Category: 2380-78-1

Phytochemical and network-based chemotaxonomic study on Thalictrum foliolosum was written by He, Gongxiu;Tu, Xichen;Yan, Yuanfeng;Peng, Jun;Yin, Tianpeng. And the article was included in Biochemical Systematics and Ecology in 2022.Reference of 2380-78-1 The following contents are mentioned in the article:

Phytochem. investigation on the whole herbs of Thalictrum foliolosum DC. (Ranunculaceae) led to the isolation of eighteen compounds, including nine isoquinoline alkaloids (1-9) and nine nonalkaloidal constituents (10-18). Among them, compounds 11-14 and 16-18 have not been previously isolated from this genus, while compounds 1, 7, 10, and 15 have not been previously found in this species. The chemotaxonomic values of these compounds were explored by compound-species network anal. Some of the isolated compounds (1, 7, 10) showed limited distribution in the genus, which could serve as chemotaxonomic markers to facilitate species identification of T. foliolosum. This study involved multiple reactions and reactants, such as 4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1Reference of 2380-78-1).

4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Reference of 2380-78-1

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Phytochemical and chemotaxonomic study on the dried rhizome of Menispermum dauricum DC was written by Ren, Wenjing;Wu, Haoran;Tian, Zhenhua;Zhang, Wenyu;Dong, Wenliang;Jiang, Haiqiang;Liu, Yuhong. And the article was included in Biochemical Systematics and Ecology in 2021.Recommanded Product: 2380-78-1 The following contents are mentioned in the article:

An alkaloid (1), an amide (2), three lactones (3, 6 and 7), two coumarins (4-5), eight lignans (8-15), four alcs. (16-19) and three phenols (20-22) are obtained from the EtOAc soluble portion of the MeOH extract of the rhizome of Menispermum dauricum DC. The chem. structures of the compounds are determined by using spectroscopic methods and further supported by comparison with previous literatures. This is the first report that compounds 4-5, 12-17, 19 and 20-21 are obtained from the family Menispermaceae. Compounds 1-2, 6-11 and 22 are isolated for the first time from Menispermum genus. The chemotaxonomic significance of the compounds is also discussed. This study involved multiple reactions and reactants, such as 4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1Recommanded Product: 2380-78-1).

4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: 2380-78-1

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Flavonoids, stilbenoids, and phenolic derivatives from the stems of Gnetum macrostachyum (Gnetaceae) was written by Seo, Changon;Lym, Seung Ho;Jeong, Wonsik;Lee, Ji Eun;Lee, Jung A.;Ahn, Eun-Kyung;Kang, Jae-Shin;Kim, Won Hee;Choi, Chun Whan;Oh, Joa Sub;Hong, Seong Su. And the article was included in Biochemical Systematics and Ecology in 2020.Reference of 2380-78-1 The following contents are mentioned in the article:

Gnetum species have been traditionally consumed as food and used as folk medicine to treat various pathol. conditions. Ten compounds including three simple phenolic compounds (1-3), five stilbenoids (4, 5, 8-10), and two C-glycosyl flavanones (6 and 7), were isolated from the stems of Gnetum macrostachyum Hook. f. The structures of these compounds were elucidated by the anal. of spectroscopy data and their comparison with the reported values. This is the first report of the isolation of compounds 1-4 and 6-9 from G. macrostachyum. Compounds 1-3, 6, and 7 have not been previously reported from the genus Gnetum. The C-glycosyl flavanones in G. macrostachyum can be used as chemotaxonomic markers. This study involved multiple reactions and reactants, such as 4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1Reference of 2380-78-1).

4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1) belongs to ethers. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Reference of 2380-78-1

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Chemical constituents of the pericarp of Toona sinensis and their chemotaxonomic significance was written by Chen, Ying;Wang, Feng;Ji, Chaoying;Liu, Di;Liu, Xiaoxiao;Wang, Rongshen;Li, Wanzhong. And the article was included in Biochemical Systematics and Ecology in 2022.Reference of 2380-78-1 The following contents are mentioned in the article:

Phytochem. investigation of the pericarp of Toona sinensis (A. Juss.) Roem (Meliaceae) led to the isolation and identification of 33 compounds, namely, 7 apotirucallane-type triterpenoids (1-7), 2 cycloartane-type triterpenoids (8-9), 5 sterols (10-14), 2 sesquiterpenes (15-16), 2 lignans (17-18), 3 flavonoids (19-21), and 12 phenols (22-33). The chem. structures of these compounds were elucidated based on spectroscopic data and comparison with previously reported data. This is the first report of compounds 11-12, 16, 18, 23, and 31 from the family Meliaceae, compounds 13-15, 26, and 30 within the genus Toona, and compound 33 from T. sinensis. The chemotaxonomic significance of the isolated compounds is also described in this study. This study involved multiple reactions and reactants, such as 4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1Reference of 2380-78-1).

4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Reference of 2380-78-1

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Thiols Act as Methyl Traps in the Biocatalytic Demethylation of Guaiacol Derivatives was written by Pompei, Simona;Grimm, Christopher;Schiller, Christine;Schober, Lukas;Kroutil, Wolfgang. And the article was included in Angewandte Chemie, International Edition in 2021.Product Details of 2380-78-1 The following contents are mentioned in the article:

Demethylating Me Ph ethers is challenging, especially when the products are catechol derivatives prone to follow-up reactions. For biocatalytic demethylation, monooxygenases have previously been described requiring mol. oxygen which may cause oxidative side reactions. Here we show that such compounds can be demethylated anaerobically by using cobalamin-dependent methyltransferases exploiting thiols like Et 3-mercaptopropionate as a Me trap. Using just two equivalent of this reagent, a broad spectrum of substituted guaiacol derivatives were demethylated, with conversions mostly above 90%. This strategy was used to prepare the highly valuable antioxidant hydroxytyrosol on a one-gram scale in 97% isolated yield. This study involved multiple reactions and reactants, such as 4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1Product Details of 2380-78-1).

4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Product Details of 2380-78-1

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Preparation and properties of wood vinegar from pyrolysis of fir sawdust under different temperatures was written by Lu, Xincheng;Jiang, Jianchun;He, Jing;Sun, Kang;Sun, Yunjuan. And the article was included in Linchan Huaxue Yu Gongye in 2019.Safety of 4-Hydroxy-3-methoxyphenethanol The following contents are mentioned in the article:

The preparation and properties of wood vinegar obtained by pyrolysis of fir sawdust under different temperatures were studied. The results showed that the most important pyrolysis phase of fir sawdust was 150-250°C, which obtained the most of wood vinegar and organic compounds Under this pyrolysis phase, the highest yield of organic compound was phenols, and followed with acids. The relative content of organic compounds in wood vinegar was increased with the increasing of pyrolysis temperature, which is up to 48% after 150°C. The relative content for each kind of organic compounds was different under various temperature range, the highest relative content of acids was in 0-150°C, while phenols and ketones in 250-350°C, and aldehydes in 150-250°C. This study involved multiple reactions and reactants, such as 4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1Safety of 4-Hydroxy-3-methoxyphenethanol).

4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Safety of 4-Hydroxy-3-methoxyphenethanol

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Dealkylation of Lignin to Phenol via Oxidation-Hydrogenation Strategy was written by Wang, Min;Liu, Meijiang;Li, Hongji;Zhao, Zhitong;Zhang, Xiaochen;Wang, Feng. And the article was included in ACS Catalysis in 2018.Related Products of 2380-78-1 The following contents are mentioned in the article:

Lignin is a renewable and abundant aromatic polymer found in plants. We herein propose a “cutting tail” methodol. to produce phenol from lignin, which is achieved by combining Ru/CeO₂ catalyst and CuCl₂ oxidant via an oxidation-hydrogenation route. Phenol was obtained from separated poplar lignin with 13 wt % yield. Even raw biomass, such as poplar, birch, pine, peanut, bamboo willow, and straw, could be converted into phenol in 1-33 mg per g of biomass. This study involved multiple reactions and reactants, such as 4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1Related Products of 2380-78-1).

4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Related Products of 2380-78-1

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Modular and Divergent Syntheses of Protoberberine and Protonitidine Alkaloids was written by Liu, Kai;Jiang, Xuefeng. And the article was included in Organic Letters in 2021.Name: 4-Hydroxy-3-methoxyphenethanol The following contents are mentioned in the article:

A modularly convergent and divergent strategy was established for the family synthesis of both protoberberine and protonitidine alkaloids. The robust, scalable, and flexible synthetic route featured a collective preparation of protoberberine and protonitidine alkaloids from a common isoquinoline assembled from pyridyne as the key synthon, which was based on the selective N-C or C-C cyclization via distinct processes. Through the strategy, 20 protoberberine alkaloids, 5 protonitidine alkaloids, and 11 analogs with diverse substituents were comprehensively acquired. This study involved multiple reactions and reactants, such as 4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1Name: 4-Hydroxy-3-methoxyphenethanol).

4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Name: 4-Hydroxy-3-methoxyphenethanol

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A New Polyketide Antibiotic from the Marine Bacterium Streptomyces sp. PGC 32 was written by Ahmad, Shabir;Nazir, Mamona;Tousif, Muhammad Imran;Saleem, Muhammad;Mustafa, Rizwana;Khatoon, Tasneem. And the article was included in Chemistry of Natural Compounds in 2019.Formula: C9H12O3 The following contents are mentioned in the article:

A new aromatic polyketide compound, arabomycin (I), along with 3 known metabolites, was isolated from the culture broth of the marine bacterium Streptomyces sp. PGC 32. The structure of I was established through 1D and 2D NMR analyses and high-resolution mass spectrometry, and the known compounds were elucidated on the basis of ¹H and ¹³C NMR information in comparison with literature values. I displayed antibacterial action against the Gram-pos. bacteria Bacillus subtilis and Staphylococcus aureus, and Gram-neg. bacteria Escherichia coli and Enterobacter sp. This study involved multiple reactions and reactants, such as 4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1Formula: C9H12O3).

4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Formula: C9H12O3

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Identification by Inverse Virtual Screening of magnolol-based scaffold as new tankyrase-2 inhibitors was written by Di Micco, Simone;Pulvirenti, Luana;Bruno, Ines;Terracciano, Stefania;Russo, Alessandra;Vaccaro, Maria C.;Ruggiero, Dafne;Muccilli, Vera;Cardullo, Nunzio;Tringali, Corrado;Riccio, Raffaele;Bifulco, Giuseppe. And the article was included in Bioorganic & Medicinal Chemistry in 2018.Computed Properties of C9H12O3 The following contents are mentioned in the article:

The natural product magnolol (1) and a selection of its bioinspired derivatives 2-5, were investigated by Inverse Virtual Screening in order to identify putative biol. targets from a panel of 308 proteins involved in cancer processes. By this in silico anal. we selected tankyrase-2 (TNKS2), casein kinase 2 (CK2) and bromodomain 9 (Brd9) as potential targets for exptl. evaluations. The Surface Plasmon Resonance assay revealed that 3-5 present a good affinity for tankyrase-2, and, in particular, 3 showed an antiproliferative activity on A549 cells higher than the well-known tankyrase-2 inhibitor XAV939 used as reference compound This study involved multiple reactions and reactants, such as 4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1Computed Properties of C9H12O3).

4-Hydroxy-3-methoxyphenethanol (cas: 2380-78-1) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Computed Properties of C9H12O3

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