Yu, Longhui’s team published research in Advanced Synthesis & Catalysis in 2022-01-18 | 531-88-4

Advanced Synthesis & Catalysis published new progress about Aryl iodides Role: RCT (Reactant), RACT (Reactant or Reagent). 531-88-4 belongs to class benzofurans, and the molecular formula is C10H10O4, Recommanded Product: 5,6-Dimethoxyisobenzofuran-1(3H)-one.

Yu, Longhui; Liu, Jun; Wang, Hongyu; Xu, Lijun; Wu, Yufei; Zheng, Changwu; Zhao, Gang published the artcile< Asymmetric Dieckmann Condensation towards Spirocyclic Oxindoles Catalyzed by Amino Acid-derived Phosphonium Salts>, Recommanded Product: 5,6-Dimethoxyisobenzofuran-1(3H)-one, the main research area is oxoindolinyl methylbenzenecarboxylate phosphonium salt catalyst enantioselective Dieckmann condensation; spiroindeneoxindole preparation.

An asym. Dieckmann condensation towards spirocyclic oxindoles and aza-oxindoles catalyzed by amino acid-derived phosphonium salt was developed, which expanded the applicability of asym. phosphonium salt catalysis in the production of 1,3-dicarbonyl compounds This reaction was distinguished by its mild conditions (-20°C), low catalyst loading (3-5 mol%), and broad substrate scope (25 examples). Control experiments revealed that both the catalyst’s phosphonium skeleton and H-bonding site were required. Product transformations and a gram scale experiment were also carried out.

Advanced Synthesis & Catalysis published new progress about Aryl iodides Role: RCT (Reactant), RACT (Reactant or Reagent). 531-88-4 belongs to class benzofurans, and the molecular formula is C10H10O4, Recommanded Product: 5,6-Dimethoxyisobenzofuran-1(3H)-one.

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Ibrahimi, Maroua’s team published research in Synlett in 2021-02-28 | 531-88-4

Synlettpublished new progress about Benzaldehydes Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 531-88-4 belongs to class benzofurans, and the molecular formula is C10H10O4, Recommanded Product: 5,6-Dimethoxyisobenzofuran-1(3H)-one.

Ibrahimi, Maroua; Khoumeri, Omar; Abderrahim, Raoudha; Terme, Thierry; Vanelle, Patrice published the artcile< Synthesis of 3-Benzylphthalide Derivatives by Using a TDAE Strategy>, Recommanded Product: 5,6-Dimethoxyisobenzofuran-1(3H)-one, the main research area is benzylphthalide preparation; nitrobenzyl chloride tetrakisdimethylaminoethylene formylbenzoate nucleophilic addition.

A one-pot synthesis of new 3-benzylphthalide derivatives I (X = CH, N; R1 = 4-NO2, 3-OMe-4-NO2, 2-NO2-4-C6H4, etc.; R2 = 4-CN, 5-Cl, 4-COOMe, etc.) was developed by using a strategy based on tetrakis(dimethylamino)ethylene (TDAE). The reactions in the presence of TDAE of substituted benzyl chlorides with Me 2-formylbenzoate or of substituted methyl-2-formylbenzoates with 4-nitrobenzyl chloride furnished the corresponding isobenzofuran-1(3H)-one products in moderate to good yields.

Synlettpublished new progress about Benzaldehydes Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 531-88-4 belongs to class benzofurans, and the molecular formula is C10H10O4, Recommanded Product: 5,6-Dimethoxyisobenzofuran-1(3H)-one.

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Li, Junxuan’s team published research in Science China: Chemistry in 2022-01-31 | 531-88-4

Science China: Chemistrypublished new progress about Alcohols Role: RCT (Reactant), RACT (Reactant or Reagent). 531-88-4 belongs to class benzofurans, and the molecular formula is C10H10O4, Category: benzofurans.

Li, Junxuan; Zhou, Jinlei; Wang, Yumei; Yu, Yue; Liu, Qiang; Yang, Tilong; Chen, Huoji; Cao, Hua published the artcile< Mechanistic insight into the synergistic Cu/Pd-catalyzed carbonylation of aryl iodides using alcohols and dioxygen as the carbonyl source>, Category: benzofurans, the main research area is aryl iodide alc carbonylation dioxygen carbonyl source mechanistic insight.

Pd-catalyzed carbonylation, as an efficient synthetic approach for the installation of carbonyl groups in organic compounds, has been one of the most important research fields in the past decade. Although elegant reactions that allow highly selective carbonylations have been developed, straightforward routes with improved reaction activity and broader substrate scope remain long-term challenges for new practical applications. Here, authors show a new type of synergistic Cu/Pd-catalyzed carbonylation reaction using alcs. and dioxgen as the carbonyl sources. A broad range of aryl iodides and alcs. are compatible with this protocol. The reaction is concise and practical due to the ready availability of the starting materials and the scalability of the reaction. In addition, the reaction affords lactones and lactams in an intermol. fashion. Moreover, DFT calculations have been performed to study the detailed mechanisms.

Science China: Chemistrypublished new progress about Alcohols Role: RCT (Reactant), RACT (Reactant or Reagent). 531-88-4 belongs to class benzofurans, and the molecular formula is C10H10O4, Category: benzofurans.

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Liu, Bin’s team published research in Chinese Chemical Letters in 2019-03-31 | 531-88-4

Chinese Chemical Letterspublished new progress about Bases Role: RGT (Reagent), RACT (Reactant or Reagent). 531-88-4 belongs to class benzofurans, and the molecular formula is C10H10O4, Recommanded Product: 5,6-Dimethoxyisobenzofuran-1(3H)-one.

Liu, Bin; Zhou, Xigeng published the artcile< Synthesis of 1,2-phenylenedimethanols by base-promoted reduction of isobenzofuran-1(3H)-ones with silane>, Recommanded Product: 5,6-Dimethoxyisobenzofuran-1(3H)-one, the main research area is phenylenedimethanol preparation isobenzofuranone reduction base silane.

An efficient method for preparation of substituted 1,2-phenylenedimethanols and aliphatic 1,4-diols that are valuable intermediates in organic synthesis, was developed by the base-promoted reduction of isobenzofuran-1(3H)-ones and γ-lactones with silane under mild conditions. Compared with traditional procedures using stoichiometric amounts of metal hydrides and alkyl reductants, the present method avoids the use of sensitive reagents and is operationally simple and a broad variety of functional groups are tolerated.

Chinese Chemical Letterspublished new progress about Bases Role: RGT (Reagent), RACT (Reactant or Reagent). 531-88-4 belongs to class benzofurans, and the molecular formula is C10H10O4, Recommanded Product: 5,6-Dimethoxyisobenzofuran-1(3H)-one.

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Lei, Zhen-Yao’s team published research in Organic & Biomolecular Chemistry in 2022 | 531-88-4

Organic & Biomolecular Chemistrypublished new progress about Amides Role: RCT (Reactant), RACT (Reactant or Reagent) (alkenyl). 531-88-4 belongs to class benzofurans, and the molecular formula is C10H10O4, Reference of 531-88-4.

Lei, Zhen-Yao; Hu, Kui; He, Yuan-Xiang; Geng, Shu; Chen, Li-Na; Zou, Shuai; Pan, Li; Ding, Zhi-Jun; Huang, Feng published the artcile< Visible light-induced N-radical 5-exo/6-endo cyclization of alkenyl amides: facile access to isoindolinones/isoquinolinones>, Reference of 531-88-4, the main research area is isoindolinone isoquinolinone preparation; alkenyl amide visible light radical cyclization.

An efficient N-centered radical intramol. cyclization reaction of alkenyl amides induced by visible light was described. In this process, an alkenyl amide underwent 5-exo/6-endo cyclization to selectively yield two critical alkaloid structures, namely isoindolinones and isoquinolinones.

Organic & Biomolecular Chemistrypublished new progress about Amides Role: RCT (Reactant), RACT (Reactant or Reagent) (alkenyl). 531-88-4 belongs to class benzofurans, and the molecular formula is C10H10O4, Reference of 531-88-4.

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Learn more about cas: 38103-06-9 | Anti-Corrosion Methods and Materials 2019

5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione)(cas: 38103-06-9) is a diallyl based epoxy modification agent that blends with the resin to improve the mechanical property of the epoxy material.Electric Literature of C31H20O8 It is majorly used in novalac based resins, which can be further cured with bismaleimides (BMI) for aerospace, electronics and wireless communication based applications.

Malav, Jeetendra Kumar;Rathod, Ramesh C.;Tandon, Vipin;Patil, Awanikumar P. published 《Enhancement of corrosion protection of low nickel austenitic stainless steel by electroactive polyimide-CuO composites coating in chloride environment》 in 2019. The article was appeared in 《Anti-Corrosion Methods and Materials》. They have made some progress in their research.Electric Literature of C31H20O8 The article mentions the following:

The purpose of this study is to improve the anticorrosion performance of low nickel stainless steel (AISI 201) in 3.5% NaCl by electroactive polyimide/copper oxide (EPI/CuO) composites coating. Design/methodol./approach: Electroactive polyimide/copper oxide (EPI/CuO) composites were prepared by oxidative coupling polymerization followed by thermal imidization method. The functional and structural properties of composites were characterized by X-ray diffraction, Fourier transmission infra-red and ultra violet-visible spectroscopy and the surface topog. was characterized by field emission scanning electron microscope anal. and anticorrosion performance in 3.5 Weight% NaCl was evaluated by electrochem. techniques. The obtained results of electrochem. techniques measurement indicated that the composites coated samples give better corrosion protection against attacking electrolyte. The ever-increasing price of nickel (Ni) is driving the industries to use low-Ni austenitic stainless steels (ASSs). However, it exhibits relatively poor corrosion resistance as compared with conventional Cr-Ni ASSs. Nonetheless, its corrosion resistance can be enhanced by polymeric (electroactive polyimide [EPI]) coating. CuO particles exhibit the hydrophobic properties and can be used as inorganic filler to incorporate in EPI to further enhance the corrosion protection. The present research paper is beneficial for industries to use low-cost AISI 201, enhance its corrosion resistance and replace the use of costly conventional Cr-Ni ASSs. The experimental procedure involved many compounds, such as 5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione) (cas: 38103-06-9) .

5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione)(cas: 38103-06-9) is a diallyl based epoxy modification agent that blends with the resin to improve the mechanical property of the epoxy material.Electric Literature of C31H20O8 It is majorly used in novalac based resins, which can be further cured with bismaleimides (BMI) for aerospace, electronics and wireless communication based applications.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

New progress of cas: 38103-06-9 | Fibers and Polymers 2022

5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione)(cas: 38103-06-9) is a diallyl based epoxy modification agent that blends with the resin to improve the mechanical property of the epoxy material.COA of Formula: C31H20O8 It is majorly used in novalac based resins, which can be further cured with bismaleimides (BMI) for aerospace, electronics and wireless communication based applications.

Yin, Lu-meng;Yang, Ming-wei;Liu, Quan;Li, Xiang;Zhang, Yan;Zhi, Xin-Xin;Qi, Hao-ran;Liu, Jin-gang;Lv, Feng-zhu published 《Electrospun Polyimide Ultrafine Non-woven Fibrous Membranes Containing Phenyl-substituted Quinoxaline Units with Improved Hydrolysis Resistance for Potential Applications in High-temperature Water Environments》 in 2022. The article was appeared in 《Fibers and Polymers》. They have made some progress in their research.COA of Formula: C31H20O8 The article mentions the following:

Two organo-soluble polyimide resins containing phenyl-substituted quinoxaline units (PIPQ) were successfully prepared via the two-step chem. imidization procedure from an aromatic diamine, 6(7)-amino-2-(4-aminophenyl)-3-phenylquinoxaline (PQDA) and aromatic dianhydrides with flexible mol. structures. The derived PIPQ-1 resin from PQDA and 4,4′-(hexafluoroisopropylidene)diphthalic anhydride (6FDA) and the PIPQ-2 resin from PQDA and 2,2-bis[4-(3,4-dicarboxyphenoxy)phenyl]propane dianhydride (BPADA) were all soluble in polar aprotic solvents, such as N-methyl-2-pyrrolidone (NMP) and N,N-dimethylacetamide (DMAc). The PIPQ/DMAc solutions with the solid contents of 25-35 wt% were used as the starting mediums and the PIPQ ultrafine non-woven fibrous membranes (UFMs) were successfully prepared by the one-step electrospinning (ES) procedure. The fabricated PIPQ UFMs exhibited good thermal stability with the 5% weight loss temperatures (T5%) of 537°C for PIPQ-1 (6FDA-PQDA) and 517°C for PIPQ-2 (BPADA-PQDA) in nitrogen, resp. In addition, the PIPQ UFMs exhibited glass transition temperatures (Tg) higher than 252°C. The PIPQ UFMs survived even during the aging in boiling aqueous sodium hydroxide solution (concentration: 20 wt%) for 3 h while the PI-ref UFM totally hydrolyzed during the test. And 5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione) (cas: 38103-06-9) was used in the research process.

5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione)(cas: 38103-06-9) is a diallyl based epoxy modification agent that blends with the resin to improve the mechanical property of the epoxy material.COA of Formula: C31H20O8 It is majorly used in novalac based resins, which can be further cured with bismaleimides (BMI) for aerospace, electronics and wireless communication based applications.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Polymer | Cas: 38103-06-9 was involved in experiment

5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione)(cas: 38103-06-9) is a diallyl based epoxy modification agent that blends with the resin to improve the mechanical property of the epoxy material.Application of 38103-06-9 It is majorly used in novalac based resins, which can be further cured with bismaleimides (BMI) for aerospace, electronics and wireless communication based applications.

Wolfgang, Josh D.;Reynolds, Karina J.;Arrington, Clay B.;Odle, Roy R.;Nazarenko, Sergei I.;Long, Timothy E. published 《Influence of dianhydride regiochemistry on thermomechanical and rheological properties of 3,3′- and 4,4′-polyetherimides》 in 2021. The article was appeared in 《Polymer》. They have made some progress in their research.Application of 38103-06-9 The article mentions the following:

The design of linear high performance polyetherimides (PEIs) comprising 3,3′- and 4,4′-bisphenol-A dianhydride (bis-DA) and m-phenylene diamine (mPD) provided an opportunity to elucidate the influence of dianhydride regiochem. on thermomech. and rheol. properties. This unique pair of regioisomers allowed the tuning of the thermal and rheol. properties for high glass transition temperature polyimides for emerging engineering applications. Step-growth polycondensation enabled the production of high mol. weight PEIs for subsequent thermal and mech. anal. Monofunctional phthalic anhydride as an endcapper and monomeric stoichiometric imbalances enabled predictable number-average mol. weights ranging from 3600 to 35,400 g mol-1, as confirmed with size exclusion chromatog. coupled with light scattering detection for absolute mol. weight determination The selection of the dianhydride regioisomer influenced the weight loss profile as a function of temperature, entanglement mol. weight (Me), glass transition temperature (Tg), tensile strain-at-break, zero-shear melt viscosity, average hole-size free volume (Vh), and the plateau modulus prior to viscous flow during dynamic mech. anal. The 3,3′- PEI composition interestingly exhibited a ∼20°C higher glass transition temperature than the corresponding 4,4′- PEI analog. Moreover, melt rheol. anal. revealed a two-fold increase in Me for 3,3′- PEI, which pointed to the origin of the differences in mech. and rheol. properties as a function of PEI backbone geometry. To complete the study, the researchers used 5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione) (cas: 38103-06-9) .

5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione)(cas: 38103-06-9) is a diallyl based epoxy modification agent that blends with the resin to improve the mechanical property of the epoxy material.Application of 38103-06-9 It is majorly used in novalac based resins, which can be further cured with bismaleimides (BMI) for aerospace, electronics and wireless communication based applications.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Wu, Yancheng et al. published new progress in experiments with the help of cas: 38103-06-9

5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione)(cas: 38103-06-9) is a diallyl based epoxy modification agent that blends with the resin to improve the mechanical property of the epoxy material.Recommanded Product: 38103-06-9 It is majorly used in novalac based resins, which can be further cured with bismaleimides (BMI) for aerospace, electronics and wireless communication based applications.

Wu, Yancheng;Ji, Jingqi;Huang, Haohao;Liu, Shumei;Zhao, Jianqing published 《Facile synthesis of acyloxy-containing fluorene-based Cardo polyimides with high optical transparency, fluorescence and low dielectric constant》. The research results were published in《Reactive & Functional Polymers》 in 2021.Recommanded Product: 38103-06-9 The article conveys some information:

A series of acyloxy-containing fluorene-based Cardo polyimides (PIs) were facilely synthesized by the post-polymerization modification based on a simple esterification of hydroxyl-containing PIs. Incorporation of acyloxy groups may reduce the packing d. of PI chains and weaken both inter- and intra-chain charge transfer complexes (CTC) formation. Accordingly, the modified PIs exhibit the improved solubility in low-boiling-point solvents and optical transparence. The optical transmittance at 400 nm (T400) of all modified PI films is significantly increased to 80.1-83.5% from 41.6-54.5% of the precursor PI films. Meanwhile, the modified PI films exhibit a bright fluorescence. The modified PIs still display the superior heat resistance with a glass transition temperature (Tg) of 301.1-390.9°C as well as admirable mech. properties with a tensile strength (TS) of 72.1-81.3 MPa. In addition, the dielec. constant (k) value at 1 MHz of the modified PI films is decreased to 2.58-2.90 from 3.95-4.48 of the precursor PI films, which is attributed to the enlarged free volume and reduced water absorption afforded by the incorporation of acyloxy groups. This work provides an efficient post-polymerization modification approach to simultaneously affording the multifunctional PI films with high Tg, high T400 and low k, probably as the potential candidates for the practical application in display and microelectronic industries. The experimental procedure involved many compounds, such as 5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione) (cas: 38103-06-9) .

5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione)(cas: 38103-06-9) is a diallyl based epoxy modification agent that blends with the resin to improve the mechanical property of the epoxy material.Recommanded Product: 38103-06-9 It is majorly used in novalac based resins, which can be further cured with bismaleimides (BMI) for aerospace, electronics and wireless communication based applications.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

New progress of cas: 38103-06-9 | ACS Nano 2021

5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione)(cas: 38103-06-9) is a diallyl based epoxy modification agent that blends with the resin to improve the mechanical property of the epoxy material.Application of 38103-06-9 It is majorly used in novalac based resins, which can be further cured with bismaleimides (BMI) for aerospace, electronics and wireless communication based applications.

Application of 38103-06-9《Polyimide Aerogel Fibers with Superior Flame Resistance, Strength, Hydrophobicity, and Flexibility Made via a Universal Sol-Gel Confined Transition Strategy》 was published in 2021. The authors were Li, Xin;Dong, Guoqing;Liu, Zengwei;Zhang, Xuetong, and the article was included in《ACS Nano》. The author mentioned the following in the article:

Aerogel fibers with ultrahigh porosity, large sp. surface area, and ultralow d. have shown increasing interest due to being considered as the next generation thermal insulation fibers. However, it is still a great challenge to fabricate arbitrary aerogel fibers via the traditional wet-spinning approach due to the obvious conflict between the static sol-gel transition of the aerogel bulks and the dynamic wet-spinning process of aerogel fibers. Herein, a sol-gel confined transition (SGCT) strategy was developed for fabricating various mesoporous aerogel fibers, in which the aerogel precursor solution was first driven by the surface tension into the capillary tubes, then the gel fibers were easily formed in the confined space after static sol-gel process, and finally the mesoporous aerogel fibers were obtained via the supercritical CO2 drying process. As a typical case, the polyimide (PI) aerogel fiber prepared via the SGCT approach has exhibited a large sp. surface area (up to 364 m2/g), outstanding mech. property (with elastic modulus of 123 MPa), superior hydrophobicity (with contact angle of 153°), and excellent flexibility (with curvature radius of 200μm). Therefore, the aerogel woven fabric made from PI aerogel fibers has possessed an excellent thermal insulation performance in a wide temperature window, even under the harsh environment. Besides, arbitrary kinds of aerogel fibers, including organic aerogel fibers, inorganic aerogel fibers, and organic-inorganic hybrid aerogel fibers, have been fabricated successfully, suggesting the universality of the SGCT strategy, which not only provides a way for developing aerogel fibers with different components but also plays an irreplaceable role in promoting the upgrading of the fiber fields.5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione) (cas: 38103-06-9) were involved in the experimental procedure.

5,5′-((Propane-2,2-diylbis(4,1-phenylene))bis(oxy))bis(isobenzofuran-1,3-dione)(cas: 38103-06-9) is a diallyl based epoxy modification agent that blends with the resin to improve the mechanical property of the epoxy material.Application of 38103-06-9 It is majorly used in novalac based resins, which can be further cured with bismaleimides (BMI) for aerospace, electronics and wireless communication based applications.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem