Category: 99-61-6

Computed Properties of C7H5NO3. Authors Ma, RN; Xiao, ZY; Zhong, W; Lu, CX; Shen, ZQ; Zhao, D; Liu, XM in WILEY published article about in [Ma, Ruonan; Xiao, Zhiyin; Zhong, Wei; Lu, Chunxin; Shen, Zhongquan; Liu, Xiaoming] Jiaxing Univ, Coll Biol Chem Sci & Engn, Jiaxing 314001, Peoples R China; [Ma, Ruonan; Zhao, Dan; Liu, Xiaoming] Nanchang Univ, Sch Chem, Nanchang 330031, Jiangxi, Peoples R China in 2021.0, Cited 35.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

Cuprous halides, best described as (CuX)(n) (X = Cl-, Br-, and I-) in their solid state, catalyse selective aerobic oxidation of alcohols with the assistance of both NMI (N-methylimidazole) and TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl), and the iodide generally demonstrates the highest activity, for example, in the oxidation of 1-octanol at ambient temperature under 24 h’ reaction. However, in the aerobic oxidation of benzylic alcohols, the chloride showed superiority to the iodide in that the aerobic oxidation was quantitatively completed within 3 h at ambient temperature whereas the iodide showed only about half the activity of the chloride analogue. By probing the system using electrochemistry, electric conductivity, and H-1 NMR titration, it was revealed that the surprising anomaly was due to the difference in the rate of forming active species, [Cu (NMI)(2)X(MeCN)], from the polymeric solid in a two-stage process. Substrates expansion of 11 benzylic alcohols indicated that CuCl/NMI/TEMPO system demonstrated quantitative conversion of benzylic alcohols into corresponding aldehydes within 3 h and showed great tolerance to the substituents on the phenyl ring of the substrates. Furthermore, electron-withdrawing substituent was beneficial to the oxidation and could offset the steric effect at orthro-substituent. Such a behaviour suggested that in the catalysis, increasing the acidity of the hydroxyl group (OH) of the substrates could ease the oxidation, which implied that the deprotonation via an internal pathway might be one of the rate-determining steps. Our results also showed that the anion halide participated actively in the catalysis by coordinating to Cu(I) in the active species.

About 3-Nitrobenzaldehyde, If you have any questions, you can contact Ma, RN; Xiao, ZY; Zhong, W; Lu, CX; Shen, ZQ; Zhao, D; Liu, XM or concate me.. Computed Properties of C7H5NO3

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Formula: C7H5NO3. Authors Gilanizadeh, M; Zeynizadeh, B in TAYLOR & FRANCIS LTD published article about in [Gilanizadeh, Masumeh; Zeynizadeh, Behzad] Urmia Univ, Fac Chem, Orumiyeh 5756151818, Iran in 2021, Cited 45. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

An efficient green method has been developed for the cascade multi-component Hantzsch reaction of acridinediones and biscoumarins using Fe3O4@SiO2@Ni-Zn-Fe layered double hydroxide (LDH). Nano Ni-Zn-Fe LDH immobilized on silica-layered magnetite was synthesized via a simple co-precipitation procedure, and characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD) and transmission electron microscopy (TEM). The nanocatalyst has the usual features of Fe3O4@SiO2 and Ni-Zn-Fe LDH. Moreover, it contains magnetism properties which is related to the presence of magnetite in the nanocatalyst and can be easily separated from the reaction mixture with an external magnetic field. Subsequently, the nanomagnetic-LDH was used to evaluate catalytic activity with the tandem synthesis of acridinedione and biscoumarin derivatives. The mesoporous catalyst showed excellent performance for multi-component reactions between aromatic aldehydes, 4-hydroxycoumarin, and dimedone and ammonium acetate. Acridinediones were provided within 15-35 min in 80-96% yields under solvent-free conditions in 70-80 degrees C and also, biscoumarins were obtained within 1-40 min in 87-95% yields under reflux conditions in water. The present study includes noteworthy advantages of mild reaction conditions, short times of reaction, absence of hazardous and expensive organic solvents and reagents, presence of water as an eco-friendly solvent, using green nanomagnetic-LDH and the ability to recycle the nanocatalyst.

Formula: C7H5NO3. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Gilanizadeh, M; Zeynizadeh, B or concate me.

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Thiomorpholine – Wikipedia,
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Abdolmohammadi, S; Afsharpour, M in [Abdolmohammadi, Shahrzad] Islamic Azad Univ, East Tehran Branch, Dept Chem, POB 18735-138, Tehran, Iran; [Afsharpour, Maryam] Res Ctr Iran, Dept Inorgan Chem Chem & Chem Engn, Tehran, Iran published An ultrasound assisted cyclocondensation reaction for the efficient synthesis of [1]benzopyranopyrido[d]pyrimidines using porous graphene/MoO3 in 2021, Cited 96. Recommanded Product: 99-61-6. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6.

In this paper, we report a feasible protocol for the preparation of [1]benzopyranopyrido[d]pyrimidines via expeditious sonochemical route. The reaction efficiency was evaluated by influence of several parameters including sonication power, sonication time, different solvents, and using porous graphene/MoO3 nanocomposite as catalyst, for the first time. The effect of the ultrasonication comparing with the conventional heating on the synthesis of the titled compounds shows that the ultrasonic irradiation is required to rich the cyclized products. The structural properties of porous graphene/MoO3 nanocomposite were determined by Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffractometry (XRD), scanning electron microscope (SEM), Raman spectroscopy, and also by TGA analysis. Confirmation of the structures of compounds 4a-4h were also established with IR, H-1 NMR, and C-13 NMR spectroscopic data and also by elemental analyses.

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Safety of 3-Nitrobenzaldehyde. Authors Khoshdel, MA; Shirini, F; Langarudi, MSN; Zabihzadeh, M; Biglari, M in ROYAL SOC CHEMISTRY published article about in [Alipour Khoshdel, Meysam; Shirini, Farhad; Nikoo Langarudi, Mohaddeseh Safarpoor; Zabihzadeh, Mehdi; Biglari, Mohammad] Univ Guilan, Dept Chem, Coll Sci, Rasht 4133519141, Iran in 2021.0, Cited 44.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

The development of environmentally benign synthetic protocols has attracted increasing attention in recent organic syntheses. As a part of this concept, our group synthesized a new natural deep eutectic solvent (NADES) by using gabapentin and choline chloride. After characterization by FTIR, H-1 and C-13 NMR, and mass spectra, the prepared NADES was utilized as an efficacious catalyst for the synthesis of 4H-pyran scaffolds such as tetrahydrobenzo[b]pyran and pyrano[2,3-d]pyrimidinone(thione) derivatives. The use of inexpensive and bio-compatible reagents for the synthesis of the catalyst, a simple and green procedure for the preparation of the catalyst and products, short reaction times, high yields of the products, and applicability to large-scale synthesis are the prominent features of this protocol. Also, the catalyst could be recovered easily and recycled up to five times without significant loss of its catalytic activity.

Safety of 3-Nitrobenzaldehyde. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Khoshdel, MA; Shirini, F; Langarudi, MSN; Zabihzadeh, M; Biglari, M or concate me.

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Thiomorpholine – Wikipedia,
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Quality Control of 3-Nitrobenzaldehyde. Authors Desai, NC; Jadeja, KA; Jadeja, DJ; Khedkar, VM; Jha, PC in TAYLOR & FRANCIS INC published article about in [Desai, Nisheeth C.; Jadeja, Krunalsinh A.; Jadeja, Dharmpalsinh J.] Maharaja Krishnakumarsinhji Bhavnagar Univ, Dept Chem DST FIST Sponsored & UGC NON SAP, Div Med Chem, Mahatma Gandhi Campus, Bhavnagar, Gujarat, India; [Khedkar, Vijay M.] Vishwakarma Univ, Sch Pharm, Dept Pharmaceut Chem, Pune, Maharashtra, India; [Jha, Prakash C.] Cent Univ Gujarat, Sch Appl Mat Sci, Gandhinagar, India in 2021, Cited 42. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

A series of 5-aryl-3-(4-oxo-2-phenylquinazolin-3(4H)-yl)-2-(pyridin-4-yl)thiazolidin-4-ones were synthesized and evaluated for their antibacterial and antifungal activities. Various spectral techniques e.g., IR, H-1 NMR, C-13 NMR and Mass spectrometry were used to determine structure of novel synthesized compounds. The title compounds showed good to excellent inhibition potency for respective Gram-positive bacterial strains and Gram-negative bacterial strains. These compounds exhibited a broad spectrum of inhibitory activity. Molecular docking studies against microbial DNA gyrase sub unit B could provide valuable insights into the binding affinity of these molecules and their plausible mechanism of antimicrobial action. Compounds 5a, 5d, 5f and 5h, 5i, 5j, 5o exhibited excellent activity against bacterial and fungal strains respectively.

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Thiomorpholine – Wikipedia,
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Category: thiomorpholine. I found the field of Chemistry very interesting. Saw the article Synthesis, structure, characterization and biological evaluation of 3-substituted 1-pyridin-2-ylimidazo[1,5-a]pyridine-based copper(I)-phosphine complexes for anticancer drug screening published in 2021, Reprint Addresses Velusamy, M (corresponding author), North Eastern Hill Univ, Dept Chem, Shillong 793022, Meghalaya, India.; Murali, M (corresponding author), Natl Coll Autonomous, Dept Chem, Coordinat & Bioinorgan Chem Res Lab, Tiruchirappalli 620001, Tamil Nadu, India.. The CAS is 99-61-6. Through research, I have a further understanding and discovery of 3-Nitrobenzaldehyde.

Copper(I) complexes of the types [Cu(N-N)(PPh3)(2)]NO3(LC41-LC44) and [Cu(N-N)(PPh3)(NO3)] (LC45) carrying 3-substituted 1-pyridine-2-ylimidazo[1,5-a]pyridine (N-N) derivatives and triphenylphosphine (PPh3) ligands have been prepared. The synthesized copper(I)-phosphine complexes were fully characterized by NMR, IR, ESI-MS and UV-visible spectroscopy as well as by cyclic voltammetry. Selected structures such as LC42, LC43 and LC45 were additionally analysed by single-crystal X-ray method, which show that copper(I) centre adopts a highly distorted tetrahedral geometry. The(1)H and(13)C NMR spectral data of the complexes throw light on the nature of metal-ligand bonding. They display d pi-pi* metal-to-ligand charge transfer (MLCT) transition and show quasireversible Cu-I/Cu(II)metal oxidation. Among the copper(I)-phosphine complexes, LC41-LC44 exhibit moderate cytotoxicity (IC50: 24 h, 67-74 mu M; 48 h, 58-70 mu M) against human lung epithelial adenocarcinoma A549 cells, whereas LC45 displays the best activity (IC50: 24 h, 42 mu M; 48 h, 34 mu M) for A549 cancer cell line, which is better than that of the commercial antitumor drug cisplatin. All the complexes also displayed excellent selectivity by being relatively inactive against the human lung epithelial L132 normal cell line with selectivity index (SI) values ranging from 3.4 to 7.4. The complexes block cell cycle progression of A549 cells in G(0)/G(1)phase. FACSVerse analyses are suggestive of reactive oxygen species (ROS) generation and apoptotic cell death induced by the LC41, LC43 and LC45. The induction of apoptosis in A549 cells was shown by Annexin V with propidium iodide (PI) and 4 ‘,6-diamidino-2-phenylindole (DAPI) staining methods and established the ability of LC41, LC43 and LC45 to accumulate in the cell nuclei.

Category: thiomorpholine. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Pathaw, L; Khamrang, T; Selvakumaran, B; Murali, M; Prakash, PA; Jaabir, MSM; Velusamy, M or concate me.

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Thiomorpholine – Wikipedia,
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Recently I am researching about CATALYZED OXIDATIVE SYNTHESIS; ONE-POT SYNTHESIS; 4(3H)-QUINAZOLINONE DERIVATIVES; CASCADE SYNTHESIS; BENZYL ALCOHOLS; QUINAZOLINONES; METAL; EFFICIENT; SILICA; OXIDE, Saw an article supported by the University Grants CommissionUniversity Grants Commission, India; Council of Scientific and Industrial Research, New Delhi, IndiaCouncil of Scientific & Industrial Research (CSIR) – India. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Gupta, R; Arora, G; Yadav, P; Dixit, R; Srivastava, A; Sharma, RK. The CAS is 99-61-6. Through research, I have a further understanding and discovery of 3-Nitrobenzaldehyde. Product Details 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.

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Recommanded Product: 99-61-6. I found the field of Chemistry very interesting. Saw the article Asymmetric Synthesis of 3-Methyleneindolines via Rhodium(I)-Catalyzed Alkynylative Cyclization of N-(o-Alkynylaryl)imines published in 2021.0, Reprint Addresses He, CY; Chu, WD; Liu, QZ (corresponding author), China West Normal Univ, Coll Chem & Chem Engn, Chem Synth & Pollut Control Key Lab Sichuan Prov, Nanchong 637002, Peoples R China.. The CAS is 99-61-6. Through research, I have a further understanding and discovery of 3-Nitrobenzaldehyde.

The first asymmetric synthesis of 3-methyleneindolines from alkynyl imines has been developed via a rhodium-catalyzed tandem process: regioselective alkynylation of the internal alkynes and subsequent intramolecular addition to the imines. The reaction proceeded with unconventional chemo-selectivity and provided 3-methyleneindolines with good yields (up to 82% yield) and high enantioselectivities (up to 97% ee). Moreover, this transformation also features mild reaction conditions, perfect atom economy, and a broad substrate scope.

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Thiomorpholine – Wikipedia,
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Bhat, MA; Naglah, AM; Ansari, SA; Al-Tuwajiria, HM; Al-Dhfyan, A in [Bhat, Mashooq A.; Ansari, Siddique Akber; Al-Tuwajiria, Hanaa M.] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, Riyadh 11451, Saudi Arabia; [Naglah, Ahmed M.] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, Drug Explorat & Dev Chair DEDC, Riyadh 11451, Saudi Arabia; [Naglah, Ahmed M.] Natl Res Ctr, Peptide Chem Dept, Chem Ind Res Div, Cairo 12622, Egypt; [Al-Dhfyan, Abdullah] King Saud Univ, Coll Pharm, Dept Pharmacol & Toxicol, Riyadh 11451, Saudi Arabia; [Al-Dhfyan, Abdullah] King Faisal Specialized Hosp, Res Ctr, Stem Cell & Tissue Reengn Program, MBC 03,POB 3354, Riyadh 11211, Saudi Arabia published ChCl: Gly (DESs) Promote Environmentally Benign Synthesis of Xanthene Derivatives and Their Antitubercular Activity in 2021.0, Cited 59.0. 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 ChCl: Gly (DESs) promoted environmentally benign method was developed for the first time using the reaction of aryl aldehydes and dimedone to give excellent yields of xanthene analogues. The major application of this present protocol is the use of green solvent, a wide range of substrate, short reaction times, ease of recovery, the recyclability of the catalyst, high reaction yield, and ChCl: Gly as an alternative catalyst and solvent. In addition to this, all the synthesized compounds were evaluated for their in vitro antimycobacterial activity against M. tuberculosis H37Ra (MTB) and M. bovis BCG strains. The compounds 3d, 3e, 3f, and 3j showed significant antitubercular activity against MTB and M. bovis strains with minimum inhibitory concentration (MIC) values of 2.5-15.10 mu g/mL and 0.26-14.92 mu g/mL, respectively. The compounds 3e, 3f, and 3j were found to be nontoxic against MCF-7, A549, HCT 116, and THP-1 cell lines. All the prepared compounds were confirmed by H-1 NMR and C-13 NMR analysis.

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Thiomorpholine – Wikipedia,
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An article MIL-101(Cr), an Efficient Heterogeneous Catalyst for One Pot Synthesis of 2,4,5-tri Substituted Imidazoles under Solvent Free Conditions WOS:000643425900001 published article about METAL-ORGANIC FRAMEWORK; TRISUBSTITUTED IMIDAZOLES; HIGHLY EFFICIENT; MOFS; CONVERSION; OXIDATION in [Manteghi, Faranak; Zakeri, Fatemeh] Iran Univ Sci & Technol, Dept Chem, Res Lab Inorgan Chem & Environm, Tehran 1684613114, Iran; [Guy, Owen James] Swansea Univ, Coll Sci, Dept Chem, Singleton Pk, Swansea SA2 8PP, W Glam, Wales; [Tehrani, Zari] Swansea Univ, Coll Engn, Ctr NanoHlth, Inst Life Sci 2, Singleton Pk, Swansea SA2 8PP, W Glam, Wales in 2021, Cited 47. Safety of 3-Nitrobenzaldehyde. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

A chromium-containing metal-organic framework (MOF), MIL-101 (Chromium(III) benzene-1,4-dicarboxylate), was used to catalyze the one pot, three component synthesis of some 2,4,5-trisubstituted imidazoles under solvent-free conditions. The advantages of using this heterogeneous catalyst include short reaction time, high yields, easy and quick isolation of catalyst and products, low amount of catalyst needed, and that the addition of solvent, salt, and additives are not needed. This catalyst is highly efficient and can be recovered at least 5 times with a slight loss of efficiency. The structure of the metal-organic frameworks (MOF) was confirmed by X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). Fourier transform infrared spectroscopy (FTIR) and proton nuclear magnetic resonance (HNMR) were performed to confirm some of the synthesized products. Experimental data indicated that the optimum amount of catalyst was 5 mg for benzil (1 mmol), 4-chlorobenzaldehyde (1 mmol), and ammonium acetate (2.5 mmol), and the synthetic route to the various imidazoles is performed in 10 min by 95% yield, an acceptable result rivalling those of other catalysts.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem