Cas: 2425-77-6 was involved in experiment | Applied Energy 2020

2-Hexyl-1-decanol(cas: 2425-77-6) is a fatty acid that is found in the essential oils of plants and has been shown to have fungicidal properties.Application In Synthesis of 2-Hexyl-1-decanol It has also been shown to inhibit the growth of Candida glabrata when used as a cationic surfactant.

Seshasayee, Mahadevan Subramanya;Savage, Phillip E. published 《Oil from plastic via hydrothermal liquefaction: Production and characterization》 in 2020. The article was appeared in 《Applied Energy》. They have made some progress in their research.Application In Synthesis of 2-Hexyl-1-decanol The article mentions the following:

We determined the effect of batch holding time (0.5 h, 1 h) and temperature (350-450°C) on the yield, composition, and quality of oil formed from the hydrothermal treatment of polypropylene (PP), polystyrene (PS), polycarbonate (PC), and polyethylene terephthalate (PET). The highest oil yields for each material ranged from just 16 wt% for PET to 86 wt% for polystyrene. The depolymerization of plastics to produce oil occurs fastest in the supercritical water regime (T > 400°C). The higher heating value (HHV) of the oil from PP and PS (44-45 MJ/kg) is comparable to that of gasoline (HHV ∼ 43.4 MJ/kg). The oil from PC and PET had lower heating values but further treatment to remove oxygen atoms would increase the energy d. Increasing the hydrothermal reaction severity (longer times, higher supercritical temperatures) reduces oil yields but increases heating values. Increasing temperature causes more aromatization in the oil from PP and PS and promotes dehydration reactions during hydrothermal treatment of PET and PC. The oil from PC contained bisphenol-A as a major product. Obtaining such monomers from hydrothermal treatment would provide a revenue stream in addition to oil and thereby improve the process economics. And 2-Hexyl-1-decanol (cas: 2425-77-6) was used in the research process.

2-Hexyl-1-decanol(cas: 2425-77-6) is a fatty acid that is found in the essential oils of plants and has been shown to have fungicidal properties.Application In Synthesis of 2-Hexyl-1-decanol It has also been shown to inhibit the growth of Candida glabrata when used as a cationic surfactant.

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New progress of cas: 140-66-9 | Science of the Total Environment 2022

4-tert-Octylphenol(cas: 140-66-9) is a common environmental pollutant showing weak estrogenic effects.Related Products of 140-66-9 It has been shown to cause harm to vertebrate male reproductive systems.

Han, Yu;Hu, Li-Xin;Liu, Ting;Liu, Jing;Wang, Yu-Qing;Zhao, Jia-Hui;Liu, You-Sheng;Zhao, Jian-Liang;Ying, Guang-Guo published 《Non-target, suspect and target screening of chemicals of emerging concern in landfill leachates and groundwater in Guangzhou, South China》. The research results were published in《Science of the Total Environment》 in 2022.Related Products of 140-66-9 The article conveys some information:

Landfill sites have been regarded as a significant source of chems. of emerging concern (CECs) in groundwater. However, our understanding about the compositions of CECs in landfill leachate and adjacent groundwater is still very limited. Here we investigated the CECs in landfill leachates and groundwater of Guangzhou in South China by target, suspect and non-target anal. using high-resolution mass spectrometry (HRMS). A variety of CECs (n = 242), including pharmaceuticals (n = 64), pharmaceutical intermediates (n = 18), personal care products (n = 9), food additives (n = 18), industrial chems. (n = 82, e.g., flame retardants, plasticizers, antioxidants and catalysts), pesticides (n = 26), transformation products (n = 8) and other organic compounds (n = 17) were (tentatively) identified by non-target and suspect screening. 142 CECs were quantitated with target anal., and among them 37, 24 and 27 CECs were detected resp. in the raw leachate (272-1780μg/L), treated leachate (0.25-0.81μg/L) and groundwater (0.10-53.7μg/L). The CECs in the raw leachates were efficiently removed with the removal efficiencies greater than 88.7%. Acesulfame, bisphenol F and ketoprofen were the most abundant compounds in both treated leachate and groundwater. The CECs in groundwater was found most likely to be originated from the landfill sites. Our results highlight the importance of non-target screening in identifying CECs, and reveal the contamination risk of groundwater by landfill leachate. To complete the study, the researchers used 4-tert-Octylphenol (cas: 140-66-9) .

4-tert-Octylphenol(cas: 140-66-9) is a common environmental pollutant showing weak estrogenic effects.Related Products of 140-66-9 It has been shown to cause harm to vertebrate male reproductive systems.

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Guo, Pengfei et al. published new experimental results with the assistance of cas: 579-43-1

rel-(1R,2S)-1,2-Diphenylethane-1,2-diol(cas: 579-43-1 Synthetic Route of C14H14O2) has been used in the preparation of trans-methyl meso-hydrobenzoin phosphite.

Guo, Pengfei;Liao, Shengyun;Wang, Shun;Shi, Jing;Tong, Xinli published 《Highly efficient and selectivity-controllable aerobic oxidative cleavage of C-C bond over heterogeneous Fe-based catalysts》. The research results were published in《Journal of Catalysis》 in 2021.Synthetic Route of C14H14O2 The article conveys some information:

A base-free selectivity-controllable aerobic oxidative cleavage of C-C bond with heterogeneous Fe-based catalysts (FexOy-N@C3N4) was developed. In the presence of oxygen, 1,2-diols were selectively transformed to the corresponding aldehyde, while the Me esters were orientedly produced from 1,2-diones in methanol medium.rel-(1R,2S)-1,2-Diphenylethane-1,2-diol (cas: 579-43-1) were involved in the experimental procedure.

rel-(1R,2S)-1,2-Diphenylethane-1,2-diol(cas: 579-43-1 Synthetic Route of C14H14O2) has been used in the preparation of trans-methyl meso-hydrobenzoin phosphite.

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Cas: 2425-77-6 was involved in experiment | Journal of Biobased Materials and Bioenergy 2021

2-Hexyl-1-decanol(cas: 2425-77-6) is a fatty acid that is found in the essential oils of plants and has been shown to have fungicidal properties.Recommanded Product: 2425-77-6 It has also been shown to inhibit the growth of Candida glabrata when used as a cationic surfactant.

Wang, Yali;Yang, Lu;Zhang, Ke;Chen, Xiaoxiang;Wang, Hangyu;Cheng, Ping;Wang, Jinhui published 《Untargeted metabolomics analysis of different grape varieties and different parts of wine grape using gas chromatography and mass spectrometry technique》. The research results were published in《Journal of Biobased Materials and Bioenergy》 in 2021.Recommanded Product: 2425-77-6 The article conveys some information:

Natural active compounds are an important key to the development and utilization of functional foods and medicine. In this study, the chem. diversity and varietal differences of wine grape were studied by using the untargeted metabolomics method based on gas chromatog.-mass spectrometry (GC-MS), and the secondary metabolites of different cultivars and different parts were analyzed. A GC-MS-based metabolomic approach and chemometrics tools was used to identify potential active compounds in Vitis vinifera. The results showed that the content of active compounds in red wine varieties was higher than that in white wine varieties, and the content of active ingredients in grape seeds was significantly higher than that in fruits. In conclusion, this study analyzed the metabolite composition and differentiation of different wine grape fruits in Turpan as a whole, and is expected to lay a foundation for the study of wine grape and to provide a theor. basis for development and utilization of the Dietary supplement and medicine on them. The experimental procedure involved many compounds, such as 2-Hexyl-1-decanol (cas: 2425-77-6) .

2-Hexyl-1-decanol(cas: 2425-77-6) is a fatty acid that is found in the essential oils of plants and has been shown to have fungicidal properties.Recommanded Product: 2425-77-6 It has also been shown to inhibit the growth of Candida glabrata when used as a cationic surfactant.

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Cas: 579-43-1 | Mecozzi, Francesco et al. made new progress in 2017

Desymmetrization of rel-(1R,2S)-1,2-Diphenylethane-1,2-diol(cas:579-43-1 Recommanded Product: 579-43-1) using chiral phosphine catalyst has been reported. Conversion of meso-hydrobenzoin to trans-stillbene oxide by treatment with an aryl sulfonyl chloride and aqueous sodium hydroxide has been reported.

Recommanded Product: 579-43-1In 2017, Mecozzi, Francesco;Dong, Jia Jia;Saisaha, Pattama;Browne, Wesley R. published 《Oxidation of Vicinal Diols to α-Hydroxy Ketones with H2O2 and a Simple Manganese Catalyst》. 《European Journal of Organic Chemistry》published the findings. The article contains the following contents:

α-Hydroxy ketones are valuable synthons in organic chem. Here we show that oxidation of vic-diols to α-hydroxy ketones with H2O2 can be achieved with an in situ prepared catalyst based on manganese salts and pyridine-2-carboxylic acid. Furthermore the same catalyst is effective in alkene epoxidation, and it is shown that alkene oxidation with the MnII catalyst and H2O2 followed by Lewis acid ring opening of the epoxide and subsequent oxidation of the alkene to α-hydroxy ketones can be achieved under mild (ambient) conditions. To complete the study, the researchers used rel-(1R,2S)-1,2-Diphenylethane-1,2-diol (cas: 579-43-1) .

Desymmetrization of rel-(1R,2S)-1,2-Diphenylethane-1,2-diol(cas:579-43-1 Recommanded Product: 579-43-1) using chiral phosphine catalyst has been reported. Conversion of meso-hydrobenzoin to trans-stillbene oxide by treatment with an aryl sulfonyl chloride and aqueous sodium hydroxide has been reported.

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Application of cas: 599-64-4 | Xiong, Xiaodong et al. published an article in 2020

4-(2-Phenylpropan-2-yl)phenol(cas:599-64-4) is a natural product found in Panax ginseng.Electric Literature of C15H16O 4-(2-Phenylpropan-2-yl)phenol is a useful reagent for preparing and characterizing aromatic polyphosphonates as high refractive index polymers.

Electric Literature of C15H16O《Access to Chiral Bisphenol Ligands (BPOL) through Desymmetrizing Asymmetric Ortho-Selective Halogenation》 was published in 2020. The authors were Xiong, Xiaodong;Zheng, Tianyu;Wang, Xinyan;Tse, Ying-Lung Steve;Yeung, Ying-Yeung, and the article was included in《Chem》. The author mentioned the following in the article:

A facile strategy to prepare potent chiral bisphenols (BPOLs) through the desymmetrizing asym. ortho-halogenation was described. Both theor. and exptl. studies were conducted in order to shed light on the mechanistic picture. The halogen handles in the BPOL products were manipulated to yield unsym. chiral BPOL ligands, which were potential privileged catalyst scaffolds and was applied in other asym. catalytic reactions.4-(2-Phenylpropan-2-yl)phenol (cas: 599-64-4) were involved in the experimental procedure.

4-(2-Phenylpropan-2-yl)phenol(cas:599-64-4) is a natural product found in Panax ginseng.Electric Literature of C15H16O 4-(2-Phenylpropan-2-yl)phenol is a useful reagent for preparing and characterizing aromatic polyphosphonates as high refractive index polymers.

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Learn more about cas: 599-64-4 | Environmental Science & Technology 2020

4-(2-Phenylpropan-2-yl)phenol(cas:599-64-4) is a natural product found in Panax ginseng.HPLC of Formula: 599-64-4 4-(2-Phenylpropan-2-yl)phenol is a useful reagent for preparing and characterizing aromatic polyphosphonates as high refractive index polymers.

HPLC of Formula: 599-64-4In 2020, Medvedev, Alexander V.;Medvedeva, Lyubov A.;Martsen, Elena;Moeser, Mathew;Gorman, Kristen L.;Lin, Benjamin;Blackwell, Brett;Villeneuve, Daniel L.;Houck, Keith A.;Crofton, Kevin M.;Makarov, Sergei S. published 《Harmonized Cross-Species Assessment of Endocrine and Metabolic Disruptors by Ecotox FACTORIAL Assay》. 《Environmental Science & Technology》published the findings. The article contains the following contents:

Environmental pollution is a threat to humans and wildlife species. Of particular concern are endocrine disrupting chems. (EDCs). An important target of EDCs is nuclear receptors (NRs) that control endocrine and metabolic responses through transcriptional regulation. Owing in part to structural differences of NRs, adverse effects of EDCs vary significantly among species. Here, we describe a multiplexed reporter assay (the Ecotox FACTORIAL) enabling parallel assessment of compounds’ effects on estrogen, androgen, thyroid, and PPARγ receptors of representative mammals, birds, reptiles, amphibians, and fish. The Ecotox FACTORIAL is a single-well assay comprising a set of species-specific, one-hybrid GAL4-NR reporter constructs transiently transfected into test cells. To harmonize cross-species assessments, we used a combination of two approaches. First, we used the same type of test cells for all reporters; second, we implemented a parallel detection of reporter RNAs. The assay demonstrated excellent quality, reproducibility, and insignificant intra-assay variability. Importantly, the EC50 values for NR ligands were consistent with those reported for conventional assays. Using the assay allowed ranking the hazard potential of environmental pollutants (e.g., bisphenols, polycyclic aromatic hydrocarbons, and synthetic progestins) across species. Furthermore, the assay permitted detecting taxa-specific effects of surface water samples. Therefore, the Ecotox FACTORIAL enables harmonized assessment of the endocrine and metabolic disrupting activity of chems. and surface water in humans as well as in wildlife species. And 4-(2-Phenylpropan-2-yl)phenol (cas: 599-64-4) was used in the research process.

4-(2-Phenylpropan-2-yl)phenol(cas:599-64-4) is a natural product found in Panax ginseng.HPLC of Formula: 599-64-4 4-(2-Phenylpropan-2-yl)phenol is a useful reagent for preparing and characterizing aromatic polyphosphonates as high refractive index polymers.

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ACS Energy Letters | Cas: 2425-77-6 was involved in experiment

2-Hexyl-1-decanol(cas: 2425-77-6) has been shown to inhibit the growth of b16 mouse melanoma cells, suggesting it may be useful for treating skin cancer.Safety of 2-Hexyl-1-decanol This fatty acid also has transport properties and can form hydrogen bonds with other molecules.

Safety of 2-Hexyl-1-decanol《Bithieno[3,4-c]pyrrole-4,6-dione-Mediated Crystallinity in Large-Bandgap Polymer Donors Directs Charge Transportation and Recombination in Efficient Nonfullerene Polymer Solar Cells》 was published in 2020. The authors were Zhao, Jiaji;Li, Qingduan;Liu, Shengjian;Cao, Zhixiong;Jiao, Xuechen;Cai, Yue-Peng;Huang, Fei, and the article was included in《ACS Energy Letters》. The author mentioned the following in the article:

Solution-processed nonfullerene bulk-heterojunction (BHJ) polymer solar cells (PSCs), which are composed of polymer donors and organic acceptors, are proven to manifest promising performance and long-term stability. In this concise contribution, bithieno[3,4-c]pyrrole-4,6-dione (BiTPD), which is a TPD derivative but presents a large planar structure and strong electron-withdrawing ability, was used to construct a large-bandgap polymer donor PBiTPD. Results show that the polymer donor PBiTPD realized power conversion efficiency (PCE) as high as 14.2% in fullerene-free BHJ solar cells. Larger ionization potential value, more favorable face-on backbone orientation, and stronger crystallinity were concurrently obtained in PBiTPD. Correspondingly, improved and more balanced charge transportation; less nongeminate and trap-assisted recombination losses; and thus high fill factor (FF) of 67%, short-circuit c.d. (Jsc) of 25.6 mA·cm-2, and high open-circuit voltage (Voc) of 0.83 V were concurrently achieved in PBiTPD-based devices. PBiTPD does clear the way for a novel and promising class of large-bandgap polymer donor candidates.2-Hexyl-1-decanol (cas: 2425-77-6) were involved in the experimental procedure.

2-Hexyl-1-decanol(cas: 2425-77-6) has been shown to inhibit the growth of b16 mouse melanoma cells, suggesting it may be useful for treating skin cancer.Safety of 2-Hexyl-1-decanol This fatty acid also has transport properties and can form hydrogen bonds with other molecules.

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Explore more uses of cas: 579-43-1 | ACS Central Science

rel-(1R,2S)-1,2-Diphenylethane-1,2-diol(cas: 579-43-1 Related Products of 579-43-1) has been used in the preparation of trans-methyl meso-hydrobenzoin phosphite.

Yang, Lu;Wenzel, Thomas;Williamson, R. Thomas;Christensen, Melodie;Schafer, Wes;Welch, Christopher J. published 《Expedited Selection of NMR Chiral Solvating Agents for Determination of Enantiopurity》. The research results were published in《ACS Central Science》 in 2016.Related Products of 579-43-1 The article conveys some information:

The use of NMR chiral solvating agents (CSAs) for the anal. of enantiopurity was known for decades, but was supplanted in recent years by chromatog. enantioseparation technol. While chromatog. methods for the anal. of enantiopurity are now commonplace and easy to implement, there are still individual compounds and entire classes of analytes where enantioseparation can prove extremely difficult, notably, compounds that are chiral by virtue of very subtle differences such as isotopic substitution or small differences in alkyl chain length. NMR anal. using CSAs can often be useful for such problems, but the traditional approach to selection of an appropriate CSA and the development of an NMR-based anal. method often involves a trial-and-error approach that can be relatively slow and tedious. The authors describe a high-throughput experimentation approach to the selection of NMR CSAs that employs automation-enabled screening of prepared libraries of CSAs in a systematic fashion. This approach affords excellent results for a standard set of enantioenriched compounds, providing a valuable comparative data set for the effectiveness of CSAs for different classes of compounds The technique was successfully applied to challenging pharmaceutical development problems that are not amenable to chromatog. solutions Overall, this methodol. provides a rapid and powerful approach for studying enantiopurity that compliments and augments conventional chromatog. approaches.rel-(1R,2S)-1,2-Diphenylethane-1,2-diol (cas: 579-43-1) were involved in the experimental procedure.

rel-(1R,2S)-1,2-Diphenylethane-1,2-diol(cas: 579-43-1 Related Products of 579-43-1) has been used in the preparation of trans-methyl meso-hydrobenzoin phosphite.

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Plant Molecular Biology | Cas: 2425-77-6 was involved in experiment

2-Hexyl-1-decanol(cas: 2425-77-6) may be employed as an organic solvent to study the extraction of non-polar acidic drugs from human plasma by parallel artificial liquid membrane extraction (PALME). Quality Control of 2-Hexyl-1-decanol

Hu, Shuangling;Chen, Qinghua;Guo, Fei;Wang, Mingle;Zhao, Hua;Wang, Yu;Ni, Dejiang;Wang, Pu published 《(Z)-3-Hexen-1-ol accumulation enhances hyperosmotic stress tolerance in Camellia sinensis》 in 2020. The article was appeared in 《Plant Molecular Biology》. They have made some progress in their research.Quality Control of 2-Hexyl-1-decanol The article mentions the following:

Volatile components in fresh leaves are involved in the regulation of many stress responses, such as insect damage, fungal infection, high temperature Here, we found that 7-day hyperosmotic treatment specifically led to the accumulation of (Z)-3-hexen-1-ol, (E)-2-hexenal and Me salicylate. (Z)-3-hexen-1-ol pretreatment dramatically enhanced the hyperosmotic stress tolerance of tea plants and decreased stomatal conductance, whereas (E)-2-hexenal and Me salicylate pretreatments did not exhibit. qRT-PCR anal. revealed that exogenous ABA induced the expressions of related enzyme genes, and (Z)-3-hexen-1-ol could up-regulate the expressions of many DREB and RD genes. Moreover, exogenous (Z)-3-hexen-1-ol tremendously induced the expressions of specific LOX and ADH genes within 24 h. Taken together, hyperosmotic stress induced (Z)-3-hexen-1-ol accumulation in tea plant via LOX, HPL and ADH genes, (Z)-3-hexen-1-ol could dramatically enhance the hyperosmotic stress tolerance via the decrease of stomatal conductance and MDA, accumulation of ABA and proline, activation of DREB and RD gene expressions. Key message: Hyperosmotic stress induced (Z)-3-hexen-1-ol accumulation in Camellia sinensis via up-regulation of most LOX, HPL and ADH genes, while (Z)-3-hexen-1-ol could dramatically enhance the hyperosmotic stress tolerance via the decrease of stomatal conductance, accumulation of proline, activation of DREB and RD gene expressions, and probably pos. feedback regulation of LOXs and ADHs. To complete the study, the researchers used 2-Hexyl-1-decanol (cas: 2425-77-6) .

2-Hexyl-1-decanol(cas: 2425-77-6) may be employed as an organic solvent to study the extraction of non-polar acidic drugs from human plasma by parallel artificial liquid membrane extraction (PALME). Quality Control of 2-Hexyl-1-decanol

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