Tag: M.W=350-400

Yin, Lu published the artcileInduction and modulation of supramolecular chirality in side-chain azobenzene polymers through the covalent chiral domino effect, Product Details of C23H28N2O4, the publication is Science China: Chemistry (2021), 64(12), 2105-2110, database is CAplus.

Induction, transfer, and modulation of intriguing supramol. chirality were achieved in a chiral domino-type polymer system using a chiral α-end azobenzene (Azo) moiety as one chiral terminus and achiral Azo repeating units as building blocks. The Azo polymers prepared by atom transfer radical polymerization were imparted with well-controlled chain lengths and a chiral moiety at a well-defined position. One chiral terminus can effectively dictate the helical orientation of the achiral Azo stacks in the aggregation state. The spacer length between the chiral residue and the achiral repeating units dominates the preferred handedness of the side-chain Azo stacks. For instance, the R-configuration moiety with a short alkyl chain (with 0, 2, and 3 carbons) induces right-handed supramol. chirality, whereas those with long alkyl chains (with 4, 5, and 6 carbons) induce the opposite helical orientation of the Azo units. Moreover, the chiral regulation of polymer aggregates is successfully achieved using the unique photoisomerization transition of the Azo chromophore and the heat-assisted reassembly approach. Chiral induction and chiral-to-achiral communication are further verified via theor. simulations.

Science China: Chemistry published new progress about 135529-02-1. 135529-02-1 belongs to esters-buliding-blocks, auxiliary class azo,Alkenyl,Benzene,Ester,Ether, name is 6-(4-((4-Methoxyphenyl)diazenyl)phenoxy)hexyl methacrylate, and the molecular formula is C18H17NO8, Product Details of C23H28N2O4.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Yin, Lu published the artcileSupramolecular chirality induced by chiral solvation in achiral cyclic Azo-containing polymers: topological effects on chiral aggregation, HPLC of Formula: 135529-02-1, the publication is Polymer Chemistry (2018), 9(6), 769-776, database is CAplus.

Herein, a series of azobenzene (Azo)-containing side-chain cyclic polymers were successfully synthesized by combining atom transfer radical polymerization (ATRP) and Cu(I)-catalyzed azide/alkyne cycloaddition (CuAAc) “click” reaction. The aggregates of linear and cyclic Azo polymers in a dichloroethane/limonene mixed solvent were characterized by CD (CD) and UV-visible spectroscopy, demonstrating that the topol. structural constraint and mol. mass of cyclic polymers have clear effects on the supramol. chirality driven by a chiral solvent. The difference between linear and cyclic Azo aggregates in supramol. chirality became less distinct with increasing mol. mass of Azo polymers. The chiroptical switch of cyclic Azo polymers was firstly constructed by trans-cis photoisomerization and cis-trans heating-assisted reorganization processes. These interesting findings suggest that the cyclic topol. has a clear influence on the behavior of supramol. chirality induced by chiral limonene.

Polymer Chemistry published new progress about 135529-02-1. 135529-02-1 belongs to esters-buliding-blocks, auxiliary class azo,Alkenyl,Benzene,Ester,Ether, name is 6-(4-((4-Methoxyphenyl)diazenyl)phenoxy)hexyl methacrylate, and the molecular formula is C8H7ClO3, HPLC of Formula: 135529-02-1.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Yin, Lu published the artcileInduction and modulation of supramolecular chirality in side-chain azobenzene polymers through the covalent chiral domino effect, Product Details of C23H28N2O4, the publication is Science China: Chemistry (2021), 64(12), 2105-2110, database is CAplus.

Induction, transfer, and modulation of intriguing supramol. chirality were achieved in a chiral domino-type polymer system using a chiral α-end azobenzene (Azo) moiety as one chiral terminus and achiral Azo repeating units as building blocks. The Azo polymers prepared by atom transfer radical polymerization were imparted with well-controlled chain lengths and a chiral moiety at a well-defined position. One chiral terminus can effectively dictate the helical orientation of the achiral Azo stacks in the aggregation state. The spacer length between the chiral residue and the achiral repeating units dominates the preferred handedness of the side-chain Azo stacks. For instance, the R-configuration moiety with a short alkyl chain (with 0, 2, and 3 carbons) induces right-handed supramol. chirality, whereas those with long alkyl chains (with 4, 5, and 6 carbons) induce the opposite helical orientation of the Azo units. Moreover, the chiral regulation of polymer aggregates is successfully achieved using the unique photoisomerization transition of the Azo chromophore and the heat-assisted reassembly approach. Chiral induction and chiral-to-achiral communication are further verified via theor. simulations.

Science China: Chemistry published new progress about 135529-02-1. 135529-02-1 belongs to esters-buliding-blocks, auxiliary class azo,Alkenyl,Benzene,Ester,Ether, name is 6-(4-((4-Methoxyphenyl)diazenyl)phenoxy)hexyl methacrylate, and the molecular formula is C18H17NO8, Product Details of C23H28N2O4.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Yin, Lu published the artcileSupramolecular chirality induced by chiral solvation in achiral cyclic Azo-containing polymers: topological effects on chiral aggregation, HPLC of Formula: 135529-02-1, the publication is Polymer Chemistry (2018), 9(6), 769-776, database is CAplus.

Herein, a series of azobenzene (Azo)-containing side-chain cyclic polymers were successfully synthesized by combining atom transfer radical polymerization (ATRP) and Cu(I)-catalyzed azide/alkyne cycloaddition (CuAAc) “click” reaction. The aggregates of linear and cyclic Azo polymers in a dichloroethane/limonene mixed solvent were characterized by CD (CD) and UV-visible spectroscopy, demonstrating that the topol. structural constraint and mol. mass of cyclic polymers have clear effects on the supramol. chirality driven by a chiral solvent. The difference between linear and cyclic Azo aggregates in supramol. chirality became less distinct with increasing mol. mass of Azo polymers. The chiroptical switch of cyclic Azo polymers was firstly constructed by trans-cis photoisomerization and cis-trans heating-assisted reorganization processes. These interesting findings suggest that the cyclic topol. has a clear influence on the behavior of supramol. chirality induced by chiral limonene.

Polymer Chemistry published new progress about 135529-02-1. 135529-02-1 belongs to esters-buliding-blocks, auxiliary class azo,Alkenyl,Benzene,Ester,Ether, name is 6-(4-((4-Methoxyphenyl)diazenyl)phenoxy)hexyl methacrylate, and the molecular formula is C8H7ClO3, HPLC of Formula: 135529-02-1.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Yin, Lu published the artcileInduction and modulation of supramolecular chirality in side-chain azobenzene polymers through the covalent chiral domino effect, Product Details of C23H28N2O4, the publication is Science China: Chemistry (2021), 64(12), 2105-2110, database is CAplus.

Induction, transfer, and modulation of intriguing supramol. chirality were achieved in a chiral domino-type polymer system using a chiral α-end azobenzene (Azo) moiety as one chiral terminus and achiral Azo repeating units as building blocks. The Azo polymers prepared by atom transfer radical polymerization were imparted with well-controlled chain lengths and a chiral moiety at a well-defined position. One chiral terminus can effectively dictate the helical orientation of the achiral Azo stacks in the aggregation state. The spacer length between the chiral residue and the achiral repeating units dominates the preferred handedness of the side-chain Azo stacks. For instance, the R-configuration moiety with a short alkyl chain (with 0, 2, and 3 carbons) induces right-handed supramol. chirality, whereas those with long alkyl chains (with 4, 5, and 6 carbons) induce the opposite helical orientation of the Azo units. Moreover, the chiral regulation of polymer aggregates is successfully achieved using the unique photoisomerization transition of the Azo chromophore and the heat-assisted reassembly approach. Chiral induction and chiral-to-achiral communication are further verified via theor. simulations.

Science China: Chemistry published new progress about 135529-02-1. 135529-02-1 belongs to esters-buliding-blocks, auxiliary class azo,Alkenyl,Benzene,Ester,Ether, name is 6-(4-((4-Methoxyphenyl)diazenyl)phenoxy)hexyl methacrylate, and the molecular formula is C18H17NO8, Product Details of C23H28N2O4.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Yin, Lu published the artcileSupramolecular chirality induced by chiral solvation in achiral cyclic Azo-containing polymers: topological effects on chiral aggregation, HPLC of Formula: 135529-02-1, the publication is Polymer Chemistry (2018), 9(6), 769-776, database is CAplus.

Herein, a series of azobenzene (Azo)-containing side-chain cyclic polymers were successfully synthesized by combining atom transfer radical polymerization (ATRP) and Cu(I)-catalyzed azide/alkyne cycloaddition (CuAAc) “click” reaction. The aggregates of linear and cyclic Azo polymers in a dichloroethane/limonene mixed solvent were characterized by CD (CD) and UV-visible spectroscopy, demonstrating that the topol. structural constraint and mol. mass of cyclic polymers have clear effects on the supramol. chirality driven by a chiral solvent. The difference between linear and cyclic Azo aggregates in supramol. chirality became less distinct with increasing mol. mass of Azo polymers. The chiroptical switch of cyclic Azo polymers was firstly constructed by trans-cis photoisomerization and cis-trans heating-assisted reorganization processes. These interesting findings suggest that the cyclic topol. has a clear influence on the behavior of supramol. chirality induced by chiral limonene.

Polymer Chemistry published new progress about 135529-02-1. 135529-02-1 belongs to esters-buliding-blocks, auxiliary class azo,Alkenyl,Benzene,Ester,Ether, name is 6-(4-((4-Methoxyphenyl)diazenyl)phenoxy)hexyl methacrylate, and the molecular formula is C8H7ClO3, HPLC of Formula: 135529-02-1.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Markellos, Christos published the artcileOlive oil intake and cancer risk: A systematic review and meta-analysis, Recommanded Product: Methyl docosanoate, the main research area is .

Background: Research evidence has established the beneficial effects of diet in cancer prevention; various epidemiol. studies have suggested that olive oil component could play a role in decreasing cancer risk. This systematic review and meta-anal. aims to investigate the association between olive oil consumption, cancer risk and prognosis. Methods: A systematic search was conducted in PubMed, EMBASE and Google Scholar databases (end-of-search: May 10, 2020). Pooled relative risk (RR) and 95% confidence intervals (95% CIs) were estimated with random-effects (DerSimonian-Laird) models. Subgroup analyses, sensitivity analyses and meta-regression anal. were also performed. Results: 45 studies were included in the meta-anal.; 37 were case-control (17,369 cases and 28,294 controls) and 8 were cohort studies (12,461 incident cases in a total cohort of 929,771 subjects). Highest olive oil consumption was associated with 31% lower likelihood of any cancer (pooled RR = 0.69, 95%CI: 0.62-0.77), breast (RR = 0.67, 95%CI: 0.52-0.86), gastrointestinal (RR = 0.77, 95%CI: 0.66-0.89), upper aerodigestive (RR = 0.74, 95%CI: 0.60-0.91) and urinary tract cancer (RR = 0.46, 95%CI: 0.29-0.72). Significant overall effects spanned both Mediterranean and non-Mediterranean participants, studies presenting a multivariate and a univariate anal. and all subgroups by study quality. Conclusions: Olive oil consumption seems to exert beneficial actions in terms of cancer prevention. Addnl. prospective cohort studies on various cancer types and survivors, as well as large randomized trials, seem desirable.

PLoS One published new progress in CAplus and MEDLINE about 929-77-1, 929-77-1 belongs to class esters-buliding-blocks, name is Methyl docosanoate, and the molecular formula is C23H46O2, Recommanded Product: Methyl docosanoate.

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

Li, Pei-Xia published the artcileChemical constituents analysis of ethyl acetate extract from MSR-1707 by GC-MS, SDS of cas: 929-77-1, the main research area is chem constituent analysis ethyl acetate extract MSR.

To analyze the chem. constituents of Et acetate extract from MSR-1707 to promote the rational utilization of the mushroom resources. MSR-1707 belongs to the genus Nigrospora sp. It was extracted by Et acetate, then the extract was analyzed by Gas Chromatog.-Mass Spectrometer (GC-MS). Identification of compounds was achieved according to their GC retention indexes (RI) and database search using the library of NIST05, as well as a comparison of the fragmentation pattern of the mass spectra with data published in the literature. Seventy-three compounds were separated by gas chromatog. Based on the NIST05 spectral library and corresponding literature information, fifty-three compounds were identified. Their relative percentage of contents accounted for 95.62% of the outflow peak. Some of the identified peaks are 9-Octadecenoic acid, Me ester(E)(18.50%),9-Tricosene(Z)(8.30%), 13-Docosenamide (E)(5.26%) and Myristic acid glycidyl ester (3.11%). This is the first report of chem. constituents of the Et acetate extract of Nigrospora sp. using GC-MS, which offer some theor. basis for the further exploration and application of this mushroom.

Asian Journal of Biology published new progress about Analysis. 929-77-1 belongs to class esters-buliding-blocks, name is Methyl docosanoate, and the molecular formula is C23H46O2, SDS of cas: 929-77-1.

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

Belal, Babita published the artcileAltitudinal variations in chemical profile and antioxidant activities of lentil (Lens culinaris Medik.) genotypes, Synthetic Route of 929-77-1, the main research area is Lens phytoconstituent antioxidant activity genotype.

The present investigation was carried out to evaluate the altitudinal variation between two lentil (Lens culinaris Medik.) genotypes on the basis of their chem. profile, total phenolic content and antioxidant activitiy. Pulse samples were collected from two different altitudes of Uttarakhand state. The chem. profiling was done via Gas chromatog.-Mass spectrometry anal. A total of 45 and 33 phytoconstituents accounting for 76.51% and 81.03% of the total extract has been identified in the sample from lower altitude and higher altitude resp. Antioxidant activity was determined in terms of 2, 2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging, hydroxyl radical scavenging and metal chelating assays. Results revealed that the genotype from higher altitude exhibits higher antioxidant potential than the genotype from lower altitude. A significant pos. correlation has been observed between altitude and total phenolic content, whereas a significant neg. correlation between altitude and 50% inhibitory concentration (IC50) of both genotypes.

Pharma Innovation published new progress about Genotypes. 929-77-1 belongs to class esters-buliding-blocks, name is Methyl docosanoate, and the molecular formula is C23H46O2, Synthetic Route of 929-77-1.

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

Ochieng, Brian O. published the artcileDynamics in nutrients, sterols and total flavonoid content during processing of the edible Long-Horned grasshopper (Ruspolia differens Serville) for food, Recommanded Product: Methyl docosanoate, the main research area is Ruspolia flavonoid campesterol beta sitosterol dynamic nutrient; Food and nutritional security; Nutrients; Post-harvest processing; Ruspolia differens; Sterols; Tettigoniidae; Total flavonoid.

Long-horned grasshopper (Ruspolia differens Serville) is a tasty delicacy in over 20 African countries. This study evaluated the impact of diverse post-harvest thermal treatment (blanching, boiling, toasting, and deep-frying) on the nutrients, total flavonoid content and sterols preservation of R. differens products. Crude protein, ash, and fiber of R. differens was drastically reduced by deep-frying technique. There was increase in Omega-3 (α-linolenic acid), Omega-6 fatty acid (linoleic and arachidonic acids) and sterols [(22Z)-27-Norergosta-5,22-dien-3β-ol, cholesterol, campesterol, cholest-4-ene-3-one and β-sitosterol] and flavonoids (2-3 folds) during blanching compared to other techniques. The iron and zinc content increased significantly in blanched and boiled products of R. differens. Thus, losses of nutrients, total flavonoid content and sterols during processing of R. differens for food can be mitigated by employing blanching technique, which is cheaper and least time-consuming. The implications of these dietary and therapeutic compounds on human nutrition and health are discussed.

Food Chemistry published new progress about Blanching. 929-77-1 belongs to class esters-buliding-blocks, name is Methyl docosanoate, and the molecular formula is C23H46O2, Recommanded Product: Methyl docosanoate.

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