyridine gives II. On heating I with PCl₅, 2-chloro-9-thia-3,4-benzofluorene 9,9-dioxide (V), m. 294-5° (from MeOCH₂CH₂OH) is formed along with 1,2-dichloro-1,2,10,11-tetrahydro-9-thia-3,4-benzofluorene 9,9-dioxide (VI), m. 173.5-4°. Heating VI yields 9-thia-3,4-benzofluorene 9,9-dioxide (VII), m. 234°. Heating 3-chlorothianaphthene 1,1-dioxide gives 2,11-dichloro-10,11-dihydro-9-thia-3,4-benzofluorene 9,9-dioxide (VIII), m. 270-1° (from C₆H₆). Refluxing VIII with pyridine gives V. I with Br gives 2-bromo-9-thia-3,4-benzofluorene 9,9-dioxide (IX), m. 309-10°, and 1,2-dibromo-1,2,10,11-tetrahydro-9-thia-3,4-benzofluorene 9,9-dioxide (X), m. 185.5-6°. Refluxing X with pyridine gives VII. 3-Bromothianaphthene 1,1-dioxide is heated at 300° for 0.5 h. to give IX. 5-Bromothianaphthene in HOAc with H₂O₂ yields 5-bromothianaphthene 1,1-dioxide (XI), m. 144-4.5°. XI is refluxed for 3 h. with o-C₆H₄Cl₂ to give 2′,6-dibromo-10,11-dihydro-9-thia-3,4-benzofluorene 9,9-dioxide (XII), m. 228-9° (from EtOH). XII with Br yields 1,2,2′,6-tetrabromo-1,2,10,11-tetrahydro-9-thia-3,4-benzofluorene 9,9-dioxide (XIII), m. 239.5-40° (from C₆H₆). XIII on refluxing with pyridine gives 2′,6-dibromo-9-thia-3,4-benzofluorene 9,9-dioxide (XIV), m. 354-5° (from C₆H₆). XIV is reduced with LiAlH₄ to 9-thia-3,4-benzofluorene (XV). α-Naphthyl o-nitrophenyl sulfide, m. 152-3°, with H₂O₂ in HOAc yields α-naphthyl o-nitrophenyl sulfone (XVI), m. 128-9° (from EtOH). The isomeric β-naphthyl sulfone (XVII), m. 143.5-4°, is similarly prepared XVI in EtOH with Zn and HCl is reduced to o-aminophenyl α-naphthyl sulfone (XVIII), m. 177-8° (from EtOH). Similarly, XVII is reduced to o-aminophenyl β-naphthyl sulfone (XIX), m. 136-6.5°. Diazotization of XVIII and treatment with Cu gives II. Similar treatment of XIX followed by reduction with LiAlH₄ yields VII. o-Aminophenyl Ph sulfone with excess NaNO₂-HCl gives o-chlorophenyl Ph sulfone, m. 105-5.5°. Cyclization of o-PhC₆H₄SO₂Cl (XX) with AlCl₃ yields dibenzothiophene 5,5-dioxide, m. 229-30°. K o-α-naphthylbenzenesulfonate with PCl₅ gives o-α-naphthylbenzenesulfonyl chloride (XXI), m. 136-6.5° (from C₆H₆). XXI with AlCl₃ cyclized to VII. XX is treated with aqueous Na₂S to give o-PhC₆H₄SO₂H (XXII), m. 70-126°. XXII with SOCl₂ yields an oily sulfinyl chloride which is cyclized by AlCl₃ to dibenzothiophene 5-oxide, m. 189.5-90°. o-α-Naphthylbenzenesulfinyl chloride with AlCl₃ gives 9-thia-3,4-benzofluorene 9-oxide (XXIII), m. 147-8° (from C₆H₆-petr. ether). XXIII with SnCl₂ yields XV. XXIII is oxidized by H₂O₂ in HOAc to VII. In the experiment, the researchers used many compounds, for example, 2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7COA of Formula: C8H4Br2S).

2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7) belongs to benzothiophene derivatives. Benzothiophene finds use in research as a starting material for the synthesis of larger, usually bioactive structures. It is found within the chemical structures of pharmaceutical drugs such as raloxifene, zileuton, and sertaconazole, and also BTCP.COA of Formula: C8H4Br2S

Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

Toward Soluble 5,10-Diheterotruxenes: Synthesis and Reactivity of 5,10-Dioxatruxenes, 5,10-Dithiatruxenes, and 5,10-Diazatruxenes was written by Gorski, Krzysztof;Mech-Piskorz, Justyna;Lesniewska, Barbara;Pietraszkiewicz, Oksana;Pietraszkiewicz, Marek. And the article was included in Journal of Organic Chemistry in 2020.Formula: C8H4Br2S This article mentions the following:

The following work presents three general approaches allowing, for the first time, the synthesis of 5,10-diheterotruxene derivatives I (x = O, S, NEt) containing two identical heteroatoms, namely, oxygen OOC, nitrogen NNC, or sulfur SSC. Two of described pathways involve the photocyclization of the corresponding triene II as a key step leading to a heptacyclic aromatic system. The third approach is based on the acidic condensation between ninhydrin and benzo[b]heteroole III. Typical functionalizations of the 5,10-diheterotruxenes I core have also been presented. In addition, the article discusses the advantages and limitations of the three suggested paths for receiving specific 5,10-diheterotruxene derivatives I because the universal method suitable for obtaining mols. with any type of heteroatoms is not known so far. In the experiment, the researchers used many compounds, for example, 2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7Formula: C8H4Br2S).

2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7) belongs to benzothiophene derivatives. Functionalized benzothiophenes are important constructs found in molecules with wide ranging biological activity and in organic materials. Its aromaticity makes it relatively stable, although as a heterocycle, it has reactive sites which allow for functionalization.Formula: C8H4Br2S

Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

“Lock and Key Control” of Photochromic Reactivity by Controlling the Oxidation/Reduction State was written by Li, Xiaochuan;Ma, Yuzhen;Wang, Bingcai;Li, Gongan. And the article was included in Organic Letters in 2008.Related Products of 6287-82-7 This article mentions the following:

A photochem. active triangle terarylene was synthesized and the photochromic behavior was investigated. Its photochromic reactivity can be strongly suppressed by selected oxidization of the sulfur atoms in the mols. Reactivated photochromic reactivity was obtained by deoxidization of the S,S-dioxide moieties. The suppressed photoactivity of the oxidation state was attributed to the stronger intramol. hydrogen bonding interactions. In the experiment, the researchers used many compounds, for example, 2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7Related Products of 6287-82-7).

2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7) belongs to benzothiophene derivatives. Benzothiophene is used as starting material for the synthesis of bioactive molecules. The core structure is a part of various pharmaceutical substances and natural products. The different substitution patterns in these heterocycles offer new opportunities for drug discovery and other applications in materials science.Related Products of 6287-82-7

Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

Benzo[b]thiophene Fusion Enhances Local Borepin Aromaticity in Polycyclic Heteroaromatic Compounds was written by Messersmith, Reid E.;Yadav, Sangeeta;Siegler, Maxime A.;Ottosson, Henrik;Tovar, John D.. And the article was included in Journal of Organic Chemistry in 2017.Reference of 6287-82-7 This article mentions the following:

This report documents the synthesis, characterization, and computational evaluation of two isomeric borepin-containing polycyclic aromatics The syntheses of these two isomers involved sym. disubstituted alkynes that were reduced to Z-olefins followed by borepin formation either through an isolable stannocycle intermediate or directly from the alkene via the trapping of a transient dilithio intermediate. Comparisons of their magnetic, crystallog., and computational characterization to literature compounds gave valuable insights about the aromaticity of these sym. fused [b,f]borepins. The fusion of benzo[b]thiophene units to the central borepin cores forced a high degree of local aromaticity within the borepin moieties relative to other known borepin-based polycyclic aromatics Each isomer had unique electronic responses in the presence of fluoride anions. The exptl. data demonstrate that the local borepin rings in these two compounds have a relatively high amount of aromatic character. Results from quantum chem. calculations provide a more comprehensive understanding of local and global aromatic characters of various rings in fused ring systems built upon boron heterocycles. In the experiment, the researchers used many compounds, for example, 2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7Reference of 6287-82-7).

2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7) belongs to benzothiophene derivatives. Benzothiophene finds use in research as a starting material for the synthesis of larger, usually bioactive structures. It is found within the chemical structures of pharmaceutical drugs such as raloxifene, zileuton, sertaconazole, and also BTCP.Reference of 6287-82-7

Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

Photochromism and fluorescence properties of 1,2-bis(2-alkyl-1-benzothiophene-3-yl)perhydrocyclopentenes was written by Yamaguchi, Tadatsugu;Hosaka, Manabu;Shinohara, Keigo;Ozeki, Toru;Fukuda, Mitsuhiro;Takami, Shizuka;Ishibashi, Yukihide;Asahi, Tsuyoshi;Morimoto, Masakazu. And the article was included in Journal of Photochemistry and Photobiology, A: Chemistry in 2014.Safety of 3-Bromo-2-methylbenzo[b]thiophene This article mentions the following:

Three 1,2-bis(2-alkyl-1-benzothiophene-3-yl)perhydrocyclopentenes with different alkyl chain lengths (Me, Et, and propyl) at the reactive carbons were synthesized, and their photophys. properties were compared with those of 1,2-bis(2-alkyl-1-benzothiophene-3-yl)perfluorocyclopentenes. The structures of the perhydrocyclopentenes were analyzed by X-ray crystallog., and their cyclization/cycloreversion reaction and fluorescence quantum yields, and fluorescence lifetimes were measured by steady-state spectroscopy and the time-correlated single photon counting method, resp. From these results, we found the following three differences between perhydrocyclopentenes and perfluorocyclopentenes. (1) For the closed-ring isomers, the absorption bands of the perhydrocyclopentenes (around 450 nm) shifted to a shorter wavelength than those of the perfluorocyclopentenes (around 530 nm) because of the acceptor nature of the perfluorocyclopentene moiety. (2) The cyclization/cycloreversion quantum yields of the perhydrocyclopentenes were slightly larger than those of the perfluorocyclopentenes in hexane. (3) Interestingly, the fluorescence of both the open- and closed-ring isomers was observed only for the perhydrocyclopentenes, and the lifetimes of the closed-ring isomers were estimated to be <30 ps. In the experiment, the researchers used many compounds, for example, 3-Bromo-2-methylbenzo[b]thiophene (cas: 10243-15-9Safety of 3-Bromo-2-methylbenzo[b]thiophene).

3-Bromo-2-methylbenzo[b]thiophene (cas: 10243-15-9) belongs to benzothiophene derivatives. Benzothiophene is a fused ring compound of thiophene ring and benzene ring, which is an important class of heterocycles with advantageous structures. It is also used in the manufacturing of dyes such as thioindigo.Safety of 3-Bromo-2-methylbenzo[b]thiophene

Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

Synthesis of novel sensitizers with a linear conjugated di(1-benzothieno)[3,2-b:2′,3′-d]pyrrole unit for dye-sensitized solar cells was written by Zhang, Hai;Iqbal, Zafar;Chen, Zhen-E.;Hong, Yanping. And the article was included in Dyes and Pigments in 2019.Electric Literature of C8H4Br2S This article mentions the following:

Three novel D-π-A structural metal-free organic sensitizers (DBTP-1∼3) are designed, in which a linear planar aromatic group, the di(1-benzothieno)[3,2-b:2′,3′-d]pyrrole is first introduced as the π-bridge for dye-sensitized solar cells. Triphenylamine, 9,9-dimethyle-9H-fluorene and carbazole serve as the electron donor, resp., while cyanoacrylic acid is used as an electron acceptor and anchoring unit. The photophys., electrochem., theor. calculations have been employed to apprehend the correlation between the structures of DBTP-1∼3 and their photovoltaic performances. Further, co-adsorption studies are used to investigate the electronic recombination of the target dyes. As a result, the maximum power conversion efficiency of 6.50% (short-circuit current of 14.66 mA cm^-2, open-circuit voltage of 0.67 V, and fill factor of 66%) for the 2 mM chenodeoxycholic acid co-adsorbed device based on DBTP-1 is obtained, while without any co-adsorbent it gives efficiency of 4.55%. The standard dye N719 gives 8.54% power conversion efficiency. In the experiment, the researchers used many compounds, for example, 2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7Electric Literature of C8H4Br2S).

2,3-Dibromobenzo[b]thiophene (cas: 6287-82-7) belongs to benzothiophene derivatives. Benzothiophene is used as starting material for the synthesis of bioactive molecules. The core structure is a part of various pharmaceutical substances and natural products. It has been used as a raw material for the synthesis of biologically active structures and is found in pharmaceuticals such as leukotriene synthesis inhibitors and antifungals, as well as in many natural products.Electric Literature of C8H4Br2S

Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem

Synthesis and properties of an unsymmetrical diarylethene bearing a chlorine atom was written by Wang, Liqin;Pu, Shouzhi;Yan, Liushui;Liu, Weijun. And the article was included in Key Engineering Materials in 2011.COA of Formula: C9H7BrS This article mentions the following:

A new unsym. photochromic diarylethene 1-(2-methyl-benzothiophenyl)-2-(2-methyl-5-(4-chlorophenyl))perfluoroncyclopentene (1a), was synthesized and its optoelectronic properties, such as photochromism in solution as well as in poly(Me methacrylate) (PMMA) amorphous films and fluorescence were investigated. The photochromic reaction kinetics indicated that the cyclization process of 1a belongs to the zeroth order reaction and the cycloreversion process belongs to the first order reaction. Using diarylethene 1/PMMA film as recording medium and a linearly polarized 633 nm laser diode for recording and readout, polarization multiplexed image recording can be carried out in this film, which illustrated that the diarylethene can be potentially used as holog. optical recording medium. In the experiment, the researchers used many compounds, for example, 3-Bromo-2-methylbenzo[b]thiophene (cas: 10243-15-9COA of Formula: C9H7BrS).

3-Bromo-2-methylbenzo[b]thiophene (cas: 10243-15-9) belongs to benzothiophene derivatives. Benzothiophene is relatively a stable molecule. The electrophilic substitution of benzothiophene systems is much less regioselective than that of indoles. It has been used as a raw material for the synthesis of biologically active structures and is found in pharmaceuticals such as leukotriene synthesis inhibitors and antifungals, as well as in many natural products.COA of Formula: C9H7BrS

Referemce:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem