Bielicka-Daszkiewicz, Katarzyna’s team published research in Microchemical Journal in 169 | CAS: 10287-53-3

Microchemical Journal published new progress about 10287-53-3. 10287-53-3 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Ester, name is Ethyl 4-dimethylaminobenzoate, and the molecular formula is C11H15NO2, Quality Control of 10287-53-3.

Bielicka-Daszkiewicz, Katarzyna published the artcileExtraction of organic compounds released from dental materials, Quality Control of 10287-53-3, the publication is Microchemical Journal (2021), 106594, database is CAplus.

Extraction method based on polymer inclusion membranes device was used for isolation organic compounds released from dental materials. These compounds were isolated form artificial saliva solution Three different membranes were used, it based on cellulose triacetate and 2-nitrophenyloctyl ether as plasticizer. One of membranes addnl. contained Aliquat-336 as carrier of analytes. The best efficiency of polymer membranes was achieved between 80 and 100% for three components membrane. The retention properties of polymeric membranes was described and confirmed using Hansen Solubility Parameter determined for each isolated compound and membrane components. Determination of this parameter allows to describe the interaction between isolated compound and membrane, and conclude which membrane composition gives the best retention properties.

Microchemical Journal published new progress about 10287-53-3. 10287-53-3 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Ester, name is Ethyl 4-dimethylaminobenzoate, and the molecular formula is C11H15NO2, Quality Control of 10287-53-3.

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

Zinger, Nicole’s team published research in Neurology(R) neuroimmunology & neuroinflammation in 9 | CAS: 624-49-7

Neurology(R) neuroimmunology & neuroinflammation published new progress about 624-49-7. 624-49-7 belongs to esters-buliding-blocks, auxiliary class Inhibitor,Natural product, name is Dimethyl fumarate, and the molecular formula is C4H4Br2N2, Name: Dimethyl fumarate.

Zinger, Nicole published the artcileDimethyl Fumarate Reduces Inflammation in Chronic Active Multiple Sclerosis Lesions., Name: Dimethyl fumarate, the publication is Neurology(R) neuroimmunology & neuroinflammation (2022), 9(2), database is MEDLINE.

BACKGROUND AND OBJECTIVES: To determine the effects of dimethyl fumarate (DMF) and glatiramer acetate on iron content in chronic active lesions in patients with multiple sclerosis (MS) and in human microglia in vitro. METHODS: This was a retrospective observational study of 34 patients with relapsing-remitting MS and clinically isolated syndrome treated with DMF or glatiramer acetate. Patients had lesions with hyperintense rims on quantitative susceptibility mapping, were treated with DMF or glatiramer acetate (GA), and had a minimum of 2 on-treatment scans. Changes in susceptibility in rim lesions were compared among treatment groups in a linear mixed effects model. In a separate in vitro study, induced pluripotent stem cell-derived human microglia were treated with DMF or GA, and treatment-induced changes in iron content and activation state of microglia were compared. RESULTS: Rim lesions in patients treated with DMF had on average a 2.77-unit reduction in susceptibility per year over rim lesions in patients treated with GA (bootstrapped 95% CI -5.87 to -0.01), holding all other variables constant. Moreover, DMF but not GA reduced inflammatory activation and concomitantly iron content in human microglia in vitro. DISCUSSION: Together, our data indicate that DMF-induced reduction of susceptibility in MS lesions is associated with a decreased activation state in microglial cells. We have demonstrated that a specific disease modifying therapy, DMF, decreases glial activity in chronic active lesions. Susceptibility changes in rim lesions provide an in vivo biomarker for the effect of DMF on microglial activity. CLASSIFICATION OF EVIDENCE: This study provided Class III evidence that DMF is superior to GA in the presence of iron as a marker of inflammation as measured by MRI quantitative susceptibility mapping.

Neurology(R) neuroimmunology & neuroinflammation published new progress about 624-49-7. 624-49-7 belongs to esters-buliding-blocks, auxiliary class Inhibitor,Natural product, name is Dimethyl fumarate, and the molecular formula is C4H4Br2N2, Name: Dimethyl fumarate.

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

Sokolov, Alexey S.’s team published research in Helvetica Chimica Acta in 105 | CAS: 624-49-7

Helvetica Chimica Acta published new progress about 624-49-7. 624-49-7 belongs to esters-buliding-blocks, auxiliary class Inhibitor,Natural product, name is Dimethyl fumarate, and the molecular formula is C22H12F6O6S2, Synthetic Route of 624-49-7.

Sokolov, Alexey S. published the artcileGeneration of Cyclopentadiene for Diels-Alder Reactions by Visible-Light Irradiation of Iron Sandwich Complexes, Synthetic Route of 624-49-7, the publication is Helvetica Chimica Acta (2022), 105(4), e202100246, database is CAplus.

Cyclopentadienes readily undergo fast and selective Diels-Alder reactions which can be used for conjugation of biomols. and polymers. Herein authors present a new method for the photochem. generation of cyclopentadienes by the visible light irradiation of the iron complexes [(C5H4R)Fe(arene)]+. This reaction proceeds at room temperature, in water, and in the presence of potentially interfering amino acids. Free cyclopentadiene is trapped by dienophiles to give the corresponding Diels-Alder adducts in 72-95% yield.

Helvetica Chimica Acta published new progress about 624-49-7. 624-49-7 belongs to esters-buliding-blocks, auxiliary class Inhibitor,Natural product, name is Dimethyl fumarate, and the molecular formula is C22H12F6O6S2, Synthetic Route of 624-49-7.

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

Netz, Astrid’s team published research in European Journal of Organic Chemistry in | CAS: 924-99-2

European Journal of Organic Chemistry published new progress about 924-99-2. 924-99-2 belongs to esters-buliding-blocks, auxiliary class Alkenyl,Amine,Aliphatic hydrocarbon chain,Ester, name is Ethyl 3-(dimethylamino)acrylate, and the molecular formula is C7H13NO2, Application In Synthesis of 924-99-2.

Netz, Astrid published the artcileFacial diastereoselectivity in cationic propargylations with planar-chiral areneCr(CO)3-substituted propargyl cations, Application In Synthesis of 924-99-2, the publication is European Journal of Organic Chemistry (2005), 1823-1833, database is CAplus.

The planar-chiral (o-methoxyphenyl)chromium tricarbonyl-substituted propargyl cation reacts with silyl enol ether derivatives with poor and with enamines with good facial diastereoselectivity to give rise to the (arene)carbonylchromium-substituted propargylated cyclohexan-2-ones, and carboxylic acid, γ-lactone, cyclopentan-2-one, and esters. Structural correlations were unambiguously deduced from x-ray structure. The origin of facial diastereoselectivity with this class of organometallic electrophiles lies in steric and stereoelectronic biases rather than in purely electronic nucleophilicity.

European Journal of Organic Chemistry published new progress about 924-99-2. 924-99-2 belongs to esters-buliding-blocks, auxiliary class Alkenyl,Amine,Aliphatic hydrocarbon chain,Ester, name is Ethyl 3-(dimethylamino)acrylate, and the molecular formula is C7H13NO2, Application In Synthesis of 924-99-2.

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

Huang, Sijia’s team published research in Polymer Chemistry in 11 | CAS: 19788-49-9

Polymer Chemistry published new progress about 19788-49-9. 19788-49-9 belongs to esters-buliding-blocks, auxiliary class Thiol,Aliphatic hydrocarbon chain,Ester, name is Ethyl 2-mercaptopropanoate, and the molecular formula is C5H10O2S, Category: esters-buliding-blocks.

Huang, Sijia published the artcileChemical recycling of poly(thiourethane) thermosets enabled by dynamic thiourethane bonds, Category: esters-buliding-blocks, the publication is Polymer Chemistry (2020), 11(43), 6879-6883, database is CAplus.

Recycling of polyurethanes is largely infeasible due to the harsh reprocessing conditions and associated risks of side reactions and degradation whereas polymer networks incorporating dynamic covalent bonds represent an attractive approach to the design of recyclable materials. Here, we report findings on the dynamic nature of thiourethanes, and their application as a new class of recyclable analogs of urethane materials. A series of small mol. experiments was initially conducted to determine the equilibrium constant and exchange reaction kinetic constant for the thiol-isocyanate reaction. Furthermore, incorporating those thiourethane moieties into a cross-linked network resulted in thermoset materials that are readily depolymerized to liquid oligomers. The resultant oligomers can be re-crosslinked to thiourethanes without any loss of performance nor change in mech. properties (peak stress of 25 MPa with max strain of 200%). Moreover, the recycled thiol oligomers from thiourethane network polymers could potentially be transformed into other materials with mech. properties that exceed those of the initial, pristine thiourethane materials. Overall, the ease with which these polythiourethanes are polymerized, recycled and reformulated gives a new direction and hope in the design of sustainable polymers.

Polymer Chemistry published new progress about 19788-49-9. 19788-49-9 belongs to esters-buliding-blocks, auxiliary class Thiol,Aliphatic hydrocarbon chain,Ester, name is Ethyl 2-mercaptopropanoate, and the molecular formula is C5H10O2S, Category: esters-buliding-blocks.

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

Barkane, Anda’s team published research in Polymer in 255 | CAS: 15625-89-5

Polymer published new progress about 15625-89-5. 15625-89-5 belongs to esters-buliding-blocks, auxiliary class Polymerization Reagents,Crosslinkers, name is Trimethylolpropane triacrylate, and the molecular formula is C15H20O6, HPLC of Formula: 15625-89-5.

Barkane, Anda published the artcileSimultaneous wettability and stiffness control of UV-curing vegetable oil resin composites by lignocellulosic components, HPLC of Formula: 15625-89-5, the publication is Polymer (2022), 125154, database is CAplus.

Acrylic resins have various applications, which range from coatings to 3D printing, among others. Following green chem. and environmental preservation trends, the demand for bio-based acrylic resins is growing. Vegetable oil-based resins have arisen to meet the present challenge. However, the performance and tuning of sustainable resin properties still need improvement. Hence, we undertook this study to research tuneable and durable vegetable oil-based UV-curing composite resins. This work reports on vegetable oil-based resin loaded with lignocellulosic components of cellulose nanocrystals (CNC), cellulose nanofibres (CNF), hemicellulose (HC), and lignin (LN). The effects of lignocellulosic components on thermal stability, thermomech. properties, transparency, surface morphol., and wettability were evaluated in detail. In addition, the interaction of lignocellulosic components with the polymer matrix and interface was thoroughly investigated. The intense interaction between lignocellulosic components and the polymer matrix helps to form a strong interface and creates a polymer composite with enhanced thermomech. properties. The composite surface morphol. and wettability can be tuned depending on the lignocellulosic component, i.e., with the addition of HC, CNC, and CNF. Hydrophilic affinity is improved and water wetting angles as low as 8° can be achieved, but with LN a value of 96° was observed, a slight increase in hydrophobicity compared to the vegetable oil (VO) matrix value of 90°. Adding HC and CNC reduced transparency at 500 nm by 14 and 16%, while adding LN and CNF by 18 and 25%, resp. Fourier-transform IR spectroscopy revealed strong interfacial interactions through the hydrogen bonding between CNC, CNF, HC, and the VO polymer. This work will shed light on the lignocellulosic components’ future role in UV-curing resin applications. It also broadens lignocellulosic particles’ application as reinforcing additives for UV-light sensitive polymeric resins.

Polymer published new progress about 15625-89-5. 15625-89-5 belongs to esters-buliding-blocks, auxiliary class Polymerization Reagents,Crosslinkers, name is Trimethylolpropane triacrylate, and the molecular formula is C15H20O6, HPLC of Formula: 15625-89-5.

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

Degotte, Gilles’s team published research in Archiv der Pharmazie (Weinheim, Germany) in 354 | CAS: 121-79-9

Archiv der Pharmazie (Weinheim, Germany) published new progress about 121-79-9. 121-79-9 belongs to esters-buliding-blocks, auxiliary class Natural product, name is Propyl 3,4,5-trihydroxybenzoate, and the molecular formula is C10H12O5, Formula: C10H12O5.

Degotte, Gilles published the artcilePolyhydroxybenzoic acid derivatives as potential new antimalarial agents, Formula: C10H12O5, the publication is Archiv der Pharmazie (Weinheim, Germany) (2021), 354(11), 2100190, database is CAplus and MEDLINE.

With more than 200 million cases and 400,000 related deaths, malaria remains one of the deadliest infectious diseases of 2021. Unfortunately, despite the availability of efficient treatments, we have observed an increase in people infected with malaria since 2015 (from 211 million in 2015 to 229 million in 2019). This trend could partially be due to the development of resistance to all the current drugs. Therefore, there is an urgent need for new alternatives. We have, thus, selected common natural scaffolds, polyhydroxybenzoic acids, and synthesized a library of derivatives to better understand the structure-activity relationships explaining their antiplasmodial effect. Only gallic acid derivatives showed a noticeable potential for further developments. Indeed, they showed a selective inhibitory effect on Plasmodium (IC50 ∼20μM, SI > 5) often associated with interesting water solubility Moreover, this has confirmed the critical importance of free phenolic functions (pyrogallol moiety) for the antimalarial effect. Me 4-benzoxy-3,5-dihydroxybenzoate (39) has, for the first time, been recognized as a potential lead for future research because of its marked inhibitory activity against Plasmodium falciparum and its significant hydrosoly. (3.72 mM).

Archiv der Pharmazie (Weinheim, Germany) published new progress about 121-79-9. 121-79-9 belongs to esters-buliding-blocks, auxiliary class Natural product, name is Propyl 3,4,5-trihydroxybenzoate, and the molecular formula is C10H12O5, Formula: C10H12O5.

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

Garcia Lopez, J.’s team published research in Chemical Communications (Cambridge, United Kingdom) in 55 | CAS: 3052-61-7

Chemical Communications (Cambridge, United Kingdom) published new progress about 3052-61-7. 3052-61-7 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Amide, name is Benzyl diethylcarbamodithioate, and the molecular formula is C12H17NS2, Recommanded Product: Benzyl diethylcarbamodithioate.

Garcia Lopez, J. published the artcileApplication of molecularly imprinted polymer nanoparticles for degradation of the bacterial autoinducer N-hexanoyl homoserine lactone, Recommanded Product: Benzyl diethylcarbamodithioate, the publication is Chemical Communications (Cambridge, United Kingdom) (2019), 55(18), 2664-2667, database is CAplus and MEDLINE.

A novel bacterial quorum quenching system is presented. For the first time the degradation of N-L-hexanoyl homoserine lactone (C6-AHL), a Gram-neg. quorum sensing autoinducer, has been enhanced using molecularly imprinted nanoparticles (MIP NPs) which were prepared using transition state analog of the γ-lactone ring hydrolysis as template.

Chemical Communications (Cambridge, United Kingdom) published new progress about 3052-61-7. 3052-61-7 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Amide, name is Benzyl diethylcarbamodithioate, and the molecular formula is C12H17NS2, Recommanded Product: Benzyl diethylcarbamodithioate.

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

Sun, Ke’s team published research in Macromolecular Chemistry and Physics in 223 | CAS: 15625-89-5

Macromolecular Chemistry and Physics published new progress about 15625-89-5. 15625-89-5 belongs to esters-buliding-blocks, auxiliary class Polymerization Reagents,Crosslinkers, name is Trimethylolpropane triacrylate, and the molecular formula is C17H19N3O7S, Computed Properties of 15625-89-5.

Sun, Ke published the artcileSunlight Induced Polymerization Photoinitiated by Novel Push-Pull Dyes: Indane-1,3-Dione, 1H-Cyclopenta[b]Naphthalene-1,3(2H)-Dione and 4-Dimethoxyphenyl-1-Allylidene Derivatives, Computed Properties of 15625-89-5, the publication is Macromolecular Chemistry and Physics (2022), 223(4), 2100439, database is CAplus.

The free radical polymerization of acrylates photo-initiated by push-pull dye-based photoinitiating systems (PISs) is widely studied in previous works. As a supplementary study on push-pull dyes, here in this article, 25 push-pull structures comprising electron acceptors derived from indane-1,3-dione and 1H-cyclopenta[b]naphthalene-1,3(2H)-dione (series 1) and 4-dimethoxyphenyl-1-allylidene moieties (series 2) and various electron donors are synthesized and examined as innovative structures for photoinitiation. Among the 2 series of dyes examined in this work and by monitoring the polymerization processes by RT-FTIR measurements, 4 dyes are determined as exhibiting excellent photoinitiation performances and these dyes are selected to perform further studies concerning the chem. mechanisms occurring inside the 3-component PISs, for example, steady state photolysis, fluorescence quenching measurements, and cyclic voltammetry. Markedly, their reactivity is also proved by photoinitiation performance upon sunlight. These results prompt one to develop high performance push-pull dyes as photosensitizers and sunlight can be used as a mild and ecofriendly light source, which can advantageously replace LEDs for the free radical photopolymerization in the future. Finally, the formation of 3-dimensional patterns with an excellent gradient of resolution is successfully achieved by the direct laser write (DLW) with/without SiO2 fillers.

Macromolecular Chemistry and Physics published new progress about 15625-89-5. 15625-89-5 belongs to esters-buliding-blocks, auxiliary class Polymerization Reagents,Crosslinkers, name is Trimethylolpropane triacrylate, and the molecular formula is C17H19N3O7S, Computed Properties of 15625-89-5.

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

Wagener, Tobias’s team published research in Advanced Synthesis & Catalysis in | CAS: 61874-04-2

Advanced Synthesis & Catalysis published new progress about 61874-04-2. 61874-04-2 belongs to esters-buliding-blocks, auxiliary class Benzene,Phenol,Ester,Aldehyde, name is Methyl 2-(3-formyl-4-hydroxyphenyl)acetate, and the molecular formula is C9H8O4, COA of Formula: C10H10O4.

Wagener, Tobias published the artcileSynthesis of Saturated N-Heterocycles via a Catalytic Hydrogenation Cascade, COA of Formula: C10H10O4, the publication is Advanced Synthesis & Catalysis, database is CAplus.

Herein, a one-pot protocol for the synthesis of octahydroindoles I [R1 = H, 3-Me, 6-CF3, etc.], decahydroquinolines II [R2 = H, 7-Me, 6-Et, etc.] and octahydroindolizine III•TsOH through a cascade reaction was presented.

Advanced Synthesis & Catalysis published new progress about 61874-04-2. 61874-04-2 belongs to esters-buliding-blocks, auxiliary class Benzene,Phenol,Ester,Aldehyde, name is Methyl 2-(3-formyl-4-hydroxyphenyl)acetate, and the molecular formula is C9H8O4, COA of Formula: C10H10O4.

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