Some scientific research about 3-Nitrobenzaldehyde

Welcome to talk about 99-61-6, If you have any questions, you can contact Gupta, R; Arora, G; Yadav, P; Dixit, R; Srivastava, A; Sharma, RK or send Email.. Name: 3-Nitrobenzaldehyde

Authors Gupta, R; Arora, G; Yadav, P; Dixit, R; Srivastava, A; Sharma, RK in ROYAL SOC CHEMISTRY published article about CATALYZED OXIDATIVE SYNTHESIS; ONE-POT SYNTHESIS; 4(3H)-QUINAZOLINONE DERIVATIVES; CASCADE SYNTHESIS; BENZYL ALCOHOLS; QUINAZOLINONES; METAL; EFFICIENT; SILICA; OXIDE in [Gupta, Radhika; Arora, Gunjan; Yadav, Priya; Dixit, Ranjana; Sharma, Rakesh Kumar] Univ Delhi, Green Chem Network Ctr, Dept Chem, Delhi 110007, India; [Yadav, Priya; Srivastava, Anju] Univ Delhi, Hindu Coll, Dept Chem, Delhi 110007, India in 2021, Cited 74. Name: 3-Nitrobenzaldehyde. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

In the present work, we report the design and fabrication of a copper-containing ionic liquid supported magnetic nanocatalyst via a convenient and straightforward synthetic approach for the formation of 2-phenylquinazolin-4(3H)-ones using o-aminobenzamide and benzaldehydes as the reaction partners. The successful formation and properties of the as-prepared catalyst have been thoroughly investigated using diverse physico-chemical techniques including FT-IR, XRD, FE-SEM, TEM, ICP, VSM, BET and TGA. Using this nanocatalytic system, a variety of 2-phenylquinazolin-4(3H)-ones are synthesized in excellent yields with operational ease and short reaction times in an environmentally preferable solvent under open air and without using any external oxidizing agent. Besides, the catalyst possessed facile magnetic recoverability and remarkable reusability for six consecutive runs without any appreciable decrease in the catalytic efficiency.

Welcome to talk about 99-61-6, If you have any questions, you can contact Gupta, R; Arora, G; Yadav, P; Dixit, R; Srivastava, A; Sharma, RK or send Email.. Name: 3-Nitrobenzaldehyde

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Application In Synthesis of 3-Nitrobenzaldehyde. Bye, fridends, I hope you can learn more about C7H5NO3, If you have any questions, you can browse other blog as well. See you lster.

Authors Wu, ZH; He, ZC; Xu, YK; Wang, J; Lu, XH; Xia, QH; Zhou, D in SPRINGER published article about in [Wu, Zhonghan; He, Zhechao; Xu, Yinke; Wang, Jing; Lu, Xinhuan; Xia, Qinghua; Zhou, Dan] Hubei Univ, Minist Of Educ, Key Lab Synth & Applicat Organ Funct Mol, Wuhan 430062, Peoples R China in 2021.0, Cited 21.0. Application In Synthesis of 3-Nitrobenzaldehyde. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

From the view of energy saving and environment protection, green catalysis has become one of the most important goals of chemists, including both the green preparation of catalyst and the highly efficient catalysis under mild reaction condition. Herein, N,N-dimethylaminopropyl-functionalized hybrid zeolite is firstly synthesized by one-step non-templating method, which is characterized by powder X-ray diffraction, Fourier-transform IR, thermogravimetric analysis, element analysis, scanning electron microscope, water contact angle measurements, inductively coupled plasma atomic emission spectrometry, and N-2 adsorption-desorption measurements. The functionalized hybrid zeolite can be directly used as base catalyst without any post modification and achieve high yields of corresponding products in the Knoevenagel condensation of benzaldehyde (or substituted benzaldehyde) with ethyl cyanoacetate at room temperature by using ethanol as solvent. By the comparison with other zeolite catalysts, the unique and excellent catalytic properties of N,N-dimethylaminopropyl-functionalized hybrid zeolite was ascribed to not only the synergic effect of basic property and hydrophobic/lipophilicity of the organic groups, but also the easier accessibility of bulky substrate molecules with highly exposed catalytic active sites over the solid catalyst. The recycling and control experiments show that it owes excellent reusable stability.

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Safety of 3-Nitrobenzaldehyde. In 2021 APPL ORGANOMET CHEM published article about HYDROXYAPATITE-CORE-SHELL-GAMMA-FE2O3 NANOPARTICLES; 5-SUBSTITUTED 1H-TETRAZOLES; MAGNETIC NANOPARTICLES; HETEROGENEOUS CATALYST; RECYCLABLE CATALYST; HIGHLY EFFICIENT; FACILE SYNTHESIS; DERIVATIVES in [Sorkhabi, Serve; Mozafari, Roya; Ghadermazi, Mohammad] Univ Kurdistan, Fac Sci, Dept Chem, Sanandaj, Iran in 2021, Cited 77. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6.

In the current research, much attention is paid to heterogenized nanostructure. Herein, we report the green synthesis magnetic nanoparticles (MNPs) of cobalt ferrite by the immobilization of erbium (Er) coated with folic acid (FA) which show effective catalytic properties and recyclability. Full characterizations with field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), X-ray atomic mapping, thermal gravimetric analysis (TGA), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), inductively coupled plasma-optical emission spectrometry (ICP-OES), and Fourier-transform infrared (FT-IR) spectroscopy techniques were undertaken to uncover structural properties of the prepared magnetic catalyst. The obtained nanohybrid complexes as efficient, recyclable, and green heterogeneous systems pave the way for producing pyrano[2,3-d]pyrimidinone and dihydropyrano[3,2-c]chromenes derivatives by the one-pot three-component condensation reaction of various aldehydes, malononitrile, and hydroxycoumarin or barbituric acid in green condition. This easily prepared organometalic catalyst presents many superiorities such as operational simplicity, high yield, short reaction time, utilization of commercially available or easily accessible starting materials, eco-friendly properties, and excellent purity. Most importantly, erbium-FA-coated CoFe2O4 can be easily separated and recycled from the reaction system using an external magnetic field. The magnetically recoverable biocatalyst can be recycled and reused six times while maintaining high activities. The activity of the magnetic catalyst can be maintained at more than 80% of that of the previous cycle. This research solves the recovery problem encountered in industrial applications of biocatalysts and presents a clean and green method for preparing pyrimidinones and chromenes.

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An article Synthesis and Characterization of Pine-cone Derived Carbon-based Solid Acid: a Green and Recoverable Catalyst for the Synthesis of Pyrano_pyrazole, Amino-benzochromene, Amidoalkyl Naphthol and Thiazolidinedione Derivatives WOS:000631152000009 published article about IN-VITRO; BIOLOGICAL EVALUATION; EFFICIENT SYNTHESIS; REUSABLE CATALYST; ONE-POT; CELLULOSE; DESIGN; ADSORPTION; COMPOSITE; BEARING in [Ghorbani, Fatemeh; Pourmousavi, Seied Ali; Kiyani, Hamzeh] Damghan Univ, Sch Chem, Damghan 36715364, Iran; [Pourmousavi, Seied Ali] Damghan Univ, Inst Biol Sci, Damghan 3671641167, Iran in 2021, Cited 66. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6. Formula: C7H5NO3

In this report, SO3H-functionalized Carbon nanoparticles (Pine-SO3H) with high acid density have been synthesized by the thermal treatment of sulfuric acid with Pine-Cone as carbon-based at 180 degrees C in a sealed autoclave in a one-step procedure. The resulted Nanocatalyst was characterized by FT-IR, TGA, XRD, FE-SEM and elemental analysis (EA). The result of characterization was shown that the carbon-based acid is amorphous with polycyclic aromatic carbon sheets attached plentiful -OH, -COOH, and -SO3H groups. The catalytic activities of Pine-SO3H was investigated in the highly efficient synthesis of pyrano[2,3-c] pyrazole, amino-benzochromenes, amidoalkyl naphthol and 5-arylidene-2,4-thiazolidinedione derivatives. The application of Pine-SO3H in the synthesis offers several advantages such as simple procedure with an easy work-up, recoverable catalyst, mild condition, eco-friendliness, excellent yields, short reaction times and use of an inexpensive catalyst.

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Product Details of 99-61-6. Welcome to talk about 99-61-6, If you have any questions, you can contact Kamali, F; Shirini, F or send Email.

Product Details of 99-61-6. Authors Kamali, F; Shirini, F in TAYLOR & FRANCIS LTD published article about in [Kamali, Fatemeh; Shirini, Farhad] Univ Guilan, Dept Chem, Coll Sci, Rasht 41335, Iran in 2021.0, Cited 75.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

Melamine, as an inexpensive and commercially available reagent, can be efficiently used for the promotion of the synthesis of 3,3 ‘-(4-arylmethylene) bis-(4-hydroxycoumarins), 2,2 ‘-arylmethylene bis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-ones) and 2-amino-4H-chromene derivatives. In addition to the mild conditions, this method provides other important advantages including simple work-up procedure, environmental friendliness, short reaction times, high yields of the products and use of a cheap, stable and reusable catalyst.

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Product Details of 99-61-6. Welcome to talk about 99-61-6, If you have any questions, you can contact Babaee, S; Chehardoli, G; Akbarzadeh, T; Zolfigol, MA; Mahdavi, M; Rastegari, A; Moghadam, FH; Najafi, Z or send Email.

Authors Babaee, S; Chehardoli, G; Akbarzadeh, T; Zolfigol, MA; Mahdavi, M; Rastegari, A; Moghadam, FH; Najafi, Z in WILEY-V C H VERLAG GMBH published article about in [Babaee, Saeed; Zolfigol, Mohammad Ali] Bu Ali Sina Univ, Fac Chem, Dept Organ Chem, Hamadan 6517838683, Hamadan, Iran; [Chehardoli, Gholamabbas; Najafi, Zahra] Hamadan Univ Med Sci, Sch Pharm, Dept Med Chem, Hamadan 6517838678, Iran; [Akbarzadeh, Tahmineh; Rastegari, Arezoo] Univ Tehran Med Sci, Fac Pharm, Dept Med Chem, Tehran 1417614411, Iran; [Mahdavi, Mohammad] ACECR, Royan Inst Biotechnol, Cell Sci Res Ctr, Dept Cellular Biotechnol, Esfahan 8165131378, Iran; [Homayouni Moghadam, Farshad] Univ Tehran Med Sci, Endocrinol & Metab Clin Sci Inst, Endocrinol & Metab Res Ctr, Tehran 1411713137, Iran in 2021.0, Cited 32.0. Product Details of 99-61-6. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

A novel series of tacrine based cyclopentapyranopyridine- and tetrahydropyranoquinoline-kojic acid derivatives were designed, synthesized, and evaluated as anti-cholinesterase agents. The chemical structures of all target compounds were characterized by H-1-NMR, C-13-NMR, and elemental analyses. The synthesized compounds mostly inhibited acetylcholinesterase enzyme (AChE) with IC50 values of 4.18-48.71 mu M rather than butyrylcholinesterase enzyme (BChE) with IC50 values of >100 mu M. Among them, cyclopentapyranopyridine-kojic acid derivatives showed slightly better AChE inhibitory activity compared to tetrahydropyranoquinoline-kojic acid. The compound 10-amino-2-(hydroxymethyl)-11-(4-isopropylphenyl)-7,8,9,11-tetrahydro-4H-cyclopenta[b]pyrano[2 ‘,3 ‘ : 5,6]pyrano[3,2-e]pyridin-4-one (6f) bearing 4-isopropylphenyl moiety and cyclopentane ring exhibited the highest anti-AChE activity with IC50 value of 4.18 mu M. The kinetic study indicated that the compound 6f acts as a mixed inhibitor and the molecular docking studies also illustrated that the compound 6f binds to both the catalytic site (CS) and peripheral anionic site (PAS) of AChE. The compound 6f showed moderate neuroprotective properties against H2O2-induced cytotoxicity in PC12 cells. The theoretical ADME study also predicted good drug-likeness for the compound 6f. Based on these results, the compound 6f seems to be a very promising AChE inhibitor for the treatment of Alzheimer’s disease.

Product Details of 99-61-6. Welcome to talk about 99-61-6, If you have any questions, you can contact Babaee, S; Chehardoli, G; Akbarzadeh, T; Zolfigol, MA; Mahdavi, M; Rastegari, A; Moghadam, FH; Najafi, Z or send Email.

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Some scientific research about 99-61-6

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An article Direct Synthesis, Characterization and Theoretical Studies of N-(6-Amino-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)benzamide Derivatives WOS:000612107500027 published article about MONOXIDE-FREE AMINOCARBONYLATION; N-SUBSTITUTED FORMAMIDES; RECEPTOR KINASE 2; URACIL DERIVATIVES; AMIDE-BOND; DIRECT AMIDATION; ALCOHOLS; ARYL; NUCLEOSIDES; INHIBITION in [Das, Tushar; Das, Subrata] Natl Inst Technol Patna, Dept Chem, Patna 800005, Bihar, India; [Ranjan, Amit] Dr DY Patil Vidyapeeth, Dr DY Patil Biotechnol & Bioinformat Inst, Canc & Translat Res Lab, Pune 411033, Maharashtra, India; [Sieron, Leslaw; Maniukiewicz, Waldemar] Lodz Univ Technol, Inst Gen & Ecol Chem, Zeromskiego 116, Lodz, Poland; [Das, Tushar] Natl Inst Pharmaceut Educ & Res Hajipur, Dept Pharmacoinformat, Vaishali 844102, Hajipur, India in 2021, Cited 52. Product Details of 99-61-6. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

With the far-flung importance of uracil and amides in innumerable fields of chemistry and biology, a coherent synthesis that nullifies the use of prodigal reagents, methods and catalysts are hugely accepted. From the present outcomes, we report a highly atom profitable nucleophilic addition reaction of aromatic aldehydes and heterocyclic amines for the generation of amides having an excellent yield and high reproducibility. The main force responsible for the forward reaction is the presence of the nitroso group at the C-5 position on uracil scaffold, which drives the formation of formidable range products. The conclusive mechanism is based on the dehydrogenation reaction of the carbinolamine product formed during the nucleophilic addition reaction of the aromatic aldehyde with the free heterocyclic amino group to yield the corresponding amides. The synthesized compounds were predicated for biological properties and proved it to be an ideal G protein-coupled receptor kinase2 (GRK2) inhibitor. Out of all, the compound 3 f showed the most preeminent properties when compared to Paroxetine, studied using molecular docking. At the same time, computed ADME analysis proved them as an ideal drug candidate. Our findings not only prophesize new methods for the synthesis of bioactive-amides using a cross-coupling strategy but also demonstrates their novel applications as a human GRK2 inhibitor.

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An article Synthesis of Fluorinated Poly(phenyl-alkane)s of Intrinsic Microporosity by Regioselective Aldehyde (A(2)) + Aromatics (B-2) Friedel-Crafts Polycondensation WOS:000674278700060 published article about MOLECULAR-SIEVE; POLYMERS; PERFORMANCE; MEMBRANES; SEPARATION in [Zhou, Shengyang; Guan, Jiayu; Li, Ziqin; Zhang, Qifeng; Zheng, Jifu; Li, Shenghai; Zhang, Suobo] Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Ecomat, Changchun 130022, Peoples R China; [Zhou, Shengyang; Guan, Jiayu; Li, Ziqin; Li, Shenghai; Zhang, Suobo] Univ Sci & Technol China, Hefei 230026, Peoples R China in 2021.0, Cited 45.0. COA of Formula: C7H5NO3. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

The design of functionalized porous materials is an important research direction in material science, especially for fluorine-containing materials with enhanced thermal/oxidative stability, lower dielectric constants, and better gas-selective permeation. In this work, a series of poly(phenyl-alkane)s of intrinsic microporosity (PIM-xR) were synthesized by the methanesulfonic acid-catalyzed Friedel-Crafts hydroxyalkylation polycondensation of contorted and rigid multibenzene and benzaldehyde derivatives. The PIM-xR exhibited good thermal stability, excellent solution processability, and high Brunauer-Emmett-Teller (BET) surface areas (400-1200 m(2) g(-1)). The physicochemical properties and applications of PIM-xR could be tuned by the type, quantity, distribution, and postmodification of substituents on the benzaldehyde derivatives. Unlike other contorted and rigid multibenzene derivatives, only electron-rich spirobiindane derivatives directly produced soluble, linear, high-molecular-weight polymers without cross-linking because spirobiindane possesses three t-butyl-like structural units that provide large steric hindrance at potential reactive sites. Subsequently, a series of fluorinated PIMs (PIM-xF) with different fluorine contents and distributions were explored, and the relationship between the microporosity of PIM-xR and degrees of rotational freedom of the polymer chains was analyzed using these PIM-xF. Flexible and transparent PIM-xF membranes were easily obtained by solution processing and exhibited high gas permeabilities and moderate permeability selectivity. In particular, the CO2/N-2 separation performance of the PIM-5F membrane exceeded the 2008 Robeson’s upper bound (P-CO2 = 3240 barrer and alpha((CO2/N2)) = 27.9). This work provides a facile method for the precise design and preparation of fluorinated or other functionalized porous materials for environmental and energy applications.

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About 3-Nitrobenzaldehyde, If you have any questions, you can contact Varzi, Z; Esmaeili, MS; Taheri-Ledari, R; Maleki, A or concate me.. HPLC of Formula: C7H5NO3

HPLC of Formula: C7H5NO3. Authors Varzi, Z; Esmaeili, MS; Taheri-Ledari, R; Maleki, A in ELSEVIER published article about in [Varzi, Zahra; Esmaeili, Mir Saeed; Taheri-Ledari, Reza; Maleki, Ali] Iran Univ Sci & Technol, Dept Chem, Catalysts & Organ Synth Res Lab, Tehran 1684613114, Iran in 2021.0, Cited 55.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

In this study, an efficient hybrid nanocatalyst made of guar gum (guarana, as a natural basis), magnetic iron oxide nanoparticles, and copper(I) oxide nanoparticles (Cu2O NPs) is fabricated and suitably applied for catalyzing the multicomponent (three- and four-component) synthesis reactions of imidazole derivatives. Here, an easy preparation strategy for this novel catalytic system (Cu2O/Fe3O4@guarana) is presented. Then, the application of this catalytic system for the synthesis of imidazole derivatives is precisely investigated. For this purpose, ultrasonication is introduced as an efficient and fast method. In summary, the high catalytic efficiency of Cu2O/Fe3O4@guarana nanocomposite is well demonstrated by high reaction yields obtained in the presence of a small amount of this nanocomposite, under mild conditions. Wide active surface area, substantial magnetic behavior, excellent heterogeneity, suitable stability, well reusability, and etc. have distinguished this catalytic system as an instrumental tool for facilitating the complex synthetic reactions.

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Welcome to talk about 99-61-6, If you have any questions, you can contact Aghaei-Hashjin, M; Yahyazadeh, A; Abbaspour-Gilandeh, E or send Email.. Formula: C7H5NO3

An article Zr@IL-Fe3O4 MNPs as an efficient and green heterogeneous magnetic nanocatalyst for the one-pot three-component synthesis of highly substituted pyran derivatives under solvent-free conditions WOS:000671447100034 published article about RECYCLABLE CATALYST; SEPARABLE CATALYST; AMMONIUM BROMIDE; IONIC LIQUID; ACID; NANOPARTICLES; MULTICOMPONENT; WATER; TETRAHYDROBENZOPYRAN; PARTICLES in [Aghaei-Hashjin, Mehraneh; Yahyazadeh, Asieh] Univ Guilan, Chem Dept, Rasht 413351914, Iran; [Abbaspour-Gilandeh, Esmayeel] Univ Mohaghegh Ardabili, Coll Sci, Dept Chem, Ardebil, Iran in 2021.0, Cited 68.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6. Formula: C7H5NO3

The present study was conducted to synthesize Zr@IL-Fe3O4 MNPs as a new magnetically recoverable heterogeneous catalyst, which was then characterized by Fourier transform infrared (FT-IR) spectroscopy, energy dispersive X-ray spectroscopy (EDX), vibrating sample magnetometry (VSM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) techniques. The catalytic behavior of the Zr@IL-Fe3O4 MNPs was efficiently used for the synthesis of highly substituted pyran derivatives via a one-pot three-component condensation of 4-hydroxycoumarin/dimedone, malononitrile, and arylaldehydes under solvent-free conditions. This new methodology demonstrated some important features, including short reaction times, excellent yields, lower loading of the catalyst, easy work-up, and recyclability of the catalyst for a minimum of six times without any noticeable decrease in catalytic activity.

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