Category: 99-61-6

An article Exploring the copper binding ability of Mets7 hCtr-1 protein domain and His7 derivative: An insight in Michael addition catalysis WOS:000580957500001 published article about ARTIFICIAL METALLOENZYMES; ASYMMETRIC HYDROGENATION; PEPTIDES; COMPLEXES; 8-AMINO-5,6,7,8-TETRAHYDROQUINOLINE; KETONES in [Rimoldi, Isabella; Bucci, Raffaella; Feni, Lucia; Facchetti, Giorgio; Pellegrino, Sara] Univ Milan, Dipartimento Sci Farmaceut, Via Venezian 21, I-20133 Milan, Italy; [Santagostini, Laura] Univ Milan, Dipartimento Chim, Milan, Italy in 2021.0, Cited 48.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6. Computed Properties of C7H5NO3

Mets7is a methionine-rich motif present in hCtr-1 transporter that is involved in copper cellular trafficking. Its ability to bind Cu(I) was recently exploited to develop metallopeptide catalysts for Henry condensation. Here, the catalytic activity ofMets7-Cu(I)complex in Michael addition reactions has been evaluated. Furthermore,His7peptide, in which Met residues have been substituted with His ones, was also prepared. This substitution allowedHis7to coordinate Cu (II), with the obtainment of a stable turn conformation as evicted by CD experiments.His7-Cu (II)proved also to be a better catalyst thanMets7-Cu(I)in the addition reaction. In particular, when the substrate was the (E)-1-phenyl-3-(pyridin-2-yl)prop-2-en-1-one, a conversion of 71% and a significative 58% of e.e. was observed.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Authors Samadani, M; Asadi, B; Mohammadpoor-Baltork, I; Mirkhani, V; Tangestaninejad, S; Moghadam, M in ROYAL SOC CHEMISTRY published article about in [Samadani, Marzieh; Asadi, Beheshteh; Mohammadpoor-Baltork, Iraj; Mirkhani, Valiollah; Tangestaninejad, Shahram; Moghadam, Majid] Univ Isfahan, Catalysis Div, Dept Chem, Esfahan 8174673441, Iran in 2021, Cited 52. Recommanded Product: 99-61-6. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

1,1 ‘-(6-(Propyl amino)-1,3,5-triazine-2,4-diyl)bis(pyridinium) hydrogen sulfate immobillized on halloysite nanotubes [(PATDBP)(HSO4)(2)@HNT] as a solid acid nanocatalyst was successfully synthesized and characterized by various analysis techniques such as FT-IR, TGA, SEM/EDX, elemental mapping, TEM and elemental analysis. This catalyst was found to be highly efficient for the convenient synthesis of naphthopyranopyrimidine derivatives through a one-pot three-component reaction of beta-naphthol, aldehydes and N,N-dimethylbarbituric acid in excellent yields under solvent-free conditions. Furthermore, the catalyst could be recovered and reused five times without any notable loss of its activity.

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Thiomorpholine – Wikipedia,
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An article Diastereoselective synthesis of highly substituted tetrahydroquinolines using benzoylacetonitrile via aza Diels-Alder reaction WOS:000650994000012 published article about STEREOSELECTIVE-SYNTHESIS; QUINOLINE DERIVATIVES; ASYMMETRIC-SYNTHESIS; CASCADE REACTIONS; POVAROV REACTION; CYCLIZATION; CHEMISTRY; FURANS; ACID in [Chen, Chinpiao] Tzu Chi Univ Sci & Technol, Dept Nursing, Hualien 970302, Taiwan; [Palanimuthu, Arunan; Chen, Chinpiao] Natl Dong Hwa Univ, Dept Chem, Hualien 974301, Taiwan; [Lee, Gene-Hsian] Natl Taiwan Univ, Coll Sci, Instrumentat Ctr, Taipei 10617, Taiwan in 2021.0, Cited 61.0. HPLC of Formula: C7H5NO3. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

Diastereoselective aza-Diels-Alder reaction between in situ generated 2-aminophenyl-substituted enones and alpha-cyano-alpha,beta-unsaturated aromatic ketone has been developed. In the presence of TEA as a catalyst prepared highly substituted tetrahydroquinolines with an all-carbon quaternary center in an in situ fashion. Both tetrahydroquinoline isomers (exo and endo) with excellent diastereoselectivity and high yields were synthesized in very mild conditions. (C) 2021 Published by Elsevier Ltd.

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Thiomorpholine – Wikipedia,
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I found the field of Chemistry very interesting. Saw the article Knoevenagel condensation in aqueous media promoted by 2,2 ‘-bipyridinium dihydrogen phosphate as a green efficient catalyst published in 2021.0. Recommanded Product: 3-Nitrobenzaldehyde, Reprint Addresses Shirini, F (corresponding author), Univ Guilan, Coll Sci, Dept Chem, Univ Campus 2, Rasht 4133519141, Iran.. The CAS is 99-61-6. Through research, I have a further understanding and discovery of 3-Nitrobenzaldehyde

A 2,2 ‘-Bipyridine-based ionic compound named 2,2 ‘-bipyridinium dihydrogen phosphate was synthesized by addition of phosphoric acid to a solution of 2,2 ‘-Bipyridine in dichloromethane. After the characterization using FT-IR, mass, H-1, C-13 and P-31 NMR techniques, it was used as a Bronsted dicationic acidic catalyst for the promotion of the synthesis of 2-arylidene malononitrile and 5-arylidene barbituric acid derivatives via Knoevenagel condensation reaction in water. Some of the advantages of this method are the utilization of an easy preparable, cost-effective and eco-friendly organic salt as a catalyst within high rates and yields of the reactions, simple and quick work-up and acceptable reusability of the catalyst.

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Thiomorpholine – Wikipedia,
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Quality Control of 3-Nitrobenzaldehyde. In 2021 LETT ORG CHEM published article about PRIMARY ALCOHOLS; TERMINAL ALKYNES; NANOPARTICLES; AMINE; WATER; GAS in [Yu, Min] Nanjing Xiaozhuang Univ, Sch Environm Sci, Nanjing 211171, Peoples R China; [Yu, Min; Wu, Chaolong; Zhou, Li; Yao, Xiaoquan] Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Technol, Nanjing 210016, Peoples R China; [Zhu, Li] Nanjing Med Univ, Sch Pharm, Nanjing 210029, Peoples R China in 2021, Cited 59. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6.

The oxidation of aldehydes is an efficient methodology for the synthesis of carboxylic acids. Herein we hope to report a simple, efficient and recyclable protocol for aerobic oxidation of aldehydes to carboxylic acid by using C3N4 supported silver nanoparticles (Ag/C3N4) as a catalyst in aqueous solution under mild conditions. Under standard conditions, the corresponding carboxylic acids can be obtained in good to excellent yields. In addition, Ag/C3N4 is convenient for recovery and could be reused three times with satisfactory yields.

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Thiomorpholine – Wikipedia,
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Recommanded Product: 3-Nitrobenzaldehyde. In 2021 J IRAN CHEM SOC published article about SELECTIVE SYNTHESIS; ANTITUMOR-ACTIVITY; DERIVATIVES; CATALYST; SILICA; SYSTEM; ROUTE; WATER in [Gulati, Susheel; Singh, Rajvir; Sangwan, Suman; Rana, Suprita] Chaudhary Charan Singh Haryana Agr Univ, Dept Chem, Hisar 125004, Haryana, India in 2021, Cited 29. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6.

An efficient and facile synthesis of substituted novel benzimidazoles (3a-3h) mediated by fruit juices viz.Cocos nuciferaL. juice,Citrus limettajuice andCitrus sinensisL. juice, via condensation of substituted aldehydes (1a-1h) ando-phenylenediammine (2a) under solvent-free condition at room temperature is presented in this paper. The purity of compounds was confirmed by melting point and thin layer chromatography. All synthesized compounds (3a-3h) were fully characterized via NMR and FTIR spectral data and evaluated for in vitro herbicidal activity againstRaphanus sativusL. (Radish) seeds. The compounds (3a-3h) were also evaluated for their antibacterial activity againstErwinia cartovoraandXanthomonas citriby inhibition zone method. Antifungal activity was also determined againstRhizoctonia solaniandColletotrichum gloeosporioidesby poisoned food techniques method. From activity data, it was found that compounds3dand3ewere most active againstR.sativusL. (root) andR.sativusL. (shoot), respectively. Compound3ghas shown maximum inhibition zone i.e. 8.00 mm againstE.cartovoraat 2000 mu g/mL concentration. MaximumX.citriigrowth was inhibited by compounds3ashowing inhibition zone 5.20 mm at highest concentration. Compound3fwas found most active againstR.solani and C.gloeosporioidesfungus at 2000 mu g/mL concentration. In comparison with the conventional methods, the present method complies with several key requirements of green chemistry principles such as the utilization of renewable feedstock, auxiliary aqueous conditions and reduces waste with the use of nature-derived catalyst. Therefore, the present method offers an attractive option because of its ecological safety, environmental acceptance, cost effective and easy workup process. [GRAPHICS] .

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Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Formula: C7H5NO3. Authors Dutta, A; Rohman, MA; Nongrum, R; Thongni, A; Mitra, S; Nongkhlaw, R in ROYAL SOC CHEMISTRY published article about in [Dutta, Arup; Rohman, Mostofa A.; Thongni, Aiborlang; Mitra, Sivaprasad; Nongkhlaw, Rishanlang] North Eastern Hill Univ, Dept Chem, Ctr Adv Studies Chem, Shillong 793022, Meghalaya, India; [Nongrum, Ridaphun] Sankardev Coll, Shillong, Meghalaya, India in 2021.0, Cited 41.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

Herein, we report an intramolecular radical cyclization reaction towards the synthesis of pyrrolidinone derivatives via metal-free photoredox catalysis under irradiation from blue LEDs. Some of the remarkable features of this protocol include synthetic efficiency, green reaction profile, easy isolation of products and short reaction time. The photophysical properties of synthesized compounds were investigated via steady state and time-resolved fluorescence spectroscopy in the solid state. Results showed the promising opportunity for their spectral tuning together with large Stokes-shifted and highly active fluorescence emission, thus indicating that these molecular scaffolds can be effective probes for the biological applications and development of opto-electronic devices.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Quality Control of 3-Nitrobenzaldehyde. In 2021 LETT ORG CHEM published article about DERIVATIVES in [Suryawanshi, Vikas B.] KMC Coll, Dept Chem, Khopoli 410203, Maharashtra, India; [Suryawanshi, Vikas B.] Mumbai Univ, Mumbai, Maharashtra, India; [Momin, Kalimoddin, I] Rajarshi Shahu Coll, Dept Chem, Latur 413512, Maharashtra, India; [Momin, Kalimoddin, I; Dawle, Jairaj K.] SRTM Univ, Nanded, India; [Dawle, Jairaj K.] Maharashtra Mahavidyalaya, Res Lab Pure & Appl Chem, Nilanga 413521, India; [Mathapati, Sushil R.] Shri Madhavrao Patil Mahavidyalaya, Dept Chem, Murum 413605, India; [Mathapati, Sushil R.] Dr BAM Univ, Aurangabad, Maharashtra, India in 2021, Cited 31. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6.

Solvent free synthesis of dihydropyrano[3,2-b]chromenediones was formulated via multicomponent reactions of kojic acid, dimedone and several substituted aromatic aldehydes catalyzed with BCl3. Reactions progressed efficiently and the corresponding heterocyclic products were obtained in good to high yields within short period. The developed protocol is one of the better and efficient alternative methods for the synthesis of dihydropyrano[3,2-b]chromenediones. The simple reaction procedure, easy separation of products, radially available catalyst are certain benefits of this reported protocol.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

HPLC of Formula: C7H5NO3. Authors Olyaei, A; Adl, A; Vessally, E in SPRINGER published article about in [Olyaei, Abolfazl; Adl, Alireza; Vessally, Esmail] Payame Noor Univ PNU, Dept Chem, PO BOX, Tehran 193954697, Iran in 2021.0, Cited 30.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

An efficient and convenient procedure for the synthesis of novel 6-hydroxy-14aryl-8H-dibenzo[a,i]xanthene-8,13(14-H)-dione derivatives has been developed by one-pot, three-component condensation reaction between 2-hydroxynaphthalene-1,4-dione, aromatic aldehydes and 2,3-naphthalenediol in glacial acetic acid under reflux conditions. This domino reaction implies Knoevenagel condensation, Michael addition, intramolecular cyclization and dehydration. The reaction avoids tedious workup procedure due to the direct precipitation of products from the reaction medium. The notable features of this domino transformation are operational simplicity, clean reaction, easy handling, easy purification process and high yields of the products.

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Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Authors Zaiter, J; Hibot, A; Hafid, A; Khouili, M; Neves, CMB; Simoes, MMQ; Neves, MGPMS; Faustino, MAF; Dagci, T; Saso, L; Armagan, G in ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER published article about in [Zaiter, Jamila; Hibot, Achraf; Hafid, Abderrafia; Khouili, Mostafa] Univ Sultan Moulay Slimane, Fac Sci & Tech, Lab Chim Organ & Analyt, BP 523, Beni Mellal 23000, Morocco; [Neves, Claudia M. B.; Simoes, Mario M. Q.; Neves, M. Graca P. M. S.; Faustino, M. Amparo F.] Univ Aveiro, Dept Chem, LAQV REQUIMTE, P-3810193 Aveiro, Portugal; [Dagci, Taner] Ege Univ, Fac Med, Dept Physiol, TR-35100 Izmir, Turkey; [Saso, Luciano] Sapienza Univ Rome, Dept Physiol & Pharmacol Vittorio Erspamer, Ple Aldo Moro 5, I-00185 Rome, Italy; [Armagan, Guliz] Ege Univ, Fac Pharm, Dept Biochem, TR-35100 Izmir, Turkey in 2021, Cited 33. Application In Synthesis of 3-Nitrobenzaldehyde. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

The loss of neurons is strongly correlated with aging and aging-associated disorders. In this study, cell viability assays and mitochondrial function were performed to evaluate the effect of new spiro-pyrazole derivatives, prepared from aldehydes and 3-amino-1-phenyl-2-pyrazolin-5-one, on neuroprotection in an in vitro model of dopaminergic cell death induced by 1-methyl-4-phenylpyridinium (MPP+). The percentages of neuroprotection by derivatives were found between 21.26% and 52.67% at selected concentrations (10-50 mu M) with compound 4d exerting the best neuroprotective effect. The results show that the studied spiropyrazolones perform important roles in dopaminergic neuroprotection and can be used for potential new therapies in the treatment of neurodegenerative disorders including Parkinson’s disease. (C) 2020 Elsevier Masson SAS. All rights reserved.

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Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem