New progress of cas: 4707-47-5 | Environmental Research 2021

Methyl 2,4-dihydroxy-3,6-dimethylbenzoate(4707-47-5) is used in biological study as role of androgens in inducing distinct response of epithelial-mesenchymal transition factors in human prostate cancer cells.Safety of Methyl 2,4-dihydroxy-3,6-dimethylbenzoate

Gandhi, Arumugam Dhanesh;Miraclin, Prasanna A.;Abilash, Doraiah;Sathiyaraj, Sivaji;Velmurugan, Rajendran;Zhang, Yang;Soontarapa, Khantong;Sen, Priyankar;Sridharan, T. B. published 《Nanosilver reinforced Parmelia sulcata extract efficiently induces apoptosis and inhibits proliferative signalling in MCF-7 cells》. The research results were published in《Environmental Research》 in 2021.Safety of Methyl 2,4-dihydroxy-3,6-dimethylbenzoate The article conveys some information:

The Lichen, Parmelia sulcata synthesizes various secondary metabolites, in which phenolic based compounds received much attention due to their importance in biomedical application. Especially the phenolic compound was effective against the cancer treatment. An effective administration of such plant natural product can represent a significant conventional management of cancer in terms of chemoprevention. The nanomedicines are group of agents that selectively interfere the cancer cells which leads to reduction of side effect thereby reducing the doses. Silver nanoparticles is a promising antitumor agent, however, the conventional production of silver nanoparticles have many drawbacks which led to increase in need of eco-friendly biol. production methods. In this study, we made an attempt to synthesize a nano silver (Ps-AgNPs) from phenolic extract of lichen Parmelia sulcata extract The Ps-AgNps was applied for anticancer activity using MCF-7 cells and the effect was characterised by western blotting method. The FTIR, XRD, UV and TEM results confirms the presence of silver nanoparticles in phenolic extract of lichen Parmelia sulcata. The cytotoxicity assay shows that the Ps-AgNPs is toxic against cancer cells (MCF-7) but not to normal cells (NIH3T3), which confirm the selective induction of cell death (apoptosis) against cancer cells. The Western blot anal. also clearly indicates the down regulation of inflammatory genes (TNF-alpha and IL-6) and cell cycle genes (PCNA and Cyclin-D1) thus promoting intrinsic apoptotic pathway. The results suggest that Ps-AgNPs can effectively kill cancer cells and can be used as an alternative therapeutic agent for cancer treatment. To complete the study, the researchers used Methyl 2,4-dihydroxy-3,6-dimethylbenzoate (cas: 4707-47-5) .

Methyl 2,4-dihydroxy-3,6-dimethylbenzoate(4707-47-5) is used in biological study as role of androgens in inducing distinct response of epithelial-mesenchymal transition factors in human prostate cancer cells.Safety of Methyl 2,4-dihydroxy-3,6-dimethylbenzoate

Reference:
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Walvekar, Rashmi et al. published new experimental results with the assistance of cas: 112-62-9

Methyl oleate(cas: 112-62-9) is a fatty acid methyl ester resulting from the formal condensation of the carboxy group of oleic acid with methanol.Recommanded Product: Methyl oleate Methyl oleate(cas: 112-62-9) is an intermediate for detergents, emulsifiers, wetting agents, stabilizers, textile treatments, plasticizers for duplicating inks, rubbers, waxes etc.

Recommanded Product: Methyl oleate《Thermo-physical properties of naphthenic-palm oil methyl ester (POME) blended transformer oil》 was published in 2022. The authors were Walvekar, Rashmi;Zairin, Danial Aminin;Khalid, Mohammad;Mubarak, Nabisab Mujawar;Tcsm, Gupta, and the article was included in《Journal of Thermal Analysis and Calorimetry》. The author mentioned the following in the article:

This study aims to investigate the thermal conductivity, viscosity and thermal degradation of naphthenic-based mineral oil, palm oil Me ester (POME) and its blend. Mineral oil and POME were mixed at various mass ratios (70:30, 80:20 and 90:10) via homogenisation for 10 min at 25,000 RPM. The thermo-phys. properties of oil studied were thermal conductivity, viscosity, d., flash point and thermal degradation Results indicated enhancement in thermal conductivity with an increase in temperature The highest enhancement (0.185 W mK-1) was observed for the 70:30 blend ratio at 80°C. The viscosity decreased as temperature increased, whereby POME resulted in lower values (2.3 mPa.s) than mineral oil (4.3 mPa.s) at 80°C. D. also showed a decreasing trend with temperature with no significant difference between POME and mineral oil. However, POME (175.5°C) resulted in a higher flash point compared to mineral oil (146.5°C), resulting in the enhanced flashpoint of blend oils. Blend oil with a 70:30 ratio resulted in the highest thermal degradation of 274.56°C in the air environment. Oxidation induction time (OIT) decreased with temperature from 160-180°C where mineral oil resulted in higher induction time than POME. The results proved improvement in properties of mineral oil blend with POME, which can enhance the system performance and faster heat dissipation. And Methyl oleate (cas: 112-62-9) was used in the research process.

Methyl oleate(cas: 112-62-9) is a fatty acid methyl ester resulting from the formal condensation of the carboxy group of oleic acid with methanol.Recommanded Product: Methyl oleate Methyl oleate(cas: 112-62-9) is an intermediate for detergents, emulsifiers, wetting agents, stabilizers, textile treatments, plasticizers for duplicating inks, rubbers, waxes etc.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Cas: 129832-03-7 | Feng, Xionghanpublished an article in 2016

rel-(1R,2r,3S,4R,5s,6S)-Cyclohexane-1,2,3,4,5,6-hexayl hexakis(dihydrogen phosphate), dipotassium salt (cas:129832-03-7) is also known as Inositol hexakisphosphate. Phytic acid dipotassium salt is a potent chelator of divalent and trivalent cations, and a major determinant of zinc bioavailability.Name: rel-(1R,2r,3S,4R,5s,6S)-Cyclohexane-1,2,3,4,5,6-hexayl hexakis(dihydrogen phosphate), dipotassium salt

Feng, Xionghan;Yan, Yupeng;Wan, Biao;Li, Wei;Jaisi, Deb P.;Zheng, Lirong;Zhang, Jing;Liu, Fan published 《Enhanced Dissolution and Transformation of ZnO Nanoparticles: The Role of Inositol Hexakisphosphate》. The research results were published in《Environmental Science & Technology》 in 2016.Name: rel-(1R,2r,3S,4R,5s,6S)-Cyclohexane-1,2,3,4,5,6-hexayl hexakis(dihydrogen phosphate), dipotassium salt The article conveys some information:

The toxicity, reactivity, and behavior of ZnO nanoparticles (NPs) released in the environment highly depend on environmental conditions. Myo-inositol hexakisphosphate (IHP), a common organic phosphate, may interact with NPs and generate new transformation products. Here, the role of IHP in mediating the dissolution and transformation of ZnO NPs was studied in the laboratory kinetic experiments using powder x-ray diffraction, attenuated total reflectance FTIR spectroscopy, 31P NMR spectroscopy, high-resolution transmission electronic microscopy, and synchrotron-based extended x-ray absorption fine structure spectroscopy. The results indicate that IHP shows a dissolution-precipitation effect, which is different from citrate and EDTA that only enhances Zn dissolution The enhanced dissolution and transformation of ZnO NPs by IHP (<0.5 h) is strikingly faster than that induced by inorganic phosphate (Pi, >3.0 h) at pH 7.0, and the reaction rate increases with decreasing pH and increasing IHP concentration Multitechnique analyses reveal that interaction of ZnO NPs with IHP induces rapid transformation of ZnO NPs into Zn phytate complexes initially and poorly crystalline Zn phytate-like (Zn-IHP) phase finally. ZnO NPs preferentially react with IHP and transform to Zn-IHP when Pi and IHP concurrently coexist in a system. Overall, results from this study contribute to an improved understanding of the role of organic phosphates (e.g., IHP) in the speciation and structural transformation of ZnO NPs, which can be leveraged for remediation of ZnO-polluted water and soils. The experimental procedure involved many compounds, such as rel-(1R,2r,3S,4R,5s,6S)-Cyclohexane-1,2,3,4,5,6-hexayl hexakis(dihydrogen phosphate), dipotassium salt (cas: 129832-03-7) .

rel-(1R,2r,3S,4R,5s,6S)-Cyclohexane-1,2,3,4,5,6-hexayl hexakis(dihydrogen phosphate), dipotassium salt (cas:129832-03-7) is also known as Inositol hexakisphosphate. Phytic acid dipotassium salt is a potent chelator of divalent and trivalent cations, and a major determinant of zinc bioavailability.Name: rel-(1R,2r,3S,4R,5s,6S)-Cyclohexane-1,2,3,4,5,6-hexayl hexakis(dihydrogen phosphate), dipotassium salt

Reference:
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Leon-Aparicio, Daniel et al. published new experimental results with the assistance of cas: 112-62-9

Methyl oleate(cas: 112-62-9) is a fatty acid methyl ester resulting from the formal condensation of the carboxy group of oleic acid with methanol.Synthetic Route of C19H36O2 It is also used in biochemical research as a chromatographic reference standard.

Leon-Aparicio, Daniel;Sanchez-Solano, Alfredo;Arreola, Jorge;Perez-Cornejo, Patricia published 《Oleic acid blocks the calcium-activated chloride channel TMEM16A/ANO1》. The research results were published in《Biochimica et Biophysica Acta, Molecular and Cell Biology of Lipids》 in 2022.Synthetic Route of C19H36O2 The article conveys some information:

The calcium-activated chloride channel TMEM16A (ANO1) supports the passive movement of chloride ions across membranes and controls critical cell functions. Here we study the block of wild-type and mutant TMEM16A channels expressed in HEK293 cells by oleic acid, a monounsaturated omega-9 fatty acid beneficial for cardiovascular health. We found that oleic acid irreversibly blocks TMEM16A in a dose- and voltage-dependent manner at low intracellular Ca2+. We tested whether oleic acid interacted with the TMEM16A pore, varying the permeant anion concentration and mutating pore residues. Lowering the permeating anion concentration in the intracellular side did nothing but the blockade was intensified by increasing the anion concentration in the extracellular side. However, the blockade of the pore mutants E633A and I641A was voltage-independent, and the I641A IC50, a mutant with the inner hydrophobic gate in disarray, increased 16-fold. Furthermore, the uncharged methyl-oleate blocked 20-24% of the wild-type and I641A channels regardless of voltage. Our findings suggest that oleic acid inhibits TMEM16A by an allosteric mechanism after the elec. field drives oleic acid’s charged moiety inside the pore. Block of TMEM16A might be why oleic acid has a beneficial impact on the cardiovascular system. The experimental procedure involved many compounds, such as Methyl oleate (cas: 112-62-9) .

Methyl oleate(cas: 112-62-9) is a fatty acid methyl ester resulting from the formal condensation of the carboxy group of oleic acid with methanol.Synthetic Route of C19H36O2 It is also used in biochemical research as a chromatographic reference standard.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Hayashi, Hiroyuki et al. published new progress in experiments with the help of cas: 93-92-5

1-Phenylethyl acetate(cas:93-92-5) is a carboxylic ester. Reference of 1-Phenylethyl acetate It may be prepared by acetylation of methyl phenyl carbinol; from benzaldehyde by reacting with magnesium methyl bromide and subsequent acetylation; from 1-bromoethylbenzene and silver acetate in acetic acid.

Reference of 1-Phenylethyl acetate《Insight into the Mechanism of the Acylation of Alcohols with Acid Anhydrides Catalyzed by Phosphoric Acid Derivatives》 was published in 2021. The authors were Hayashi, Hiroyuki;Yasukochi, Shotaro;Sakamoto, Tatsuhiro;Hatano, Manabu;Ishihara, Kazuaki, and the article was included in《Journal of Organic Chemistry》. The author mentioned the following in the article:

Insight into the mechanism of a safe, simple, and inexpensive phosphoric acid (H3PO4)-catalyzed acylation of alcs. with acid anhydrides is described. The corresponding in situ-generated diacylated mixed anhydrides, unlike traditionally proposed monoacylated mixed anhydrides, are proposed as the active species. In particular, the diacylated mixed anhydrides act as efficient catalytic acyl transfer reagents rather than as Bronsted acid catalysts simply activating acid anhydrides. Remarkably, highly efficient phosphoric acid (1-3 mol %)-catalyzed acylation of alcs. with acid anhydrides was achieved and a 23 g scale synthesis of an ester was demonstrated. Also, phosphoric acid catalyst was effective for synthetically useful esterification from carboxylic acids, alcs., and acid anhydride. Moreover, with regard to recent developments in chiral 1,1′-bi-2-naphthol (BINOL)-derived phosphoric acid diester catalysts toward asym. kinetic resolution of alcs. by acylation, some phosphate diesters were examined As a result, a 31P NMR study and a kinetics study strongly supported not only the acid-base cooperative mechanism as previously proposed by other researchers but also the mixed anhydride mechanism as presently proposed by us. To complete the study, the researchers used 1-Phenylethyl acetate (cas: 93-92-5) .

1-Phenylethyl acetate(cas:93-92-5) is a carboxylic ester. Reference of 1-Phenylethyl acetate It may be prepared by acetylation of methyl phenyl carbinol; from benzaldehyde by reacting with magnesium methyl bromide and subsequent acetylation; from 1-bromoethylbenzene and silver acetate in acetic acid.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Cas: 124-06-1 | Han, Yingying et al. made new progress in 2021

Ethyl tetradecanoate(cas: 124-06-1) is a labeled component from essential oil of natural hawthorn perfume. Also frequently used in cosmetics, soaps, and flavorings.Quality Control of Ethyl tetradecanoateEthyl myristate is a long-chain fatty acid ethyl ester resulting from the formal condensation of the carboxy group of myristic acid with the hydroxy group of ethanol.

Han, Yingying;Du, Jinhua;Song, Zhaolin published 《Effects of the yeast endogenous β-glucosidase on hawthorn (Crataegus pinnatifida Bunge) wine ethyl carbamate and volatile compounds》 in 2021. The article was appeared in 《Journal of Food Composition and Analysis》. They have made some progress in their research.Quality Control of Ethyl tetradecanoate The article mentions the following:

In this study, twenty-three com. yeasts were inoculated into hawthorn (Crataegus pinnatifida, Bunge (Rosaceae)) extracted juice to explore their fermentation characteristics, beta-glucosidase activity, Et carbamate production, volatile compounds of resulted wines, along with the relationship of beta-glucosidase activity on Et carbamate and volatile compounds beta-Glucosidases were yeast and culture medium dependence. However, their activities in wines were merely 9.50%-30.7% of that in YM (yeast extract, malt extract) medium. Et carbamate, which was also yeast dependence, was correlated with beta-glucosidase (0.426*) whereas less affected by physicochem. indexes of hawthron wines. Volatile compounds were not correlated with beta-glucosidase activity whereas related to the physicochem. indexes. alpha-Terpineol, which was originally existed in the juice, was increased by the fermentation, while (-) linalool oxide, rose oxide, linalool, terpinen-4-ol, citronellol and nerolidol were newly produced during fermentation FC9 was the most optimal yeast for hawthorn wine making because of its excellent ethanol production, higher beta-glucosidase activity, moderate amounts of volatile compounds, best sensory score and lower EC (5.48μg/L). And Ethyl tetradecanoate (cas: 124-06-1) was used in the research process.

Ethyl tetradecanoate(cas: 124-06-1) is a labeled component from essential oil of natural hawthorn perfume. Also frequently used in cosmetics, soaps, and flavorings.Quality Control of Ethyl tetradecanoateEthyl myristate is a long-chain fatty acid ethyl ester resulting from the formal condensation of the carboxy group of myristic acid with the hydroxy group of ethanol.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Kalra, Rishu et al. published new experimental results with the assistance of cas: 4707-47-5

Methyl 2,4-dihydroxy-3,6-dimethylbenzoate(4707-47-5) is used in biological study as role of androgens in inducing distinct response of epithelial-mesenchymal transition factors in human prostate cancer cells.HPLC of Formula: 4707-47-5

HPLC of Formula: 4707-47-5In 2021, Kalra, Rishu;Conlan, Xavier A.;Areche, Carlos;Dilawari, Rahul;Goel, Mayurika published 《Metabolite profiling of the indian food spice lichen, Pseudevernia furfuracea combined with optimisedextraction methodology to obtain bioactive phenolic compounds》. 《Frontiers in Pharmacology》published the findings. The article contains the following contents:

Pseudevernia furfuracea (L.) Zopf (Parmeliaceae) is a well-known epiphytic lichen commonly used in Indian spice mixtures and food preparations such as curries. This study is an attempt to find the best extraction methodol. with respect to extractive yield, total polyphenolic content (TPC), total flavonoid content and antioxidant activities of lichen P. furfuracea. Two phenolic compounds, atraric acid and olivetoric acid were isolated and quantified in their resp. extracts with the aid of reverse phase high performance liquid chromatog. (RP-HPLC). The highest concentration of both the compounds, atraric acid (4.89 mg/g DW) and olivetoric acid (11.46 mg/g DW) were found in 70% methanol extract A direct correlation was also observed between the concentrations of these compounds with the free radical scavenging potential of the extracts which might contribute towards the antioxidant potential of the extract Moreover, SEM and HPLC anal. which was used to study the effect of pre-processing on extraction process highlighted the capacity of a mixer grinder technique for improved separation of surface localized metabolites and enrichment of the fraction. An investigation of the chem. profile of the bioactive extract 70% methanol extract using UHPLC-DAD-MS lead to tentative identification of forty nine compounds This extract was also assessed towards HEK 293 T cell line for cytotoxicity anal. Concentration range of 0.156 to 100 μg/mL of PF70M extract exhibited no significant cell death as compared to control. Further, the active extract showed protective effect against hydroxyl radical′s destructive effects on DNA when assessed using DNA nicking assay. Based upon this, it can be concluded that optimization of extraction solvent, sample pre-processing and extraction techniques can be useful in extraction of specific antioxidant metabolites. The experimental procedure involved many compounds, such as Methyl 2,4-dihydroxy-3,6-dimethylbenzoate (cas: 4707-47-5) .

Methyl 2,4-dihydroxy-3,6-dimethylbenzoate(4707-47-5) is used in biological study as role of androgens in inducing distinct response of epithelial-mesenchymal transition factors in human prostate cancer cells.HPLC of Formula: 4707-47-5

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Cas: 93-92-5 | Feng, Chengliangpublished an article in 2018

1-Phenylethyl acetate(cas:93-92-5) is a carboxylic ester. Product Details of 93-92-5 It may be prepared by acetylation of methyl phenyl carbinol; from benzaldehyde by reacting with magnesium methyl bromide and subsequent acetylation; from 1-bromoethylbenzene and silver acetate in acetic acid.

Feng, Chengliang;Yan, Bin;Yin, Guibo;Chen, Junqing;Ji, Min published 《Fe(ClO4)3·H2O-Catalyzed Ritter Reaction: A Convenient Synthesis of Amides from Esters and Nitriles》. The research results were published in《Synlett》 in 2018.Product Details of 93-92-5 The article conveys some information:

An efficient and inexpensive method was developed for the synthesis of N-substituted amides RC(O)NHR1 [R = Me, cyclopropyl, Ph, etc.; R1 = t-Bu, c-hexyl, Bn, etc.] via Fe(ClO4)3·H2O-catalyzed Ritter reaction of nitriles with esters. Fe(ClO4)3·H2O was an economically efficient catalyst for Ritter reaction under solvent-free conditions and provided the corresponding amides in high to excellent yields. And 1-Phenylethyl acetate (cas: 93-92-5) was used in the research process.

1-Phenylethyl acetate(cas:93-92-5) is a carboxylic ester. Product Details of 93-92-5 It may be prepared by acetylation of methyl phenyl carbinol; from benzaldehyde by reacting with magnesium methyl bromide and subsequent acetylation; from 1-bromoethylbenzene and silver acetate in acetic acid.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Explore more uses of cas: 4707-47-5 | Biochemical Systematics and Ecology

Methyl 2,4-dihydroxy-3,6-dimethylbenzoate(4707-47-5) is used in biological study as role of androgens in inducing distinct response of epithelial-mesenchymal transition factors in human prostate cancer cells.Name: Methyl 2,4-dihydroxy-3,6-dimethylbenzoate

Youn, Ui Joung;So, Jae Eun;Kim, Ji Hee;Han, Se Jong;Park, Hyun;Kim, Il Chan;Yim, Jung Han published 《Chemical constituents from the Antarctic lichen, Stereocaulon caespitosum》 in 2018. The article was appeared in 《Biochemical Systematics and Ecology》. They have made some progress in their research.Name: Methyl 2,4-dihydroxy-3,6-dimethylbenzoate The article mentions the following:

A phytochem. study of the methanol extract of the Antarctic lichen Stereocaulon caespitosum Redgr. led to the isolation of a tridepside (1), two depsides (2 and 3), a montagnetol derivative (4), and four mono-phenolic compounds (5-8). The structures of these compounds were confirmed by 1D- and 2D-NMR (NMR) experiments, as well as by comparison with published values. This is the first phytochem. study of S. caespitosum. In particular, compounds 1, 3, 4, and 8 have been isolated for the first time from the genus Stereocaulon and the family Stereocaulaceae. The chemotaxonomic significance of the isolated compounds is discussed. To complete the study, the researchers used Methyl 2,4-dihydroxy-3,6-dimethylbenzoate (cas: 4707-47-5) .

Methyl 2,4-dihydroxy-3,6-dimethylbenzoate(4707-47-5) is used in biological study as role of androgens in inducing distinct response of epithelial-mesenchymal transition factors in human prostate cancer cells.Name: Methyl 2,4-dihydroxy-3,6-dimethylbenzoate

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

New progress of cas: 93-92-5 | Biotechnology Journal 2019

1-Phenylethyl acetate(cas:93-92-5) is a carboxylic ester. Reference of 1-Phenylethyl acetate It may be prepared by acetylation of methyl phenyl carbinol; from benzaldehyde by reacting with magnesium methyl bromide and subsequent acetylation; from 1-bromoethylbenzene and silver acetate in acetic acid.

Meyer, Lars-Erik;Gummesson, Anja;Kragl, Udo;von Langermann, Jan published 《Development of Ionic Liquid-Water-Based Thermomorphic Solvent (TMS)-Systems for Biocatalytic Reactions》. The research results were published in《Biotechnology Journal》 in 2019.Reference of 1-Phenylethyl acetate The article conveys some information:

The applicability of ionic liquid-water-based thermomorphic solvent (TMS)-systems with an upper critical solution temperature for homogeneous biocatalysis is investigated. Cholinium- and imidazolium-based ionic liquids are used to facilitate a temperature-dependent phase change, which can be easily fine-tuned by adding salts or polar organic solvents. Within the TMS-system, a high enzymic activity and subsequent full conversion is achieved in the intermittent monophasic reaction system of the TMS-system. Therefore, the biocatalyst can be easily recycled after separating the phases at lower temperatures The experimental procedure involved many compounds, such as 1-Phenylethyl acetate (cas: 93-92-5) .

1-Phenylethyl acetate(cas:93-92-5) is a carboxylic ester. Reference of 1-Phenylethyl acetate It may be prepared by acetylation of methyl phenyl carbinol; from benzaldehyde by reacting with magnesium methyl bromide and subsequent acetylation; from 1-bromoethylbenzene and silver acetate in acetic acid.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics