Day: November 21, 2022

Fernandes, Alessandra A. G. published the artcileGeneral Platform for the Conversion of Isoxazol-5-ones to 3,5-Disubstituted Isoxazoles via Nucleophilic Substitutions and Palladium Catalyzed Cross-Coupling Strategies, Formula: C9H7NO2, the publication is European Journal of Organic Chemistry (2019), 2019(19), 3022-3034, database is CAplus.

A general platform for the conversion of isoxazol-5-ones to 3,5-disubstituted isoxazoles has been developed via a two-step strategy. The first step leads to the formation of 5-(pseudo)halogenated isoxazoles, while in the second, a variety of heteroalkyl-, heteroaryl-, alkyl-, alkenyl-, alkynyl- and aryl-chains can be installed via nucleophilic substitutions or palladium catalyzed cross-coupling reactions.

European Journal of Organic Chemistry published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C9H7NO2, Formula: C9H7NO2.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Altieri, Elisa published the artcileAn improved diastereoselective synthesis of spiroazoles using multi-component domino transformations, Formula: C9H7NO2, the publication is Synlett (2010), 2106-2108, database is CAplus.

Spiroisoxazole and spiropyrazole derivatives were obtained in a four-component reaction of active isoxazol- or pyrazol-5-ones with aromatic aldehydes, phenacyl chloride and AcOH-AcONH₄ mixture The reaction sequence is highly chemo- and diastereoselective affording good yields of spiroisoxazoles in refluxing ethanol, while efficient formation of spiropyrazoles is closely related to the use of a microwave-assisted protocol.

Synlett published new progress about 1076-59-1. 1076-59-1 belongs to isoxazole, auxiliary class Oxazoline,Benzene,Ester, name is 3-Phenylisoxazol-5(2H)-one, and the molecular formula is C9H7NO2, Formula: C9H7NO2.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Pan, Jiunn-Hung published the artcileTheoretical Investigation of Organic Amines as Hole Transporting Materials: Correlation to the Hammett Parameter of the Substituent, Ionization Potential, and Reorganization Energy Level, Safety of 9-(4-Fluorophenyl)-9H-carbazole, the publication is Australian Journal of Chemistry (2009), 62(5), 483-492, database is CAplus.

Theor. calculations on organic amines widely used as hole-transporting materials (HTMs) in multilayer organic light-emitting diodes have been performed. The calculated I_p and the reorganization energy for hole transport (λ₊) of triphenylamine (TPA), 9-phenyl-9H-carbazole (PC), and their derivatives, are found to be related to their Hammett parameter (σ). In this study, the d. functional theory (DFT) calculation is used to optimize 82 TPA and PC derivatives Electronic structures of these compounds in the neutral and the radical-cation states are obtained based on calculations on optimized geometrical structures. The I_p and λ₊ values are derived from calculated heats of formation (or total energy) of the neutral and the radical-cation states. In particular, the calculated I_ps for these derivatives correlate well with the exptl. data. The substitution effect for the mono-substituted TPA and PC is displayed in that the I_ps of the TPA and PC derivatives with electron-donating and -withdrawing substituents are lower and higher than those of TPA and PC, resp. For the effect of substitution position, the para-substituted TPA derivatives have higher I_p and -E^HOMO than those of meta-substituted TPAs. The substitution effects in di- and tri-substituted TPAs are more pronounced than that of mono-substituted ones. According to the results, the calculated I_ps shows an excellent agreement with the exptl. oxidation potentials (E_P/2) in these TPA derivatives Furthermore, these calculation results can be employed to predict electro-luminescent properties for new and improved HTMs.

Australian Journal of Chemistry published new progress about 57103-14-7. 57103-14-7 belongs to isoxazole, auxiliary class Fused Tricycles,Carbazoles, name is 9-(4-Fluorophenyl)-9H-carbazole, and the molecular formula is C18H12FN, Safety of 9-(4-Fluorophenyl)-9H-carbazole.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Chen, Jiang published the artcileInfluence of flurbiprofen and parecoxib sodium on behavior and spinal cord COX-2 expression in incision pain rats, Category: isoxazole, the publication is Zhongguo Yaowu Yu Linchuang (2014), 14(5), 600-601, database is CAplus.

Forty-eight SD rats were randomly divided into control group, 0.9% NaCl group, flurbiprofen group (0.9 mg/100 g) and parecoxib sodium group (0.6 mg/100 g). Behavior and pain score were observed COX-2 expression was determined by ELISA. Pain score and COX-2 expression of flurbiprofen group and parecoxib sodium group were significantly lower than those in NaCl group (P<0.05). And no significant difference of Pain score and COX-2 expression was found between flurbiprofen group and parecoxib sodium group (P>0.05). Flurbiprofen and parecoxib sodium both inhibits COX-2 expression in spinal cord and showed analgesic effect in incision pain rats.

Zhongguo Yaowu Yu Linchuang published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C19H17N2NaO4S, Category: isoxazole.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Cui, Xi-shun published the artcileDevelopment and Validation of the Production Process of Parecoxib Sodium Freeze-dried Preparation Based on Quality by Design, Application of Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, the publication is Zhongguo Yaoxue Zazhi (Beijing, China) (2017), 52(15), 1337-1341, database is CAplus.

To prepare parecoxib sodium freeze-dried preparation, evaluate and validate the feasibility of the production process and quality reliability of the preparation Risk assessment of the production process of parecoxib sodium freeze-dried preparation was performed based on the method of quality by design (QbD). The key steps and key process parameters were identified. The critical quality attributes (CQAs)of the intermediates and final product were clarified, the validation protocol and acceptable standard were accordingly developed, and the production process was validated. The production process of parecoxib sodium freeze-dried preparation met the GMP requirements, and the intermediate and final products met the quality standards The established production process of pareeoxib sodium freeze-dried preparation is feasible and the product quality is controllable.

Zhongguo Yaoxue Zazhi (Beijing, China) published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C19H17N2NaO4S, Application of Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Liu, Xiao-Ke published the artcilePrediction and Design of Efficient Exciplex Emitters for High-Efficiency, Thermally Activated Delayed-Fluorescence Organic Light-Emitting Diodes, Formula: C33H22N4, the publication is Advanced Materials (Weinheim, Germany) (2015), 27(14), 2378-2383, database is CAplus and MEDLINE.

3 Exciplex emitter materials were designed by 50-50% mixing 3 hole-transporting arylamines with a High-T₁ bipolar host. The 3 exciplex emitters show broad and notably red-shifted emission relative to those of the constituting mols. High-T₁ constituting mols. are preferable for designing exciplex emitters with high fluorescence efficiency because the high T₁ of the constituting mols. prevent energy leakage and enable efficient reverse intersystem crossing.

Advanced Materials (Weinheim, Germany) published new progress about 1313391-57-9. 1313391-57-9 belongs to isoxazole, auxiliary class OLED Materials,Red Fluorescence Dopants, name is 3-(4,6-Diphenyl-1,3,5-triazin-2-yl)-9-phenyl-9H-carbazole, and the molecular formula is C33H22N4, Formula: C33H22N4.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Liu, Xiao-Ke published the artcileNearly 100% Triplet Harvesting in Conventional Fluorescent Dopant-Based Organic Light-Emitting Devices Through Energy Transfer from Exciplex, Category: isoxazole, the publication is Advanced Materials (Weinheim, Germany) (2015), 27(12), 2025-2030, database is CAplus and MEDLINE.

A simple approach for nearly 100% triplet harvesting in conventional fluorescent dopant-based organic LEDs through energy transfer from exciplex is proposed. This approach was realized by (a) using a thermally-activated delayed fluorescence exciplex host to up-convert the triplet excitons to the S₁; (b) using an exciplex host with its HOMO and LUMO close to those of the fluorescent dopant to minimize exciton trapping; (c) using an extremely low dopant concentration to minimize triplet-triplet energy transfer from the host to the dopant. Based on this design, the best C545T-doped device employing TAPC:DPTPCz as host shows a low turn-on voltage of 2.8 V and maximum CE, PE, and EQE of 44.0 cd A^-1, 46.1 lm W^-1, and 14.5%, resp. This approach probably is a general strategy easily extendable to other exciplex host:fluorescent dopant systems.

Advanced Materials (Weinheim, Germany) published new progress about 1313391-57-9. 1313391-57-9 belongs to isoxazole, auxiliary class OLED Materials,Red Fluorescence Dopants, name is 3-(4,6-Diphenyl-1,3,5-triazin-2-yl)-9-phenyl-9H-carbazole, and the molecular formula is C33H22N4, Category: isoxazole.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Qiu, Liang-cheng published the artcileEffects of preemptive parecoxib sodium versus flurbiprofen axetil on blood coagulation, Application of Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, the publication is Linchuang Mazuixue Zazhi (2014), 30(11), 1087-1090, database is CAplus.

The effects of preemptive parecoxib sodium and flurbiprofen axetil on blood coagulation in patients undergoing radical mastectomy for breast cancer were compared. Ninety patients undergoing selective radical mastectomy were randomly allocated to three groups: 30 were injected with parecoxib sodium 40 mg (group P), 30 with flurbiprofen axetil 50 mg (group F) and 30 with normal saline (group N), each 10 mL during 10 min before induction of anesthesia. Total i.v. target-controlled infusion of remifentanil and propofol was used for anesthesia. Normal saline was the only liquid during operation. Three groups received patient controlled i.v. analgesia (PCIA) with sufentanil after surgery. Venous blood samples were taken from upper extremity before and at 30 min, 1 h, 3 h and 6 h after parecoxib, flurbiprofen axetil or normal saline administration for coagulation test, platelet count (Plt) and platelet aggregation rate (PAR), and the adverse reactions were recorded during 24 h after surgery. After 30 min of drugs administration, thrombin time (TT) of three groups was significantly extend (P<0.05); and fibrinogen (Fib) of groups F and N reduced significantly (P<0.05), which was significantly lower than that of group P (P<0.05). There were no significant differences between the other time points of coagulation parameters, Plt and PAR. The incidences of nausea arid vomiting within 24 h after surgery in groups P and F were reduced significantly compared with group N (P<0.05), the incidences of dizziness, sweating and itching had no differences, and there were no adverse reactions of gastrointestinal bleeding/ulcers and respiratory depression in all there groups. As to 50 mg of flurbiprofen axetil, preemptive parecoxib sodium 40 mg can temporarily enhance blood coagulation in patients undergoing radical mastectomy for breast cancer.

Linchuang Mazuixue Zazhi published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C19H17N2NaO4S, Application of Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Ding, Xian published the artcileEffects of early use of parecoxib sodium on serum TNF-α in mice with burn, Recommanded Product: Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, the publication is Jiangsu Yiyao (2015), 41(21), 2514-2516, C2, database is CAplus.

Objective To observe the effects of early use of parecoxib sodium on serum tumor necrosis factor-α(TNF-α) in mice with burn. Methods Two hundreds ICR male mice were randomly divided into 4 groups with 50 mice each. At 4 h after the burn models were established, the mice were i.p. injected with normal saline (group IU), parecoxib sodium 0.75 mg/kg (group TA) or parecoxib sodium 7.5 mg/kg (group TB), which was repeated at 24 and 48 h after the first injection. The mice without burn were taken as the controls (group U). Serum levels of TNF-α were detected by CBA liquid chip method at 6(T1), 12(T2), 24(T3), 48(T4) and 72 h (T5) after the first injection. Results Compared with group U, serum concentration of TNF-α in group IU at each time point was increased significantly (P<0.05). Serum level of TNF-α at T1 were higher in group TA than that in group U (P<0.05). Serum levels of TNF-α at T2-T5 were lower in group TB than those in group U (P<0.05). Serum levels of TNF-α at T2-T5 in group TA and at T1-T5 in group TB were lower than those in group IU (P<0.05). Conclusion The application of parecoxib sodium 0.75 mg/kg in the early stage of burn can moderately decrease serum concentration of TNF-α, which is beneficial to inhibiting inflammation in mice with burn. But the use of parecoxib sodium 7.5 mg/kg may decrease serum concentration of TNF-α excessively, which is not beneficial to keeping the rebalance of proinflammatory cytokines and anti-inflammatory cytokines.

Jiangsu Yiyao published new progress about 198470-85-8. 198470-85-8 belongs to isoxazole, auxiliary class Immunology/Inflammation,COX, name is Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide, and the molecular formula is C19H17N2NaO4S, Recommanded Product: Sodium ((4-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)(propionyl)amide.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem

Zhang, Jinfeng published the artcileOrganic nanostructures of thermally activated delayed fluorescent emitters with enhanced intersystem crossing as novel metal-free photosensitizers, Product Details of C33H22N4, the publication is Chemical Communications (Cambridge, United Kingdom) (2016), 52(79), 11744-11747, database is CAplus and MEDLINE.

We applied organic nanostructures based on thermally activated delayed fluorescent (TADF) emitters for singlet oxygen generation. Due to the extremely small energy gaps between the excited singlet states (S₁) and triplet states (T₁) of these heavy-metal-free organic nanostructures, intersystem conversion between S₁ and T₁ can occur easily. This strategy also works well for exciplex-type TADF emitters prepared by mixing suitable donors and acceptors which have no TADF characteristics themselves.

Chemical Communications (Cambridge, United Kingdom) published new progress about 1313391-57-9. 1313391-57-9 belongs to isoxazole, auxiliary class OLED Materials,Red Fluorescence Dopants, name is 3-(4,6-Diphenyl-1,3,5-triazin-2-yl)-9-phenyl-9H-carbazole, and the molecular formula is C12H9NO, Product Details of C33H22N4.

Referemce:
https://en.wikipedia.org/wiki/Isoxazole,
Isoxazole | C3H3NO – PubChem