Category: 99-61-6

An article Simple practical method for synthesis of trisubstituted imidazoles: an efficient copper catalyzed multicomponent reaction WOS:000667711300005 published article about LACTIM-LACTAM TAUTOMERISM; PHOTOPHYSICAL PROPERTIES; SUBSTITUTED IMIDAZOLES; SPECTROSCOPIC APPROACH; ANTIFUNGAL AGENTS; IONIC LIQUIDS; GREEN; OXIDATION; HYDROGEN; SYSTEM in [Kadu, Vikas D.; Mali, Ganesh A.; Khadul, Siddheshwar P.; Kothe, Gokul J.] Punyashlok Ahilyadevi Holkar Solapur Univ, Sch Chem Sci, Solapur 413255, Maharashtra, India in 2021.0, Cited 59.0. Category: thiomorpholine. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

A rapid practical process has been developed for synthesis of 2,4,5-trisubstituted-imidazoles in excellent yields up to 95% from readily available starting materials. In this CuI catalyzed synthesis, trisubstituted imidazoles were afforded in short reaction times, wherein the substrate scope is well explored with benzoin as well as benzil reacting with different aldehydes in the presence of ammonium acetate as the nitrogen source.

Category: thiomorpholine. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Kadu, VD; Mali, GA; Khadul, SP; Kothe, GJ or concate me.

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

Authors Kargar, S; Elhamifar, D; Zarnegaryan, A in ELSEVIER published article about in [Kargar, Shiva; Elhamifar, Dawood; Zarnegaryan, Ali] Univ Yasuj, Dept Chem, Yasuj 7591874831, Iran in 2021, Cited 83. SDS of cas: 99-61-6. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

A novel ionic liquid modified graphene oxide supported Mo-complex [GO@IL/MoO2(acae)(2)] was successfully prepared, characterized and its catalytic application was investigated. The GO@IL/MoO2(acae)(2) catalyst was prepared through the surface modification of graphene oxide with alkyl imidazolium chloride followed by treatment with molybdenyl acetylacetonate. The GO@IL/MoO2(acae)(2) catalyst was characterized by using FT-IR, PXRD, TGA, EDX, and SEM analyses. This catalyst showed high activity in the green production of pyrazolo[b] phthalazine dione derivatives under ultrasonic conditions. The designed catalyst was effectively recovered and successfully reused at least eight times without significant loss in its efficiency.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

I found the field of Biochemistry & Molecular Biology; Chemistry; Pharmacology & Pharmacy very interesting. Saw the article Dihydroquinoline derivative as a potential anticancer agent: synthesis, crystal structure, and molecular modeling studies published in 2021.0. Name: 3-Nitrobenzaldehyde, Reprint Addresses Vaz, WF (corresponding author), Univ Estadual Goias, BR-75132400 Anapolis, Go, Brazil.; Vaz, WF (corresponding author), Inst Fed Educ Ciencia & Tecnol Mato Grosso, BR-78455000 Lucas Do Rio Verde, MT, Brazil.. The CAS is 99-61-6. Through research, I have a further understanding and discovery of 3-Nitrobenzaldehyde

Cancer is one of the leading causes of death worldwide and requires intense and growing research investments from the public and private sectors. This is expected to lead to the development of new medicines. A determining factor in this process is the structural understanding of molecules with potential anticancer properties. Since the major compounds used in cancer therapies fail to encompass every spectrum of this disease, there is a clear need to research new molecules for this purpose. As it follows, we have studied the class of quinolinones that seem effective for such therapy. This paper describes the structural elucidation of a novel dihydroquinoline by single-crystal X-ray diffraction and spectroscopy characterization. Topology studies were carried through Hirshfeld surfaces analysis and molecular electrostatic potential map; electronic stability was evaluated from the calculated energy of frontier molecular orbitals. Additionally, in silico studies by molecular docking indicated that this dihydroquinoline could act as an anticancer agent due to their higher binding affinity with human aldehyde dehydrogenase 1A1 (ALDH 1A1). Tests in vitro were performed for VERO (normal human skin keratinocytes), B16F10 (mouse melanoma), and MDA-MB-231 (metastatic breast adenocarcinoma), and the results certified that compound as a potential anticancer agent. [GRAPHICS] .

Name: 3-Nitrobenzaldehyde. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Vaz, WF; Custodio, JMF; D’Oliveira, GDC; Neves, BJ; Junior, PSC; Filho, JTM; Andrade, CH; Perez, CN; Silveira-Lacerda, EP; Napolitano, HB or concate me.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Computed Properties of C7H5NO3. Authors Al-Adhami, HJ; Al-Majidi, SMH in MAIK NAUKA/INTERPERIODICA/SPRINGER published article about in [Al-Adhami, H. J.; Al-Majidi, S. M. H.] Univ Baghdad, Coll Sci, Dept Chem, Baghdad 10071, Iraq in 2021.0, Cited 26.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

The condensation of 6-amino-1,3-dimethyluracil with substituted benzaldehydes gave six Schiff base derivatives which were brought into cyclizations with sodium azide, anthranilic acid, and 2-sulfanylbenzoic acid to afford new dihydrotetrazoles, dihydroquinazolin-4-ones, and 1,3-benzothiazine-4-ones containing a 1,3-di-methyluracil fragment. The structure of the newly synthesized compounds was confirmed by FTIR and NMR spectroscopy, and their in vitro antioxidant and antimicrobial activities against some bacterial and fungal strains were evaluated.

Computed Properties of C7H5NO3. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Al-Adhami, HJ; Al-Majidi, SMH or concate me.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Zhan, SC; Fang, RJ; Sun, J; Yan, CG in [Zhan, Shao-Cong; Fang, Ren-Jie; Sun, Jing; Yan, Chao-Guo] Yangzhou Univ, Coll Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China published Diastereoselective synthesis of spiro[carbazole-3,5 ‘-pyrimidines] and spiro[carbazole-3,1 ‘-cyclohexanes] via four-component reaction in 2021.0, Cited 55.0. Name: 3-Nitrobenzaldehyde. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6.

Functionalized spiro[carbazole-3,5 ‘-pyrimidines] and spiro[carbazole-3,1 ‘-cyclohexanes] were efficiently synthesized in satisfactory yields with high diastereoselectivity by CuSO4 catalyzed multicomponent reaction of indole-2-acetate, aromatic aldehyde and 1,3-dimethylbarbituric acid or dimedone. The reaction was finished with sequential Diels-Alder reaction of both in situ generated indole-2,3-quinodimethane and a dienophile. Additionally, the initially formed spiro[carbazole-3,5 ‘-pyrimidines] were converted to dehydrogenated spiro[carbazole-3,5 ‘-pyrimidines] by DDQ oxidation. The initially formed spiro[carbazole-3,1 ‘-cyclohexanes] were converted to delta-valerolactone-substituted carbazoles by a DDQ promoted Baeyer-Villiger oxidation process.

Name: 3-Nitrobenzaldehyde. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Zhan, SC; Fang, RJ; Sun, J; Yan, CG or concate me.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Synthesis of pyrano[2,3-d]pyrimidines and pyrido[2,3-d]pyrimidines in the magnetized deionized water based on UV-visible study WOS:000577578900002 published article about ONE-POT SYNTHESIS; CATALYST-FREE; 3-COMPONENT SYNTHESIS; DERIVATIVES; EFFICIENT; GREEN; COMPLEXITY; PYRIDO in [Bakherad, Mohammad; Bagherian, Ghadamali; Rezaeifard, Amin; Mosayebi, Fatemeh; Shokoohi, Behzad; Keivanloo, Ali] Shahrood Univ Technol, Fac Chem, Shahrood 3619995161, Iran in 2021, Cited 43. Recommanded Product: 99-61-6. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

A green synthetic route to the facile one-pot multicomponent synthesis of pyrano[2,3-d]pyrimidines and pyrido[2,3-d]pyrimidines have been developed using magnetized deionized water (MDW) as a green solvent under catalyst-free conditions. All reactions carried out in a short period of time and the products are obtained in high-to-excellent yields. The developed synthetic technique offers numerous advantages including eco-friendly, clean synthesis, simplicity, low cost, short reaction times, high reaction yields, and easy workup compared to the traditional synthetic method. Moreover, the reaction rates were followed spectrophotometrically by monitoring the changes in the absorption spectrum of the reaction mixture in ordinary deionized water and MDW.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Domino Processes of Arynes Reacting with Three Classes of Nucleophiles for Organic Syntheses WOS:000604339500001 published article about CARBONYL-COMPOUNDS; ASYMMETRIC-SYNTHESIS; EPOXIDATION; MILD; BENZYNE; 1,2-DIHYDROQUINOLINES; DERIVATIVES; ALDEHYDES; EPOXIDES; ACCESS in [Hwu, Jih Ru; Panja, Avijit; Gupta, Nitesh K.; Tan, Kui-Thong; Lin, Chun-Cheng; Hwang, Kuo-Chu; Huang, Wen-Chieh; Tsay, Shwu-Chen] Natl Tsing Hua Univ, Dept Chem, Hsinchu 30013, Taiwan; [Hwu, Jih Ru; Panja, Avijit; Gupta, Nitesh K.; Tan, Kui-Thong; Lin, Chun-Cheng; Hwang, Kuo-Chu; Huang, Wen-Chieh; Tsay, Shwu-Chen] Natl Tsing Hua Univ, Frontier Res Ctr Fundamental & Appl Sci Matters, Hsinchu 30013, Taiwan; [Hu, Yu-Chen] Natl Tsing Hua Univ, Dept Chem Engn, Hsinchu 30013, Taiwan; [Hsu, Ming-Hua] Natl Changhua Univ Educ, Dept Chem, Changhua 50007, Changhua, Taiwan in 2021.0, Cited 60.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6. COA of Formula: C7H5NO3

Synthetic application of arynes is broadened by their reactions with neutral N-, S-, and O-containing nucleophiles to produce three types of compounds. Accordingly, 1,2-dihydroquinolines are synthesized from Schiff bases, alkynes, and arynes through a Diels-Alder reaction. Epoxides are prepared from thioethers and arynes along with aldehydes or ketones through a Johnson-Corey-Chaykovsky reaction. Phenolic ethers are produced from allyl ethers and arynes through a Claisen-type rearrangement. These target molecules, including natural products gamma-asarone, asaricin, and a cholesteryl phenolic ether, are formed through reactions initiated by arynes. These new reactions share a prevailing feature of domino processes, which are carried out in a single flask and afford the desired products in good to high yields.

About 3-Nitrobenzaldehyde, If you have any questions, you can contact Hwu, JR; Panja, A; Gupta, NK; Hu, YC; Tan, KT; Lin, CC; Hwang, KC; Hsu, MH; Huang, WC; Tsay, SC or concate me.. COA of Formula: C7H5NO3

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Product Details of 99-61-6. Recently I am researching about PYRAZOLE DERIVATIVES; HETEROGENEOUS CATALYST; SILICA NANOPARTICLES; EFFICIENT CATALYST; CONTROLLED-RELEASE; ONE-POT; GREEN; NANOCATALYST; COMPOSITE; ACID, Saw an article supported by the University of Kashan. Published in WILEY in HOBOKEN ,Authors: Mirheidari, M; Safaei-Ghomi, J. The CAS is 99-61-6. Through research, I have a further understanding and discovery of 3-Nitrobenzaldehyde

A core-shell structured magnetic metal-mesoporous microsphere materials NiFe2O4@SiO2@Al-MS in which magnetic particles of NiFe2O4 are core and ordered mesoporous silica are shell, incorporated with aluminum to modify acid-catalyzed reactions. The catalyst was synthesized by Pluronic P123 as a first surfactant and a small quantity of cetrimonium bromide as a template for assistant in acidic medium to create a porous layer. The structural characterization of the catalyst was assessed by Fourier transform infrared (FT-IR), scanning electron microscopy (SEM), X-ray diffraction (XRD), energy-dispersive X-ray (EDX), vibrating-sample magnetometer (VSM), and Brunauer-Emmett-Teller (BET) analyses. The catalyst demonstrated considerable magnetic properties, a unique mesoporous structure with great surface area (370.36 m(2) g(-1)), high-value recovery, and reusability. The catalyst performance was evaluated for the synthesis of indenopyrazolones via the condensation of ninhydrin, phenylhydrazine, and various aldehydes. The mild conditions for the synthesis, easy workup, and short reaction time are the considerable benefits of the reaction in the presence of Nife(2)O(4)@SiO2@Al-MS as a catalyst.

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

In 2021 J ORG CHEM published article about DIELS-ALDER REACTION; ENANTIOSELECTIVE CONSTRUCTION; SUBSTITUTED CARBAZOLES; ASYMMETRIC-SYNTHESIS; EFFICIENT SYNTHESIS; 4+2 CYCLOADDITION; RELAY CATALYSIS; RAPID ACCESS; DERIVATIVES; TETRAHYDROCARBAZOLES in [Zhan, Shao-Cong; Fang, Ren-Jie; Sun, Jing; Yan, Chao-Guo] Yangzhou Univ, Coll Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China in 2021, Cited 96. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6. Safety of 3-Nitrobenzaldehyde

In the presence of copper sulfate, the three-component reaction of aromatic aldehydes, ethylindole-3-acetate and 4-arylidene-5-methyl-2-phenylpyrazol-3-ones, in refluxing toluene afforded spiro[carbazole-3,4′-pyrazoles] in good yields with high diastereoselectivity. More importantly, the similar CuSO4 promoted the four-component reaction of two molecular aromatic aldehydes with ethylindole-3-acetate and 5-methyl-2-phenyl-pyrazol-3-one resulted in 2,4-diarylspiro[carbazole-3,4′-pyrazoles] in satisfactory yields. Additionally, CuSO4 promoted the four-component reaction of two molecular aromatic aldehydes, ethylindole-3-acetate and 2-phenylthiazol-4-one, in refluxing toluene gave 2,4-diarylspiro[carbazole-3,4′-thiazoles] with diastereomeric ratios in the range of 3:1 to 20:1.

Safety of 3-Nitrobenzaldehyde. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Zhan, SC; Fang, RJ; Sun, J; Yan, CG or concate me.

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

Product Details of 99-61-6. Authors Jafari-Chermahini, MT; Tavakol, H in WILEY-V C H VERLAG GMBH published article about in [Jafari-Chermahini, Mohammad T.; Tavakol, Hossein] Isfahan Univ Technol, Dept Chem, Esfahan 8415683111, Iran in 2021, Cited 40. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

Various spinel iron oxide nanoparticles (MFe(2)O4, M: Ca, Co, Cu, Fe, Hg, Mg, Mn, Ni, Sn and Zn) have been prepared using a single step coprecipitation method. Nanoparticles were characterized using XRD, FESEM, FT-IR and UV-Vis diffuse-reflectance spectroscopy. The catalytic activities of the synthesized nanoparticles in Hantzsch reaction have been studied. HgFe2O4 NPs exhibits the highest catalytic activity than others. The structural properties of synthesized 1,4-dihydropyridine were characterized by mass spectrometry, FT-IR and H-1- and C-13-NMR. Finally, the in silico molecular simulations for screening of blocking ability of synthesized 1,4-dihydropyridine against various TRPV6 proteins were performed. These studies revealed that examined 1,4-dihydropyridines are promising TRPV6 calcium channel blockers. As a result, molecular modeling confirmed that synthesized 1,4-DHPs are docked on the pore region of the examined TRPV6 channels.

Product Details of 99-61-6. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Jafari-Chermahini, MT; Tavakol, H or concate me.

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