Category: 4396-13-8

Modak, Arindam; Nandi, Mahasweta; Bhaumik, Asim published the artcile< Titanium containing periodic mesoporous organosilica as an efficient catalyst for the epoxidation of alkenes>, Name: 2,4,6-Trihydroxyisophthalaldehyde, the main research area is titanium periodic mesoporous organosilica catalyst epoxidation alkene.

A new class of titanium containing organic-inorganic hybrid periodic mesoporous organosilica (Ti-LHMS-3) has been synthesized, which contain bis(propyliminomethyl)-phloroglucinol moiety in the pore-wall. The precursor organosilane compound is obtained by Vilsmeier-Haack formylation of phloroglucinol followed by its Schiff base condensation with 3-aminopropyl-triethoxysilane (APTES). The hybrid titananosilicate is finally obtained through in situ condensation of this as-prepared organosilane precursor and tetraethylorthosilicate with titanium isopropoxide under hydrothermal conditions. The material has been thoroughly characterized by using powder X-ray diffraction (PXRD), nitrogen adsorption/desorption, transmission and scanning electron microscopic, and FTIR spectroscopic tools. This hybrid mesoporous titanosilicate material showed excellent catalytic activity in the epoxidation of alkenes under mild liquid phase reaction conditions using tert-Bu hydroperoxide (TBHP) as the oxidant.

Catalysis Today published new progress about Alkenes Role: RCT (Reactant), RACT (Reactant or Reagent). 4396-13-8 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H6O5, Name: 2,4,6-Trihydroxyisophthalaldehyde.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Tran, Duc N.; Cramer, Nicolai published the artcile< Biomimetic Synthesis of (+)-Ledene, (+)-Viridiflorol, (-)-Palustrol, (+)-Spathulenol, and Psiguadial A, C, and D via the Platform Terpene (+)-Bicyclogermacrene>, Quality Control of 4396-13-8, the main research area is biomimetic synthesis ledene viridiflorol palustrol spathulenol psiguadial ACD sesquiterpene; bicyclogermacrene enantioselective synthesis; bicyclogermacrene; biomimetic synthesis; cyclization; natural products; terpenes.

(+)-Bicyclogermacrene (I) is a strained bicyclic and common sesquiterpene found in several essential oils. A short and good yielding synthesis of bicyclogermacrene proceeding in seven steps is reported. This terpene is used as key platform intermediate for a biomimetic access to several aromadendrene sesquiterpenoids, such as ledene, viridiflorol, palustrol, and spathulenol. Furthermore, bicyclogermacrene is shown to be the terpene component in the synthesis of the meroterpenoids psiguadial A, C, and D.

Chemistry – A European Journal published new progress about Biomimetic synthesis. 4396-13-8 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H6O5, Quality Control of 4396-13-8.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Modak, Arindam; Mondal, John; Aswal, Vinod K.; Bhaumik, Asim published the artcile< A new periodic mesoporous organosilica containing diimine-phloroglucinol, Pd(II)-grafting and its excellent catalytic activity and trans-selectivity in C-C coupling reactions>, HPLC of Formula: 4396-13-8, the main research area is phloroglucinol diimine Schiff base palladium complex mesoporous silicate preparation; stereoselective heterogeneous Heck catalyst periodic mesoporous silicate phloroglucinol palladium.

A new organosilane precursor was designed via Vilsmeier-Haack formylation of phloroglucinol followed by its Schiff base condensation with (3-aminopropyl)triethoxysilane (APTES). A novel organic-inorganic hybrid periodic mesoporous organosilica (PMO) LHMS-3 containing the highly coordinating bis(propyliminomethyl)phloroglucinol moiety inside the pore wall was synthesized by using this precursor organosilane mol. Phenolic-OH and imine-N donor sites present in this PMO material were used to anchor Pd(II) species at the surface of the mesopores. Small angle neutron scattering, XRD, HR TEM, SEM, 13C and 29Si solid state MAS NMR, UV-visible and FTIR spectroscopic tools were used to characterize the 2-dimensional-hexagonal mesophase and the presence of the bis(propyliminomethyl)phloroglucinol moiety inside the pore wall. This Pd-anchored material Pd-LHMS-3 showed excellent catalytic activity and trans-selectivity in Heck C-C bond formation reactions for the synthesis of value-added aromatic and aliphatic olefins.

Journal of Materials Chemistry published new progress about Heck reaction (stereoselective). 4396-13-8 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H6O5, HPLC of Formula: 4396-13-8.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Hatzfeld, Jana; Skowaisa, Steffen; Jackel, Elisabeth; Kaufmann, Julia; Haak, Edgar published the artcile< Triaminocyclopentadienyl Ruthenium Complexes - New Catalysts for Cascade Conversions of Propargyl Alcohols>, Related Products of 4396-13-8, the main research area is triaminocyclopentadienyl ruthenium complex preparation catalyst cascade conversion propargyl alc; cycloaddition catalyst triaminocyclopentadienyl ruthenium complex preparation ketolactone phloroglucinol; cyclopentadienyl ligands; heterocycles; homogeneous catalysis; ruthenium; terpenoids.

Various triaminocyclopentadienyl ruthenium complexes have been synthesized from Ru3(CO)12. The new complexes were tested for their ability to catalyze cascade conversions of propargyl alcs. Their associated catalytic activities complement the activities of known diaminocyclopentadienone ruthenium complexes. In particular, the substrate scope of catalytic cycloadditions with 3-ketolactones or phloroglucinol derivatives is extended to terpenoid-derived propargyl alcs. containing an internal alkyne moiety. A wide range of cyclic terpenoid and phloroglucinol adducts are obtained by complementary application of both types of catalysts.

Chemistry – A European Journal published new progress about Alcohols, propargyl Role: RCT (Reactant), RACT (Reactant or Reagent). 4396-13-8 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H6O5, Related Products of 4396-13-8.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Ma, Shuang-Jiang; Yu, Jie; Yan, Da-Wei; Wang, Da-Cheng; Gao, Jin-Ming; Zhang, Qiang published the artcile< Meroterpene-like compounds derived from β-caryophyllene as potent α-glucosidase inhibitors>, Formula: C8H6O5, the main research area is meroterpene derivative preparation beta caryophyllene glucosidase inhibitor antidiabetic agent.

Meroterpenoids isolated from guava (Psidium guajava) and Rhodomyrtus tomentosa possess special skeletons which incorporate terpenoids with phloroglucinol derivatives Most of these meroterpenoids showed high cytotoxicity against cancer cell lines. However, their chem. diversity is very limited. Here, we employed a biomimetic hetero-cycloaddition starting from ortho-quinone methides and an abundant natural product, β-caryophyllene, to generate meroterpene-like compounds Considering that the source plant has hyperglycemic functions, α-glucosidase was selected as a target for bioassay. Nine compounds were screened out for promising activities (IC50 < 15 μM), which were better than the pos. controls, genistein and acarbose. The best inhibitor 12 (IC50 = 2.73 μM) possessed 2 caryophyllene moieties. They represented a new type of skeleton possessing activities against α-glucosidase. The kinetic study exhibited that these inhibitors belong to a non-competitive type. All of these inhibitors may provide an opportunity to develop a new class of antidiabetic agents. Organic & Biomolecular Chemistry published new progress about Antidiabetic agents. 4396-13-8 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H6O5, Formula: C8H6O5.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Bhanja, Piyali; Das, Sabuj K.; Bhunia, Kousik; Pradhan, Debabrata; Hayashi, Taku; Hijikata, Yuh; Irle, Stephan; Bhaumik, Asim published the artcile< A New Porous Polymer for Highly Efficient Capacitive Energy Storage>, Application In Synthesis of 4396-13-8, the main research area is porous polymer supercapacitor electrode capacitance triazine isophthalaldehyde.

The new porous polymer TPDA-1 has been synthesized via solvothermal Schiff base condensation reaction between two organic monomers, i.e., 2,4,6-trihydroxyisophthalaldehyde and 1,3,5-tris(4-aminophenyl)triazine. The TPDA-1 material showed a very high specific capacitance of 469.4 F g-1, at 2 mV s-1 scan rate, together with a high sp. surface area of 545 m2 g-1. It also exhibited excellent cyclic stability with 95% retention of its initial specific capacitance after 1000 cycles at 5 A g-1, suggesting its potential as a high performance supercapacitor. Extended π-conjugation and ion conduction inside the micropores throughout the whole polymeric matrix and high BET surface area could be responsible for this high supercapacitor performance in energy storage device. TPDA-1 has been characterized thoroughly by various electrochem. techniques such as cyclic voltammetry, galvanic charge-discharge, and electrochem. impedance spectroscopy. Our exptl. results suggested a high potential of this porous polymer in energy storage devices for future generation.

ACS Sustainable Chemistry & Engineering published new progress about Aminoplasts Role: PRP (Properties), SPN (Synthetic Preparation), TEM (Technical or Engineered Material Use), PREP (Preparation), USES (Uses). 4396-13-8 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H6O5, Application In Synthesis of 4396-13-8.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Das, Sabuj Kanti; Bhanja, Piyali; Kundu, Sudipta K.; Mondal, Saptarsi; Bhaumik, Asim published the artcile< Role of Surface Phenolic-OH Groups in N-Rich Porous Organic Polymers for Enhancing the CO2 Uptake and CO2/N2 Selectivity: Experimental and Computational Studies>, Electric Literature of 4396-13-8, the main research area is surface phenolic porous carbon dioxide polyamine aminoplast; CO2 uptake; N-rich porous surface; phenolic-OH groups; porous organic polymers; selective CO2/N2 adsorption.

Design and successful synthesis of phenolic-OH and amine-functionalized porous organic polymers as adsorbent for postcombustion CO2 uptake from flue gas mixtures along with high CO2/N2 selectivity is a very demanding research area in the context of developing a suitable adsorbent to mitigate greenhouse gases. Herein, we report three triazine-based porous organic polymers TrzPOP-1, -2, and -3 through the polycondensation of two triazine rings containing tetraamine and three dialdehydes. These porous organic polymers possess high Brunauer-Emmett-Teller (BET) surface areas of 995, 868, and 772 m2 g-1, resp. Out of the three materials, TrzPOP-2 and TrzPOP-3 contain addnl. phenolic-OH groups along with triazine moiety and secondary amine linkages. At 273 K, TrzPOP-1, -2, and -3 displayed CO2 uptake capacities of 6.19, 7.51, and 8.54 mmol g-1, resp., up to 1 bar pressure, which are considerably high among all porous polymers reported till date. Despite the lower BET surface area, TrzPOP-2 and TrzPOP-3 containing phenolic-OH groups showed higher CO2 uptakes. To understand the CO2 adsorption mechanism, we have further performed the quantum chem. studies to analyze noncovalent interactions between CO2 mols. and different polar functionalities present in these porous polymers. TrzPOP-1, -2, and -3 have the capability of selective CO2 uptake over that of N2 at 273 K with the selectivity of 61:1, 117:1, and 142:1 by using the initial slope comparing method, along with 108.4, 140.6, and 167.4 by using ideal adsorbed solution theory (IAST) method, resp. On the other hand, at 298 K, the calculated CO2/N2 selectivities in the initial slope comparing method for TrzPOP-1, -2, and -3 are 27:1, 72:1, and 96:1, whereas those using IAST method are 42.1, 75.7, and 94.5, resp. Cost effective and scalable synthesis of these porous polymeric materials reported herein for selective CO2 capture has a very promising future for environmental clean-up.

ACS Applied Materials & Interfaces published new progress about Activation energy. 4396-13-8 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H6O5, Electric Literature of 4396-13-8.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Mudududdla, Ramesh; Jain, Shreyans K.; Bharate, Jaideep B.; Gupta, Ajai P.; Singh, Baldev; Vishwakarma, Ram A.; Bharate, Sandip B. published the artcile< ortho-Amidoalkylation of phenols via tandem one-pot approach involving oxazine intermediate>, Quality Control of 4396-13-8, the main research area is hydroxybenzyl lactam regioselective preparation; phenol lactam tandem Knoevenagel condensation Diels Alder cycloaddition; perchloric acid amidoalkylation catalyst.

An efficient method for ortho-amidoalkylation of phenols via Mannich-type condensation with formaldehyde and lactams using recyclable solid acid catalyst is described. This is the first report for ortho-amidoalkylation of phenols by lactams via Mannich-type condensation. LC-ESI-MS/MS based mechanistic study revealed that reaction proceeds through o-quinone methide (o-QM) and an oxazine intermediate via tandem Knoevenagel condensation, formal [4 + 2]-Diels-Alder cycloaddition and acid catalyzed oxazine ring-opening.

Journal of Organic Chemistry published new progress about Amidoalkylation. 4396-13-8 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H6O5, Quality Control of 4396-13-8.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Chenavas, Sophie; Fiorini-Puybaret, Christel; Joulia, Philippe; Larrouquet, Camille; Waton, Hugues; Martinez, Agathe; Casabianca, Herve; Fabre, Bernard published the artcile< New formylated phloroglucinol compounds from Eucalyptus globulus foliage>, Related Products of 4396-13-8, the main research area is Eucalyptus formylated phloroglucinol compound acylphloroglucinol.

Two new acylphloroglucinols were isolated from the leaves of Eucalyptus globulus Labill and identified as macrocarpals P (1) and Q (2). Structural elucidations were carried out using conventional 1D and 2D NMR and mass spectrometry together with complementary techniques (UV and IR). Macrocarpal Q was a diastereoisomer of macrocarpal E (3), configuration of which was not precised. Simultaneous isolation of macrocarpals E and Q allowed to determine the configurations of both compounds The diformylphloroglucinol (4) was also isolated as well as already known compounds grandinol, macrocarpals D, I, L, N, O and am-1.

Phytochemistry Letters published new progress about Eucalyptus globulus. 4396-13-8 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H6O5, Related Products of 4396-13-8.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Bharate, Sandip B.; Khan, Shabana I.; Tekwani, Babu L.; Jacob, Melissa; Khan, Ikhlas A.; Singh, Inder Pal published the artcile< S-Euglobals: Biomimetic synthesis, antileishmanial, antimalarial, and antimicrobial activities>, SDS of cas: 4396-13-8, the main research area is euglobal analog preparation antileishmanial antimalarial antimicrobial structure.

Several new euglobal analogs (named as S-euglobals) were synthesized from phloroglucinol using a biomimetic three-component reaction involving Knoevenagel condensation and Diels-Alder cycloaddition with a monoterpene. Newly synthesized euglobal analogs involve monoterpenes that have not yet been encountered in natural euglobals. S-Euglobals along with previously synthesized robustadial A and B were evaluated for in vitro antileishmanial, antimalarial, antimicrobial, and cytotoxic activities. Out of sixteen analogs prepared, nine analogs were found to exhibit antileishmanial activity against Leishmania donovani promastigotes. A 2-carene-derived S-euglobal was the most potent antileishmanial with IC50 of 2.4 μg/mL and IC90 of 8 μg/mL, followed by a second 2-carene-derived S-euglobal and a nopol-derived S-euglobal (IC50 5.5 and 9.5 μg/mL). Antileishmanial activity of robustadial A (5) and B (6) was moderate with IC50 of 20 and 16 μg/mL, resp. Robustadial A and B and a 2-carene-derived S-euglobal exhibited weak antimalarial activity against Plasmodium falciparum (IC50 of 2.7-4.76 μg/mL). Few of the euglobal analogs showed antibacterial activity against methicillin-resistant Staphylococcus aureus. Amongst these, a nopol-derived S-euglobal was the most potent with IC50 of 1.0 μg/mL and MIC of 5.0 μg/mL. Most of the compounds were not cytotoxic up to 25 μg/mL in a panel of cell lines consisting of both cancer (SK-MEL, KB, BT-549, and SK-OV-3) as well as non-cancer kidney (Vero and LLC-PK11) cells.

Bioorganic & Medicinal Chemistry published new progress about Antimalarials. 4396-13-8 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H6O5, SDS of cas: 4396-13-8.

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts