Application of cas: 140-66-9 | Lee, Seok-Hee et al. published an article in 2022

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

Lee, Seok-Hee;Seo, Huiwon;Seo, Hyeyeong;Lazari, Maria;D’Agostino, Martin;Byrd, Nick;Yoon, Kyong Sup;Lee, Hee-Seok;Park, Yooheon published 《An In vitro dimerization assay for the adverse outcome pathway approach in risk assessment of human estrogen receptor α-mediated endocrine-disrupting chemicals》. The research results were published in《Chemosphere》 in 2022.Product Details of 140-66-9 The article conveys some information:

The adverse outcome pathway (AOP) has been recently proposed as an effective framework for chem. risk assessment. The AOP framework offers the advantage of effectively integrating individual in vitro studies and in silico prediction models. Thus, the development of an effective testing method to measure key events caused by chems. is essential for chem. risk assessment through a fully developed AOP framework. We developed a human cell-based estrogen receptor α (ERα) dimerization assay using the bioluminescence resonance energy transfer (BRET) technique and evaluated the ERα dimerization activities of 72 chems. Fifty-one chems. were identified to mediate dimerization of ERα, and the BRET-based ERα dimerization assay could effectively measure the events that mediated dimerization of ERα by the estrogenic chems. These results were compared with the results of pre-existing assay to determine whether the BRET-based ERα dimerization assay could be employed as an in vitro test method to provide scientific information for explaining key events as a part of the AOP framework. Consequently, we propose that the BRET-based ERα dimerization assay is suitable for measuring the chem.-mediated dimerization of ERα, a key event in the AOP framework for cellular-level risk assessment of estrogenic chems.4-tert-Octylphenol (cas: 140-66-9) were involved in the experimental procedure.

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

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Fluid Phase Equilibria | Cas: 80-46-6 was involved in experiment

4-tert-acylphenol (cas:80-46-6) contains hydroxyl group. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. Butanol, with a four-carbon chain, is moderately soluble.Electric Literature of C11H16O

Mulero, Angel;Pierantozzi, M.;Cachadina, Isidro;Di Nicola, G. published 《An Artificial Neural Network for the surface tension of alcohols》. The research results were published in《Fluid Phase Equilibria》 in 2017.Electric Literature of C11H16O The article conveys some information:

An Artificial Neural Network model is proposed for the calculation and prediction of the surface tension of alcs. A total amount of 4316 data for 147 alcs. was used for training, validating and testing the network model. After considering different architectures, the one giving better results includes an input layer that uses four independent variables (temperature, critical point temperature, critical d., and radius of gyration), two hidden layers with 21 neurons each one, and one neuron in the output layer was found to give the best results. Overall mean absolute percentage deviation of 1.04% was found, whereas models based on corresponding-states principle give mean deviations higher than 11.3%. The experimental procedure involved many compounds, such as 4-tert-Amylphenol (cas: 80-46-6) .

4-tert-acylphenol (cas:80-46-6) contains hydroxyl group. Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. Butanol, with a four-carbon chain, is moderately soluble.Electric Literature of C11H16O

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Sun, Jinyan et al. published new experimental results with the assistance of cas: 119-47-1

Recommanded Product: 119-47-12,2′-Methylenebis(4-methyl-6-tert-butylphenol)(CAS: 119-47-1) is a natural product found in Streptomyces and Aspergillus fumigatus .

Recommanded Product: 119-47-1《Preparation of a Coal-Based MoS2/SiO2/GO Composite Catalyst and Its Performance in the Photocatalytic Degradation of Wastewater and Hydrogen Production》 was published in 2022. The authors were Sun, Jinyan;Maimaiti, Halidan;Zhai, Peishuai;Zhang, Haizheng;Feng, Lirong;Bao, Jianzhao;Zhao, Xuwei, and the article was included in《Langmuir》. The author mentioned the following in the article:

Photocatalytic degradation of wastewater and the simultaneous production of hydrogen (H2) is a green and efficient method to solve energy and environmental problems. In this paper, coal-based SiO2/GO with a stable structure was prepared by a modified Hummers oxidation method, and then, a lotus-shaped composite photocatalyst, MoS2/SiO2/GO, was prepared by in situ loading of flower cluster MoS2 from sodium molybdate reduction onto SiO2/GO. Its photocatalytic degradation of wastewater and H2 production properties were investigated while characterizing the material structure. The results show that SiO2/GO as a carrier not only ensures adequate dispersion of MoS2 but also enhances the visible-light response of the composite catalyst. In addition, it can also hinder the recombination of photogenerated electrons and holes in MoS2 and act as an electron transport channel in composite catalysts. MoS2/SiO2/GO exhibits much higher photocatalytic degradation of wastewater and H2 production capacity than MoS2: after 180 min of reaction, the CODcr removal of wastewater increased from 45.6% for MoS2 to 84.2% for MoS2/SiO2/GO and the H2 yield reached 233.4μmol. The goal of degrading wastewater while producing H2 more economically has been tentatively achieved, although not to the extent required for industrialization. The experimental procedure involved many compounds, such as 2,2-Methylenebis(6-tert-butyl-p-cresol) (cas: 119-47-1) .

Recommanded Product: 119-47-12,2′-Methylenebis(4-methyl-6-tert-butylphenol)(CAS: 119-47-1) is a natural product found in Streptomyces and Aspergillus fumigatus .

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Cas: 110-03-2 was involved in experiment | Nature Communications 2021

2,5-Dimethyl-2,5-hexanediol(cas:110-03-2) on heteropoly acid catalyzed dehydration yields cyclic ethers via stereospecific intramolecular SN2 mechanism. It reacts with nitriles in concentrated sulfuric acid to yield Δ1-pyrrolines.Recommanded Product: 110-03-2

Recommanded Product: 110-03-2《Selective deoxygenative alkylation of alcohols via photocatalytic domino radical fragmentations》 was published in 2021. The authors were Guo, Hong-Mei;Wu, Xuesong, and the article was included in《Nature Communications》. The author mentioned the following in the article:

A one-pot strategy for deoxygenative Giese reaction of alcs. with electron-deficient alkenes, by using xanthate salts as alc.-activating groups for radical generation under visible-light photoredox conditions in the presence of triphenylphosphine were reported. The convenient generation of xanthate salts and high reactivity of sequential C-S/C-O bond homolytic cleavage enable efficient deoxygenation of primary, secondary and tertiary alcs. with diverse functionality and structure to generate the corresponding alkyl radicals, including Me radical. Moreover, chemoselective radical monodeoxygenation of diols was achieved via selective formation of xanthate salts.2,5-Dimethyl-2,5-hexanediol (cas: 110-03-2) were involved in the experimental procedure.

2,5-Dimethyl-2,5-hexanediol(cas:110-03-2) on heteropoly acid catalyzed dehydration yields cyclic ethers via stereospecific intramolecular SN2 mechanism. It reacts with nitriles in concentrated sulfuric acid to yield Δ1-pyrrolines.Recommanded Product: 110-03-2

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Cas: 140-66-9 | Li, Shuyingpublished an article in 2021

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

Li, Shuying;Hu, Tiantian;Bertotto, Luisa Becker;Jiang, Yao;Gui, Wenjun;Schlenk, Daniel published 《Pesticide and Surfactant Mixtures Alter Sexual Differentiation in Japanese Medaka (Oryzias latipes)》 in 2021. The article was appeared in 《ACS ES&T Water》. They have made some progress in their research.Product Details of 140-66-9 The article mentions the following:

Effects-directed analyses of water extracts from the San Francisco Bay Delta of California using estrogenic activity indicated that the pesticides, bifenthrin, and diuron, as well as alkylphenol surfactants, were observed in active fractions. To determine whether the estrogenic activity of the mixture had any impacts on sexual development, Japanese medaka (Oryzias latipes) embryos were exposed to an ambient concentration of the compounds, individually and as mixtures, using components of the US Environmental Protection Agency (USEPA), Endocrine Disruptor Screening Program, and Organization for Economic Co-operation and Development (OECD) assay. In medaka exposed to diuron, or surfactants alone, the percentages of phenotypic females were 88.9 ± 19.2% and 66.4 ± 3.8%, resp. When diuron was combined with surfactants, 93.3 ± 5.8% of the animals were female. To evaluate whether phenotypic females were changed from genetically male animals, the expression of the male-specific gene (DMY) was measured in animals following treatment. Treatments with ambient concentrations of surfactants and diuron had animals with higher percentages (78 ± 19%) of phenotypic females that were derived from genotypic males. Our results demonstrated that mixtures of pesticides and surfactants may alter sexual development after embryonic exposure in fish.4-tert-Octylphenol (cas: 140-66-9) were involved in the experimental procedure.

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

Reference:
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Application of cas: 599-64-4 | Tang, Xiaowen et al. published an article in 2021

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

Tang, Xiaowen;Luo, Xiang;Su, Qiong;Wei, Gaofei;Meng, Shan-Shui;Chan, Albert S. C. published 《Chemoselective dual functionalization of phenols via relay catalysis of borane with different forms》 in 2021. The article was appeared in 《CCS Chemistry》. They have made some progress in their research.Application In Synthesis of 4-(2-Phenylpropan-2-yl)phenol The article mentions the following:

A highly efficient and chemoselective dual functionalization of unprotected phenols with α- or β- hydroxyl acids was presented. A variety of valuable benzofuranones and dihydrocoumarins were delivered in moderate to high yields. D. functional theory (DFT) calculations and control experiments indicated that an untypical Friedel-Crafts alkylation and the subsequent lactonization were catalyzed by the Lewis acid form and the Bronsted acid form of borane, resp. Gram-scale experiments and late-stage functionalization of complex mols. were performed to highlight the utility of this reaction. 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.Application In Synthesis of 4-(2-Phenylpropan-2-yl)phenol 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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Cas: 148-51-6 was involved in experiment | Journal of Biological Chemistry 1985

5-(hydroxymethyl)-2,4-dimethylpyridin-3-ol hydrochloride(cas:148-51-6 Category: alcohols-buliding-blocks) is a vitamin B6 antimetabolite with diverse biological activities. It inhibits transport of pyridoxine , pyridoxal, and pyridoxamine in and reduces growth of S. carlsbergensis cells. DOP inhibits sphingosine-1-phosphate (S1P) lyase and reduces cyclic stretch-induced apoptosis in alveolar epithelial MLE-12 cells.

Category: alcohols-buliding-blocksIn 1985, Benecky, Michael J.;Copeland, Robert A.;Hays, Thomas R.;Lobenstine, Eric W.;Rava, Richard P.;Pascal, Robert A. Jr.;Spiro, Thomas G. published 《Resonance Raman spectroscopy of pyridoxal Schiff bases》. 《Journal of Biological Chemistry》published the findings. The article contains the following contents:

Resonance Raman (RR) spectra are reported for amino acid and amine adducts of pyridoxal 5′-phosphate (PLP) and 5′-deoxypyridoxal (5′-dPL) in aqueous solution For the valine adducts, a detailed study was carried out on solutions at pH and pD 5, 9, and 13, values at which the pyridine and imine protons are successively ionized, and on the adducts formed from [15N]valine, α-deuterovaline, and N-methyl-PLP. Good quality spectra were obtained, despite the strong fluorescence of pyridoxal Schiff bases, by adding KI as a quencher, and by exciting the mols. on the blue side of their absorption bands: 406.7 nm (cw K+ laser) for the pH 5 and 9 species (λmax = 409 and 414 nm), and 354.7 nm (pulsed YAG laser, 3rd harmonic) for the pH 13 species (λmax = 360 nm). A prominent band at 1646 cm-1 was assigned to the imine C:N stretch via its 13 cm-1 15N shift. A 12 cm-1 downshift of the band in D2O confirmed that the Schiff base linkage is protonated at pH 9. Deprotonation at pH 13 shifted νC:N from 1646 to 1629 cm-1, values typical of conjugated Schiff bases. The strongest band in the spectrum, at 1338 cm-1, shifted to 1347 cm-1 upon pyridine protonation at pH 5, and was assigned to a ring mode with a large component of phenolate C-O stretch. A shoulder on its low-frequency side was assigned to the C4-C4′ stretch. Large enhancements of these modes could be understood qual. in terms of the dominant resonance structures contributing to the ground and resonant excited states. A number of weaker bands were observed, and assigned to pyridine ring modes. These modes gained significantly in intensity, and the exocyclic modes diminished, when the spectra were excited at 266 nm (YAG laser, 4th harmonic) in resonance with ring-localized electronic transitions. The experimental procedure involved many compounds, such as 5-(hydroxymethyl)-2,4-dimethylpyridin-3-ol hydrochloride (cas: 148-51-6) .

5-(hydroxymethyl)-2,4-dimethylpyridin-3-ol hydrochloride(cas:148-51-6 Category: alcohols-buliding-blocks) is a vitamin B6 antimetabolite with diverse biological activities. It inhibits transport of pyridoxine , pyridoxal, and pyridoxamine in and reduces growth of S. carlsbergensis cells. DOP inhibits sphingosine-1-phosphate (S1P) lyase and reduces cyclic stretch-induced apoptosis in alveolar epithelial MLE-12 cells.

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New progress of cas: 599-64-4 | Journal of the American Chemical Society 2021

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

Liu, Xufang;Rong, Xianle;Liu, Shihan;Lan, Yu;Liu, Qiang published 《Cobalt-Catalyzed Desymmetric Isomerization of Exocyclic Olefins》. The research results were published in《Journal of the American Chemical Society》 in 2021.COA of Formula: C15H16O The article conveys some information:

Chiral cyclic olefins, 1-methylcyclohexenes, are versatile building blocks for the synthesis of pharmaceuticals and natural products. Despite the prevalence of these structural motifs, the development of efficient synthetic methods remains an unmet challenge. Herein the authors report a novel desym. isomerization of exocyclic olefins using a series of newly designed chiral cobalt catalysts, which enables a straightforward construction of chiral 1-methylcyclohexenes with diversified functionalities. The synthetic utility of this methodol. is highlighted by a concise and enantioselective synthesis of a natural product, β-bisabolene. The versatility of the reaction products is further demonstrated by multifarious derivatization. To complete the study, the researchers used 4-(2-Phenylpropan-2-yl)phenol (cas: 599-64-4) .

4-(2-Phenylpropan-2-yl)phenol(cas:599-64-4) is a natural product found in Panax ginseng.COA of Formula: 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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Cas: 2425-77-6 | Sood, Vipasha et al. made new progress in 2020

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). Name: 2-Hexyl-1-decanol

Name: 2-Hexyl-1-decanol《Plant extracts effectiveness to extend bison meat shelf life》 was published in 2020. The authors were Sood, Vipasha;Tian, Wenchao;Narvaez-Bravo, Claudia;Arntfield, Susan D.;Gonzalez, Argenis Rodas, and the article was included in《Journal of Food Science》. The author mentioned the following in the article:

The effectiveness of plant extracts (0.05% rosemary and 0.08% oregano) to extend shelf life of bison strip loin steaks in terms of color stability and consumer acceptability was studied. Steaks treated with oregano presented lower oxygen consumption, higher metmyoglobin-reducing activity (MRA), decreased lipid oxidation, and provided a stable red color with less discoloration during the retail display period than the control and rosemary treated steaks (P < 0.05). Results from consumer sensory evaluation indicated that treated steaks under study were not significantly different from the control (P > 0.05) based on palatability attributes and acceptability. However, rosemary treated steaks were more desirable and palatable than their oregano counterparts (P < 0.05). Overall, plant extracts, particularly oregano, can improve color stability of bison steaks due to its antioxidants properties and ability to increase MRA capacity in fresh bison meat without posing any neg. impact on its sensory attributes. Practical Application : This study will provide valuable information to the bison meat industry on how to offer a more consistent and acceptable product (in terms of palatability and color) to consumers using plant-based natural antioxidants, without diminishing the palatability of their products. This technol. can offer two more days of shelf life in retail overwrap packaging, consequently, opening the possibility for the bison industry to expand its market with a potential to reduce retail losses due to poor color stability and early browning (i.e., stock out, markdowns, and waste due to expired display life). And 2-Hexyl-1-decanol (cas: 2425-77-6) was used in the research process.

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). Name: 2-Hexyl-1-decanol

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Cas: 224434-01-9 | Qian, Deyun et al. made new progress in 2021

(S) – 2-amino-2 – (4-fluorophenyl) ethanol (cas: 224434-01-9) has the characteristics of alcohol. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Related Products of 224434-01-9

Related Products of 224434-01-9《Chiral Alkyl Amine Synthesis via Catalytic Enantioselective Hydroalkylation of Enecarbamates》 was published in 2021. The authors were Qian, Deyun;Bera, Srikrishna;Hu, Xile, and the article was included in《Journal of the American Chemical Society》. The author mentioned the following in the article:

A nickel-catalyzed hydroalkylation method to assemble a wide range of chiral alkyl amines from enecarbamates (N-Cbz-protected enamines) and alkyl halides with high regio- and enantioselectivity was reported. The method works for both nonactivated and activated alkyl halides and was able to produce enantiomerically enriched amines with two minimally differentiated α-alkyl substituents. The mild conditions led to high functional group tolerance, which is demonstrated in the postproduct functionalization of many natural products and drug mols., as well as the synthesis of chiral building blocks and key intermediates to bioactive compounds And (S)-2-Amino-2-(4-fluorophenyl)ethanol (cas: 224434-01-9) was used in the research process.

(S) – 2-amino-2 – (4-fluorophenyl) ethanol (cas: 224434-01-9) has the characteristics of alcohol. In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. Related Products of 224434-01-9

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