Category: 123-11-5

Safety of 4-Methoxybenzaldehyde. Authors Zeid, SB; Hamade, A; Najjar, F; Carreaux, F; Eid, S in SPRINGER INTERNATIONAL PUBLISHING AG published article about in [Zeid, Samar Bou; Hamade, Aline; Najjar, Fadia; Eid, Samar] Lebanese Univ, Fac Sci 2, Dept Biol Chem & Biochem, Lab Innovat Therapeut, Fanar, Lebanon; [Zeid, Samar Bou; Carreaux, Francois] Univ Rennes 1, CNRS, ISCR, UMR 6226, 263 Ave Gen Leclerc,Campus Beaulieu, F-35000 Rennes, France in 2021, Cited 43. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

Herein we describe the synthesis of five new 2-aryl and 2-alkylimidazolone derivatives via an effective one-pot synthetic strategy assisted by microwave irradiations which allowed us to access the desired product in a reduced time reaction compared to the thermal heating and a slightly better yield (48% compared to 45%). The new imidazolone derivatives were evaluated for their anticancer activity in vitro against MCF-7, MDA-MB-231 and HepG2 cell lines. The results showed good cytotoxic effects for some of these derivatives on both MCF-7 and HepG2 cell lines in the range of 5.7-11.3 mu M. Among the synthesized derivatives, 2ab and 2b showed the strongest activity with IC50 values of 7 and 5.7 mu M (MCF-7) and 6.2 and 8.6 mu M (HepG2), respectively. The cytotoxic activities of these derivatives were moderate compared to those of doxorubicin. However, this product showed higher toxicity in vivo on the development of zebrafish embryos than the synthesized imidazolones. These derivatives at high concentrations exhibited some morphological abnormalities on the embryos.

Safety of 4-Methoxybenzaldehyde. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Zeid, SB; Hamade, A; Najjar, F; Carreaux, F; Eid, S or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Ultrasound promoted and Kit-6 mesoporous silica-supported Fe3O4 magnetic nanoparticles catalyzed cyclocondensation reaction of 4-hydroxycoumarin, 3,4-methylenedioxyphenol, and aromatic aldehydes WOS:000604548400001 published article about POT MULTICOMPONENT SYNTHESIS; ACIDIC IONIC LIQUID; GREEN SYNTHESIS; 3-COMPONENT SYNTHESIS; RECOVERABLE CATALYST; TIO2 NANOPARTICLES; EFFICIENT; DERIVATIVES; NANOCOMPOSITE; FE3O4-AT-SIO2-AT-KIT-6 in [Abdolmohammadi, Shahrzad] Islamic Azad Univ, East Tehran Branch, Dept Chem, POB 18735-138, Tehran, Iran; [Shariati, Shahab] Islamic Azad Univ, Rasht Branch, Dept Chem, Rasht, Iran; [Mirza, Behrooz] Islamic Azad Univ, Karaj Branch, Dept Chem, Karaj, Iran in 2021, Cited 80. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5. Computed Properties of C8H8O2

A new effective approach to synthesize a series of 7-aryl-6H,7H-[1]benzopyrano[4,3-b][1,3]dioxolo[4,5-g][1]benzopyran-6-ones was reported using Fe3O4@SiO2@Kit-6 as heterogeneous catalyst at room temperature under ultrasonic irradiation in aqueous media. This procedure is of great value due to its short reaction time, high yields, simple processing, and the use of easily available and magnetically recyclable heterogeneous catalyst.

Computed Properties of C8H8O2. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Abdolmohammadi, S; Shariati, S; Mirza, B or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Li, XD; Golz, C; Alcarazo, M in [Li, Xiangdong; Golz, Christopher; Alcarazo, Manuel] Georg August Univ Gottingen, Inst Organ & Biomol Chem, Tammannstr 2, D-37077 Gottingen, Germany published alpha-Diazo Sulfonium Triflates: Synthesis, Structure, and Application to the Synthesis of 1-(Dialkylamino)-1,2,3-triazoles in 2021, Cited 88. Computed Properties of C8H8O2. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.

The one-pot synthesis of a series of sulfonium salts containing transferable diazomethyl groups is described, and the structure of these compounds is elucidated by X-ray crystallography. Under photochemical conditions, reaction of these salts with N,N-dialkyl hydrazones affords 1-(dialkylamino)-1,2,3-triazoles via diazomethyl radical addition to the azomethine carbon followed by intramolecular ring closure. The straightforward transformation of the structures thus obtained into mesoionic carbene-metal complexes is also reported and the donor properties of these new ligands characterized.

Computed Properties of C8H8O2. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Li, XD; Golz, C; Alcarazo, M or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Application In Synthesis of 4-Methoxybenzaldehyde. Authors Nguyen, VT; Nguyen, HT; Tran, PH in ROYAL SOC CHEMISTRY published article about in [Nguyen, Vu Thanh; Nguyen, Hai Truong; Tran, Phuong Hoang] Univ Sci, Dept Organ Chem, Fac Chem, Ho Chi Minh City 721337, Vietnam; [Nguyen, Vu Thanh; Nguyen, Hai Truong; Tran, Phuong Hoang] Vietnam Natl Univ, Ho Chi Minh City 721337, Vietnam in 2021, Cited 95. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

The multicomponent synthesis of 1-amidoalkyl naphthols and polyhydroquinolines has been developed as an atom-economic procedure catalyzed by a deep eutectic solvent ([CholineCl][ZnCl2](3)). The reactions proceed smoothly at low temperatures for a short reaction time without the use of toxic and volatile organic solvents. Deep eutectic solvents are capable of not only allowing multicomponent reactions to proceed in high yield but also controlling the selectivity towards desired products. The mechanistic insight was examined by HRMS (ESI) to propose a plausible mechanism. Furthermore, [CholineCl][ZnCl2](3) can be recycled in up to three consecutive cycles with an insignificant loss of catalytic activity under the optimized conditions.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Nguyen, VT; Nguyen, HT; Tran, PH or concate me.. Application In Synthesis of 4-Methoxybenzaldehyde

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Authors Alqahtani, AM; Bayazeed, AA in ELSEVIER published article about DESIGN; ANTIOXIDANT; INHIBITORS; APOPTOSIS in [Alqahtani, Alaa M.] Umm Al Qura Univ, Coll Pharm, Pharmaceut Chem Dept, Mecca 21955, Saudi Arabia; [Bayazeed, Abrar A.] Umm Al Qura Univ, Coll Appl Sci, Chem Dept, Mecca 21955, Saudi Arabia in 2021, Cited 49. Recommanded Product: 4-Methoxybenzaldehyde. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

Ten new pyridine linked various substituted thiazole hybrids through (hydrazonomethyl) phenoxy-acetamide spacer were synthesized. The synthetic strategy was based on the reaction of the precursor 2-(4-((2-carbamothioylhydrazono)methyl)phenoxy)-N-(pyridin-2-yl)acetamide (3) with various alpha-halogenated carbonyl compounds (namely; phenacyl bromides, ethyl bromoacetate, diethyl bromomalonate and 3-chloropentane-2,4-dione). Moreover, the cytotoxicity properties of the synthesized compounds have been studied against liver carcinoma (HepG2), laryngeal carcinoma (Hep-2), prostate cancer (PC3), breast cancer (MCF-7) and normal fibroblast cells (W138). The pyridine-thiazole compounds 7 and 10 revealed promising anticancer activity against MCF-7 and HepG2 cell lines with IC50 values in the range 5.36-8.76 mu M compared to the activity of 5-fluorouracil. Docking study provided valuable insights for binding sites of the synthesized compounds with Rho-associated protein kinase (ROCK-1). (C) 2020 The Authors. Published by Elsevier B.V. on behalf of King Saud University.

Recommanded Product: 4-Methoxybenzaldehyde. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Alqahtani, AM; Bayazeed, AA or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Polyionic liquid decorated chitosan beads as versatile metal-free catalysts for catalyzing chemical reactions in aqueous media WOS:000661396500015 published article about POT 3-COMPONENT SYNTHESIS; IONIC-LIQUID; GREEN SYNTHESIS; EFFICIENT; ANTIBACTERIAL; NANOPARTICLES; NANOCATALYST; IRRADIATION; DERIVATIVES; REDUCTION in [Koohestani, Fatemeh; Sadjadi, Samahe] Iran Polymer & Petrochem Inst, Fac Petrochem, Gas Convers Dept, POB 14975-112, Tehran, Iran in 2021, Cited 48. SDS of cas: 123-11-5. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

A new strategy is presented for enhancing the catalytic activity of cross-linked chitosan beads. More precisely, chitosan beads were cross linked with glutaraldehyde and then, vinyl functionalized. In the next step, the vinyl-functionalized beads were polymerized with the as-prepared 1-vinyl-3-butylimidazolium bromide to furnish polyionic liquid on beads. The resultant compositewas subsequently utilized as a metal-free catalyst for catalyzing some classic organic transformations, including Knoevenagel condensation reaction and syntheses of tetrahydrobenzo[b]pyrans and pyrano[2,3-d]pyrimidines in aqueous media under mild reaction conditions. It was found that the novel composite could efficiently promote all of the examined reactions to afford the corresponding products in high yields. Moreover, the catalyst exhibited high recyclability for all reactions. The comparative studies also approved that the activity of the composite was superior compared to cross-linked bead and polyionic liquid. (C) 2021 Elsevier B.V. All rights reserved.

SDS of cas: 123-11-5. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Koohestani, F; Sadjadi, S or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Authors Lin, ZR; Zou, J; Li, SF; Zhang, C; Xie, F; Li, B; Ye, DD in AMER CHEMICAL SOC published article about in [Lin, Zirui; Xie, Feng; Li, Bin] Wuyi Univ, Sch Biotechnol & Hlth Sci, Jiangmen 529020, Peoples R China; [Zou, Jie; Li, Shufen; Ye, Dongdong] Wuyi Univ, Sch Text Mat & Engn, Jiangmen 529020, Peoples R China; [Zhang, Chi] Wuyi Univ, Sch Appl Phys & Mat, Jiangmen 529020, Peoples R China in 2021.0, Cited 56.0. Product Details of 123-11-5. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

Imine reduction is one of the most frequently used transformations in organic synthesis. In this work, we developed novel partially carbonized chitin/Ru microspheres (PCRuMs) featuring a tightly assembled nanofiber structure as a highly efficient catalyst of imine hydroboration for the first time. The hydroboration using HBpin as the hydrogen source proceeds under mild conditions (room temperature and a green solvent). The PCRuM catalyst exhibited excellent catalytic activity, chemoselectivity, and recyclability for the hydroboration of imines. Various functional groups including NO2, C N, CO2Me, and C=C bonds were tolerated. Moreover, the PCRuM catalyst can be reused for up to eight runs without noticeably losing activity.

Product Details of 123-11-5. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Lin, ZR; Zou, J; Li, SF; Zhang, C; Xie, F; Li, B; Ye, DD or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Kim, J; Umerani, MJ; Kurakake, R; Qin, HT; Ziller, JW; Gorodetsky, AA; Park, YS in [Kim, Juhwan; Qin, Huiting; Gorodetsky, Alon A.; Park, Young S.] Univ Calif Irvine, Dept Chem & Biomol Engn, Irvine, CA 92697 USA; [Umerani, Mehran J.; Kurakake, Reina; Gorodetsky, Alon A.] Univ Calif Irvine, Dept Mat Sci & Engn, Irvine, CA 92697 USA; [Ziller, Joseph W.; Gorodetsky, Alon A.] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA; [Park, Young S.] Ulsan Natl Inst Sci & Technol UNIST, Dept Chem, 50 UNIST Gil, Ulsan 44919, South Korea published An aza-Diels-Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines in 2021.0, Cited 51.0. HPLC of Formula: C8H8O2. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.

Quinolines and quinoline-containing macromolecules are renowned for their valuable biological activities and excellent materials properties. Herein, we validate a general strategy for the synthesis of chloro-containing quinoline, benzoquinoline and polybenzoquinoline variants via the aza-Diels-Alder reaction. The described findings could be ultimately implemented in other synthetic pathways and may open new opportunities for analogous quinoline-derived materials.

HPLC of Formula: C8H8O2. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Kim, J; Umerani, MJ; Kurakake, R; Qin, HT; Ziller, JW; Gorodetsky, AA; Park, YS or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

I found the field of Chemistry very interesting. Saw the article Oxidation Under Reductive Conditions: From Benzylic Ethers to Acetals with Perfect Atom-Economy by Titanocene(III) Catalysis published in 2021.0. Application In Synthesis of 4-Methoxybenzaldehyde, Reprint Addresses Gansauer, A (corresponding author), Univ Bonn, Kekule Inst Organ Chem & Biochem, Gerhard Domagk Str 1, D-53121 Bonn, Germany.. The CAS is 123-11-5. Through research, I have a further understanding and discovery of 4-Methoxybenzaldehyde

Described here is a titanocene-catalyzed reaction for the synthesis of acetals and hemiaminals from benzylic ethers and benzylic amines, respectively, with pendant epoxides. The reaction proceeds by catalysis in single-electron steps. The oxidative addition comprises an epoxide opening. An H-atom transfer, to generate a benzylic radical, serves as a radical translocation step, and an organometallic oxygen rebound as a reductive elimination. The reaction mechanism was studied by high-level dispersion corrected hybrid functional DFT with implicit solvation. The low-energy conformational space was searched by the efficient CREST program. The stereoselectivity was deduced from the lowest lying benzylic radical structures and their conformations are controlled by hyperconjugative interactions and steric interactions between the titanocene catalyst and the aryl groups of the substrate. An interesting mechanistic aspect is that the oxidation of the benzylic center occurs under reducing conditions.

Application In Synthesis of 4-Methoxybenzaldehyde. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Funk, P; Richrath, RB; Bohle, F; Grimme, S; Gansauer, A or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

HPLC of Formula: C8H8O2. Authors Feng, F; Li, J; Zhang, ZH; Fu, JX; Zhang, YM; Gu, Q in HIGHER EDUCATION PRESS published article about in [Feng, Fan; Li, Jing; Zhang, Zhihui; Fu, Jiaxu; Zhang, Yumin; Gu, Qiang] Jilin Univ, Coll Chem, Changchun 130012, Peoples R China; [Zhang, Yumin; Gu, Qiang] Natl Local Joint Engn Lab In Situ Convers Drillin, Changchun 130021, Peoples R China in 2021, Cited 38. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

An ultrasonic-assisted synthesis of bis-isoxazole derivatives was developed. Eight 3-(6-chloropyridin-3-yl)-5-{[(3-arylisoxazol-5-yl)methoxy]methyl}isoxazoles were synthesized by 1,3-dipolar cycloaddition reaction between substituted isoxazolyl alkyne compounds and 6-chloro-N-hydroxynicotinimidoyl chloride. The structures of the synthesized compounds were confirmed by HRMS, FTIR, H-1 and C-13 NMR spectroscopy. Wherein, the antifungal and antibacterial activities of target compounds were tested. The synthesized compounds 6a and 6h exhibited better antifungal activity in comparison with the standard drug itraconazole. The minimum inhibitory concentrations(MICs) of both compound 6a and compound 6h were both 4 mu g/mL against Candida albicans ATCC 10231.

About 4-Methoxybenzaldehyde, If you have any questions, you can contact Feng, F; Li, J; Zhang, ZH; Fu, JX; Zhang, YM; Gu, Q or concate me.. HPLC of Formula: C8H8O2

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles