Tag: 100-200

Perovskite LaCo_xMn_1-xO_3-σ with Tunable Defect and Surface Structures as Cathode Catalysts for Li-O₂ Batteries was written by Li, Xudong;Qian, Zhengyi;Han, Guokang;Sun, Baoyu;Zuo, Pengjian;Du, Chunyu;Ma, Yulin;Huo, Hua;Lou, Shuaifeng;Yin, Geping. And the article was included in ACS Applied Materials & Interfaces in 2020.Name: 2,5,8,11-Tetraoxadodecane This article mentions the following:

Rechargeable lithium-oxygen batteries have shown great potential as next-generation sustainable and green energy storage systems. The bifunctional catalyst plays an important role in accelerating the cathode kinetics for practical realization of the batteries. Herein, we employ the surface structure and defect engineering to introduce surface-roughened nanolayers and oxygen vacancies on the mesoporous hollow LaCo_xMn_1-xO_3-σ perovskite catalyst by in situ cation substitution. The exptl. results show that the O₂-electrode with the LaCo_0.75Mn_0.25O_3-σ catalyst exhibits an extremely high discharge capacity of 10,301 mA h g^-1 at 200 mA g^-1 for the initial cycle and superior cycling stability under a capacity limit of 500 mA h g^-1 together with a low voltage gap of 1.12 V. Good electrochem. performance of LaCo_0.75Mn_0.25O_3-σ can be attributed to the synergistic effect of the hierarchical mesoporous hollow structure and the abundant oxygen vacancies all over the catalyst surface. We reveal that the modified surface structure can provide more accessibility of active sites to promote electrochem. reactions, and the introduced oxygen vacancy can serve as an efficient substrate for binding intermediate products and decomposition reactions of Li₂O₂ during discharge and charge processes. Our methodol. provides meaningful insights into the rational design of highly active perovskite catalysts in energy storage/conversion systems. In the experiment, the researchers used many compounds, for example, 2,5,8,11-Tetraoxadodecane (cas: 112-49-2Name: 2,5,8,11-Tetraoxadodecane).

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. But ether is more polar than alkenes. Ethyl ether is an excellent solvent for extractions and for a wide variety of chemical reactions. It is also used as a volatile starting fluid for diesel engines and gasoline engines in cold weather. Dimethyl ether is used as a spray propellant and refrigerant. Methyl t-butyl ether (MTBE) is a gasoline additive that boosts the octane number and reduces the amount of nitrogen-oxide pollutants in the exhaust. The ethers of ethylene glycol are used as solvents and plasticizers.Name: 2,5,8,11-Tetraoxadodecane

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

A mechanistic study on the biosynthetic regulation of bioactive metabolite Antroquinonol from edible and medicinal mushroom Antrodia camphorata was written by Hu, Yong-Dan;Zhang, Bo-Bo;Xu, Gan-Rong;Liao, Xiang-Ru;Cheung, Peter C. K.. And the article was included in Journal of Functional Foods in 2016.Application of 605-94-7 This article mentions the following:

Antroquinonol, an important bioactive metabolite from the edible mushroom Antrodia camphorata, was difficult to be synthesized by conventional submerged fermentation The present study revealed the mechanisms related to the stimulatory effect of coenzyme Q₀, camphorwood leach liquor and soybean oil on the biosynthesis of antroquinonol. Addition of coenzyme Q₀ could up-regulate the expression of S-adenosylmethionine synthetase, affording Me group for the biosynthesis of antroquinonol. Heat shock proteins and tricarboxylic acid cycle related proteins were found to participate in the biosynthetic pathway. Camphorwood leach liquor could provide the precursor of antroquinonol by acting as donor of quinone nucleus. Soybean oil could increase the permeability of mycelial cell membrane and the extraction efficiency for the intracellular hydrophobic antroquinonol. This study advances our understanding on how stimulatory agents can be used to regulate the biosynthesis of valuable metabolites produced from mushroom mycelia and facilitate the development of submerged fermentation for potential industrial application. In the experiment, the researchers used many compounds, for example, 2,3-Dimethoxy-5-methylcyclohexa-2,5-diene-1,4-dione (cas: 605-94-7Application of 605-94-7).

2,3-Dimethoxy-5-methylcyclohexa-2,5-diene-1,4-dione (cas: 605-94-7) belongs to ethers. The oxygen atom in ethers are more electronegative than carbon, thus the hydrogens which are alpha to the ethers are more acidic than the simple hydrocarbons. Ethers can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds.Application of 605-94-7

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Coenzyme Q₀, a novel quinone derivative of Antrodia camphorata, induces ROS-mediated cytotoxic autophagy and apoptosis against human glioblastoma cells in vitro and in vivo was written by Yang, Hsin-Ling;Tsai, Chia-Hsuan;Shrestha, Sirjana;Lee, Chuan-Chen;Liao, Jiunn-Wang;Hseu, You-Cheng. And the article was included in Food and Chemical Toxicology in 2021.COA of Formula: C9H10O4 This article mentions the following:

Coenzyme Q₀ (CoQ₀, 2,3-dimethoxy-5-methyl-1,4-benzoquinone) derived from Antrodia camphorata exerts anticancer activities against breast, melanoma, and ovarian carcinoma. Glioblastoma multiforme is a common tumor affecting the central nervous system. This study explored anticancer properties of CoQ₀ on human glioblastoma both in vitro and in vivo, and explained the mol. mechanism behind it. CoQ₀ treatment retarded the growth and suppressed colony formation in glioblastoma (U87MG and GBM8401) cells. CoQ₀ induced apoptosis by activation of caspase-3, cleavage of PARP, and dysregulation of Bax and Bcl-2 in both cell lines. Annexin V/PI staining indicated CoQ₀ mediated necrosis and apoptosis. Interestingly, AVOs were increased trough induction of autophagy by CoQ₀, LC3-II accumulation, and p62/SQSTM1 expression, leading to death mechanism. Z-VAD-FMK has no effect on CoQ₀-induced autophagy but autophagy inhibition by 3-methyladenine (3-MA)/chloroquine (CQ) led to CoQ0-induced apoptosis. N-acetylcysteine (NAC) inhibited CoQ₀-mediated ROS production and diminished CoQ₀-induced apoptotic and autophagic cell death. Further, CoQ₀ inhibited PI3K/AKT/mTOR signaling pathways. CoQ₀ reduced the tumor burden in U87MG and GBM8401 xenografted athymic nude mice and significantly modulated tumor xenograft by inducing apoptosis and autophagy. CoQ₀ generated ROS-mediated apoptotic and autophagic cell death for effective glioblastoma treatment. In the experiment, the researchers used many compounds, for example, 2,3-Dimethoxy-5-methylcyclohexa-2,5-diene-1,4-dione (cas: 605-94-7COA of Formula: C9H10O4).

2,3-Dimethoxy-5-methylcyclohexa-2,5-diene-1,4-dione (cas: 605-94-7) belongs to ethers. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil. The unique properties of ethers (i.e., that they are strongly polar, with nonbonding electron pairs but no hydroxyl group) enhance the formation and use of many reagents. For example, Grignard reagents cannot form unless an ether is present to share its lone pair of electrons with the magnesium atom. Complexation of the magnesium atom stabilizes the Grignard reagent and helps to keep it in solution.COA of Formula: C9H10O4

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

The synthesis of 1-haloalkyl-1,3,4,5-tetrahydro-2-benzoxepins was written by TenBrink, Ruth E.;McCall, John M.. And the article was included in Journal of Heterocyclic Chemistry in 1981.Category: ethers-buliding-blocks This article mentions the following:

Short, efficient routes to several 7,8-dimethoxy-1-haloalkyl-1,3,4,5-tetrahydro-2-benzoxepins were developed. These benzoxepins were prepared by the Lewis acid-catalyzed condensation of Cl(CH₂)₃CH(OEt)₂ or BrCH₂CH(OEt)₂ with 3,4-(MeO)₂C₆H₃(CH₂)₃OH. This condensation was facilitated by Me substitution on the propanol. In an alternate route, 3,4-(MeO)₂C₆H₃CH₂CH₂CO₂Et was acylated with ClCH₂CH₂COCl. The adduct was reduced with LiAlH₄. The resultant 3-[2-(3-chloro-1-hydroxypropyl)-4,5-dimethoxyphenyl]propanol was dehydrated to the corresponding tetrahydrobenzoxepin. In the experiment, the researchers used many compounds, for example, 3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3Category: ethers-buliding-blocks).

3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. But on the other hand, ethers undergo cleavage by reaction with acids. At room temperature, ethers are pleasant-smelling colourless liquids. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil.Category: ethers-buliding-blocks

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Quantitative structure activity relationship of inhibitors of glycolic acid oxidase was written by Singh, Pashupati Prasad;Kumar, Pragnesh;Marfatia, K.;Singh, Rajesh Kumar. And the article was included in Medicinal Chemistry: An Indian Journal in 2006.Electric Literature of C9H10O4 This article mentions the following:

In order to avoid trial and error method in selecting a suitable drug, QSAR methods have provided a rational basis to the design of enzyme inhibitors. 90 Derivatives of enzyme inhibitors, whose inhibitory potencies in term of PI₅₀ are reported, have been used as study material for QSAR study. These derivatives are divided into five groups: (1) substituted glycolic acids, (2) substituted oxyacetic acids, (3) substituted glyoxylic acids, (4) substituted-3-hydroxy-1H pyrrole-2,5-diones derivatives, (5) 4-heterocyclic substituted 3-hydroxy-1H-pyrrole-2,5-diones derivatives The QSAR study and MLR anal. have been collectively made, because the potency is reported in one unit and the target enzyme glycolic acid oxidase (GAO) is common to all. The study has been made with the help of seven descriptors in different combinations: (1) Heat of formation (ΔH_f), (2) HOMO energy (3) LUMO energy, (4) Absolute hardness (η) (5) Mol. weight (MW), (6) Electronegativity (χ) (7) Total energy (TE). This is perhaps for the first time when inhibitory potency has been related with quantum mech. parameters, without any significance to structure of compounds The values of descriptors have been obtained with the help of PC MODEL software using the semiempirical PM3 Hamiltonian. 32 Multi linear regression models using different combinations of descriptors have been developed using the project leader program associated with CAChe software. The predicted activity is close to the observed activity and the correlation coefficient is above 0.80. The best QSAR models are obtained by MLR anal. using the combinations, (i) heat of formation, mol. weight and electronegativity, (ii) mol. wight, total energy and electronegativity. In the experiment, the researchers used many compounds, for example, 2-(4-Methoxyphenoxy)acetic acid (cas: 1877-75-4Electric Literature of C9H10O4).

2-(4-Methoxyphenoxy)acetic acid (cas: 1877-75-4) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. But on the other hand, ethers undergo cleavage by reaction with acids. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).Electric Literature of C9H10O4

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Synthesis and cytotoxic activity of substituted hexahydro-2H-4,6-(epoxymethano)chromen-8(5H)-ones obtained from (-)-verbenone was written by Il’ina, I. V.;Pokrovsky, M. A.;Mikhalchenko, O. S.;Korchagina, D. V.;Volcho, K. P.;Pokrovsky, A. G.;Salakhutdinov, N. F.. And the article was included in Russian Chemical Bulletin in 2015.Application In Synthesis of 3-Hydroxy-5-methoxybenzaldehyde This article mentions the following:

A number of compounds with a substituted hexahydro-2H-4,6-(epoxymethano)chromen-8(5H)-one framework, I [R¹ = R⁴ = H, R² = H, OMe, R³ = OMe; R¹ = H, R² = R³ = R⁴ = OMe; R¹ = R² = R³ = OMe, R⁴ = H; R¹ = H, R² = R⁴ = OMe, R³ = OH; R¹ = R⁴ = H, R² = OH, R³ = OMe; R¹ = R⁴ = H, R² = OMe, R³ = OH], was synthesized starting from monoterpenoid (-)-verbenone and aromatic aldehydes containing methoxy and hydroxy groups. Cytotoxic activity of these compounds on human tumor cell lines was studied for the first time. Compounds containing three methoxy groups in each aromatic ring were found to be the most promising for further studies. In the experiment, the researchers used many compounds, for example, 3-Hydroxy-5-methoxybenzaldehyde (cas: 57179-35-8Application In Synthesis of 3-Hydroxy-5-methoxybenzaldehyde).

3-Hydroxy-5-methoxybenzaldehyde (cas: 57179-35-8) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. But ether is more polar than alkenes. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.Application In Synthesis of 3-Hydroxy-5-methoxybenzaldehyde

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Encapsulation effect on the in vitro bioaccessibility of sacha inchi oil (Plukenetia volubilis L.) by soft capsules composed of gelatin and cactus mucilage biopolymers was written by Otalora, Maria Carolina;Camelo, Robinson;Wilches-Torres, Andrea;Cardenas-Chaparro, Agobardo;Castano, Jovanny A. Gomez. And the article was included in Polymers (Basel, Switzerland) in 2020.Application of 111-77-3 This article mentions the following:

Sacha inchi (Plukenetia volubilis L.) seed oil is a rich source of polyunsaturated fatty acids (PUFAs) that are beneficial for human health, whose nutritional efficacy is limited because of its low water solubility and labile bioaccessibility (compositional integrity). In this work, the encapsulation effect, using blended softgels of gelatin (G) and cactus mucilage (CM) biopolymers, on the PUFAs’ bioaccessibility of P. volubilis seed oil was evaluated during in vitro simulated digestive processes (mouth, gastric, and intestinal). Gas chromatog.-mass spectrometry (GC-MS) and gas chromatog. with a flame ionization detector (GC-FID) were used for determining the chem. composition of P. volubilis seed oil both before and after in vitro digestion. The most abundant compounds in the undigested samples were α-linolenic, linoleic, and oleic acids with 59.23, 33.46, and 0.57 (g/100 g), resp. The bioaccessibility of α-linolenic, linoleic, and oleic acid was found to be 1.70%, 1.46%, and 35.8%, resp., along with the presence of some oxidation products. G/CM soft capsules are capable of limiting the in vitro bioaccessibility of PUFAs because of the low mucilage ratio in their matrix, which influences the enzymic hydrolysis of gelatin, thus increasing the release of the polyunsaturated content during the simulated digestion. In the experiment, the researchers used many compounds, for example, 2-(2-Methoxyethoxy)ethanol (cas: 111-77-3Application of 111-77-3).

2-(2-Methoxyethoxy)ethanol (cas: 111-77-3) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. But on the other hand, ethers undergo cleavage by reaction with acids. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.Application of 111-77-3

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Total synthesis of the teicoplanin aglycon was written by Boger, Dale L.;Kim, Seong Heon;Miyazaki, Susumu;Strittmatter, Harald;Weng, Jian-Hui;Mori, Yoshiki;Rogel, Olivier;Castle, Steven L.;McAtee, J. Jeffrey. And the article was included in Journal of the American Chemical Society in 2000.Related Products of 57179-35-8 This article mentions the following:

Teicoplanin is a complex of five antibiotics isolated from Actinoplanes teichomyceticus that are related to vancomycin. The first total synthesis of the teicoplanin aglycon (I) is described. Key elements of the approach include sequential DE and FG ring system introductions onto the common vancomycin/teicoplanin ABCD ring system providing a late stage divergent total synthesis of the two classes of glycopeptide antibiotics. The ring systems were introduced enlisting a nucleophilic aromatic substitution reaction of an o-fluoronitroarom. for macrocyclization and formation of the 16-membered DE diaryl ether and a macrolactamization of the N-terminus amide for closure of the 14-membered FG ring system. The teicoplanin aglycon was obtained in 48% yield identical in all respects with authentic material. In the experiment, the researchers used many compounds, for example, 3-Hydroxy-5-methoxybenzaldehyde (cas: 57179-35-8Related Products of 57179-35-8).

3-Hydroxy-5-methoxybenzaldehyde (cas: 57179-35-8) belongs to ethers. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil. At room temperature, ethers are pleasant-smelling colourless liquids. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil.Related Products of 57179-35-8

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Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

The antimicrobial activity of coenzyme Q₀ against planktonic and biofilm forms of Cronobacter sakazakii was written by Guo, Du;Wang, Shuo;Li, Jiahui;Bai, Fangting;Yang, Yanpeng;Xu, Yunfeng;Liang, Sen;Xia, Xiaodong;Wang, Xin;Shi, Chao. And the article was included in Food Microbiology in 2020.Safety of 2,3-Dimethoxy-5-methylcyclohexa-2,5-diene-1,4-dione This article mentions the following:

Coenzyme Q₀ (CoQ₀) has demonstrated antitumor, anti-inflammatory, and anti-angiogenic activities. Cronobacter sakazakii is an opportunistic foodborne pathogen associated with high mortality in neonates. In this study, the antimicrobial activity and possible antimicrobial mechanism of CoQ₀ against C. sakazakii were investigated. Moreover, the inactivation effect of CoQ₀ on C. sakazakii in biofilms was also evaluated. The min. inhibitory concentration (MIC) of CoQ₀ against C. sakazakii strains ranged from 0.1 to 0.2 mg/mL. Treatment caused cell membrane dysfunction, as evidenced by cell membrane hyperpolarization, decreased intracellular ATP concentration and cell membrane integrity, and changes in cellular morphol. CoQ₀ combined with mild heat treatment (45, 50, or 55°C) decreased the number of viable non-desiccated and desiccated C. sakazakii cells in a time- and dose-dependent manner in reconstituted infant milk. Furthermore, CoQ₀ showed effective inactivation activity against C. sakazakii in biofilms on stainless steel, reducing the number of viable cells and damaging the structure of the biofilm. These findings suggest that CoQ₀ has a strong inactivate effect on C. sakazakii and could be used in food production environments to effectively control C. sakazakii and reduce the number of illnesses associated with it. In the experiment, the researchers used many compounds, for example, 2,3-Dimethoxy-5-methylcyclohexa-2,5-diene-1,4-dione (cas: 605-94-7Safety of 2,3-Dimethoxy-5-methylcyclohexa-2,5-diene-1,4-dione).

2,3-Dimethoxy-5-methylcyclohexa-2,5-diene-1,4-dione (cas: 605-94-7) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3.Safety of 2,3-Dimethoxy-5-methylcyclohexa-2,5-diene-1,4-dione

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Host-guest complexation. 9. Macrocyclic polyethers and sulfides shaped by one rigid dinaphthyl unit and attached arms. Synthesis and survey of complexing abilities was written by Cram, Donald J.;Helgeson, Roger C.;Koga, Kenji;Kyba, Evan P.;Madan, Khorshed;Sousa, Lynn R.;Siegel, Merrell G.;Moreau, Patrice;Gokel, George W.. And the article was included in Journal of Organic Chemistry in 1978.Electric Literature of C11H16O3 This article mentions the following:

The synthesis and characterization of a stereoisomeric macrocyclic polyether, e.g., I (R, R² = H, CH₂OH, CH₂OCH₂CO₂Me, etc.; R¹ = H, Br, COMe, etc.) and polyether-polythioether hosts are described. The unshared electron pairs of the heteroatoms act as binding sites for metal or alkylammonium cations. Substituents attached at the 3,3′-positions of the 1,1′-binaphthyl unit converge on and provide addnl. shape to the space surrounding the central binding hole of the macro ring. Certain of these units terminate in functional groups that provide addnl. ligands for cationic guests, in some cases supplying counterions for the charge on the guests. Substituents attached at the 6,6′-positions of the 1,1′-binaphthyl unit diverge from the macro ring and its environment and can be used to manipulate solubility properties or to bind the hosts to solid supports. Substituents attached at the 3- or 4-positions of the 1,2-benzene units, when long enough and in the proper conformations, can curl to place addnl. binding sites on the edge of the macro ring. The maximum rotations and absolute configurations of some of the optically active hosts were determined Ring closures (6-65% yield) involved aryloxide- or arylsulfide-anion substitutions on appropriate alkyl ditosylates. In the experiment, the researchers used many compounds, for example, 3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3Electric Literature of C11H16O3).

3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3) belongs to ethers. The oxygen atom in ethers are more electronegative than carbon, thus the hydrogens which are alpha to the ethers are more acidic than the simple hydrocarbons. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).Electric Literature of C11H16O3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem