Tag: M.W=150-200

I found the field of Plant Sciences; Chemistry; Pharmacology & Pharmacy very interesting. Saw the article Bioactive naphthoquinone and anthrone derivatives from endophytic Micromonospora sp. NEAU-gq13 published in 2019. Category: thiomorpholine, Reprint Addresses Wang, JD (corresponding author), Zhejiang Hisun Pharmaceut Co Ltd, Zhejiang Key Lab Antifungal Drugs, Taizhou 318000, Peoples R China.; Xiang, WS (corresponding author), Northeast Agr Univ, Sch Life Sci, Life Sci & Biotechnol Res Ctr, Harbin 150030, Heilongjiang, Peoples R China.. The CAS is 90-44-8. Through research, I have a further understanding and discovery of Anthrone

Two new naphthalenone derivatives, 5-hydroxy-4-oxo-2-(2-oxopropyl)-1,2,3,4-tetrahydronaphthalen-1-yl acetate (1) and 5-hydroxy-2-(2-hydroxypropyl)naphthalene-1,4-dione (2), together with two new anthrone derivatives, (S)-2,5-dihydroxy-2-methyl-1,2,3,4-tetrahydroanthracene-9,10-dione (3) and 4,5-dihydroxy-2-methyl-9H-xanthen-9-one (4), were isolated from the fermentation broth of endophytic Micromonospora sp. NEAU-gq13. Their structures were determined by 1D-NMR, 2D-NMR, and HR-ESI-MS analysis. Compounds 2 and 3 exhibited strong cytotoxic activity against human central nervous system cancer (SF-268) with the IC50 values of 3.04 and 5.66 mu g/ml, respectively. Moreover, compound 2 also displayed potent activity against human liver cancer (HepG2) with an IC50 value of 1.01 mu g/ml.

About Anthrone, If you have any questions, you can contact Li, JS; Zhang, H; Qi, H; Wang, JD; Xiang, WS or concate me.. Category: thiomorpholine

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

In 2021 COLLOID SURFACE A published article about ONE-POT SYNTHESIS; IONIC LIQUID; EFFICIENT NANOCATALYST; SHELL MICROSPHERES; SILICA MATERIALS; MOLECULAR-SIEVE; CATALYST; CORE; NANOPARTICLES; NANOCOMPOSITES in [Shaker, Masoumeh; Elhamifar, Dawood] Univ Yasuj, Dept Chem, Yasuj 7591874831, Iran in 2021, Cited 107. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6. Application In Synthesis of 3-Nitrobenzaldehyde

In this study, preparation, characterization and catalytic application of a novel core-shell structured magnetic Tiloaded phenylene-based nanoporous organosilica (Mag@Ti-NOS) nanocomposite are developed. The Mag@TiNOS was synthesized via cetyltrimethylammonium bromide (CTAB) directed co-condensation of tetramethoxysilane (TMOS), tetrabutyl orthotitanate (TBOT) and 1,4-bis(triethoxysilyl)benzene (BTEB) over Mag@ SiO2 under alkaline conditions. This nanocomposite was characterized by using FT-IR, EDX, PXRD, VSM, SEM, TEM, XPS, ICP and TGA techniques. These analyses showed a core-shell structure with high chemical and thermal stability for the designed material. The Mag@Ti-NOS nanocomposite was employed as an effective, powerful and recyclable catalyst in the synthesis of tetrahydrobenzo[b]pyrans in H2O at 50 degrees C under ultrasonic conditions. This catalyst was recovered and reused several times without significant decrease in efficiency and stability. The recovered catalyst was analyzed by FT-IR, PXRD and SEM to study its stability during reaction process.

About 3-Nitrobenzaldehyde, If you have any questions, you can contact Shaker, M; Elhamifar, D or concate me.. Application In Synthesis of 3-Nitrobenzaldehyde

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

Recommanded Product: 99-61-6. Recently I am researching about IMINIUM ION CYCLIZATION; CARBONYL METATHESIS; O-ALKYNYLANILINES; CONSTRUCTION; BASICITY; HETEROCYCLES; ALDEHYDES; INDOLINE; RULES; WATER, Saw an article supported by the . Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Amemiya, S; Okemoto, S; Tsubouchi, A; Saito, A. The CAS is 99-61-6. Through research, I have a further understanding and discovery of 3-Nitrobenzaldehyde

We developed a synthetic method for alpha-(aminoethyl)-alpha,beta-enones from aryl-substituted homopropargyl sulfonamides and aldehydes, representing the first synthesis of conjugated enones via alkyne aza-Prins cyclization. These products could be converted into pyrrolidines by a formal 5-endo-trig cyclization.

About 3-Nitrobenzaldehyde, If you have any questions, you can contact Amemiya, S; Okemoto, S; Tsubouchi, A; Saito, A or concate me.. Recommanded Product: 99-61-6

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

Authors Ghosh, T; Mohammad, A; Mobin, SM in AMER CHEMICAL SOC published article about PALLADIUM-CATALYZED CYANATION; AEROBIC OXIDATIVE CONVERSION; REDUCTIVE AMINATION; HIGHLY EFFICIENT; ARYL BROMIDES; NITRILES; ALDEHYDES; ACID; NANOPARTICLES; ALCOHOLS in [Ghosh, Topi; Mohammad, Akbar; Mobin, Shaikh M.] Indian Inst Technol Indore, Discipline Chem, Khandwa Rd, Indore 453552, Madhya Pradesh, India; [Mobin, Shaikh M.] Indian Inst Technol Indore, Discipline Met Engn & Mat Sci, Khandwa Rd, Indore 453552, Madhya Pradesh, India; [Mobin, Shaikh M.] Indian Inst Technol Indore, Discipline Biosci & Biomed Engn, Khandwa Rd, Indore 453552, Madhya Pradesh, India in 2019, Cited 91. Recommanded Product: 104-21-2. The Name is 4-Methoxybenzyl acetate. Through research, I have a further understanding and discovery of 104-21-2

Development of a low-cost, environmentally benign and robust catalyst for multipurpose industrially relevant organic transformations is highly desirable for the sustainable future of chemical industries. A hybrid cobalt doped-cerium oxide nanocatalyst (Co@CeO2NC) was prepared via simple coprecipitation method using water as the solvent. The characterization of Co@CeO2NC was performed using different techniques such as XRD, TGA, FE-SEM, HR-TEM, EDAX-mapping, BET, and XPS analysis. The structural characterization of the prepared sample by XRD and XPS analysis revealed the presence of the mixed phase of cobalt oxide and cobalt doped-cerium oxide as a hybrid (Co@CeO2NC). Industrially relevant organic transformations such as (i) nitrile formation using aldehyde with hydroxyl amine hydrochloride, (ii) reductive amination of aldehydes to form tertiary N,N-dimethyl amines, and (iii) direct acetylation of alcohols/amines with acetic acid were achieved in an excellent manner using Co@CeO2NC hybrid as the multifunctional catalyst. Excellent catalytic activity of Co@CeO2NC was noticed for the conversion of 4-chlorobenzaldehyde to 4-chlorobenzonitrile with 99% conversion and 99% selectivity and 100% conversion of benzaldehyde to N,N-dimethylbenzylamine using DMF as NMe2 source, reductant, and solvent. Moreover, acetylation of 4-methoxybenzyl alcohol and 2-methyl aniline gave excellent conversion and selectivity toward the formation of -O and -N acetyl. The scope of the Co@CeO2NC was further evaluated for other aldehydes, alcohols, and amines with an excellent conversion and high selectivity.

About 4-Methoxybenzyl acetate, If you have any questions, you can contact Ghosh, T; Mohammad, A; Mobin, SM or concate me.. Recommanded Product: 104-21-2

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

I found the field of Chemistry very interesting. Saw the article Sequential four-component protocol for the synthesis of pyrido[1,2-a]pyrimidin-6-one derivatives in water published in 2021.0. Safety of 3-Nitrobenzaldehyde, Reprint Addresses Rezvanian, A (corresponding author), Alzahra Univ, Dept Chem & Phys, POB 1993891176, Tehran, Iran.. The CAS is 99-61-6. Through research, I have a further understanding and discovery of 3-Nitrobenzaldehyde

A highly efficient and environmentally benign synthesis of N-fused heterocyclic compounds including pyrido[1,2-a]pyrimidine-6-one moiety is successfully achieved via a sequential four-component reaction. The process involves the formation of diversely substituted 9-nitro-1,2,3,4,7,8-hexahydro-6H-pyrido[1,2-a]pyrimidin-6-ones from the reaction of Meldrum’s acid, benzaldehydes, 1,1-bis(methylthio)-2-nitroethylene and various diamines in the presence of p-toluene sulfonic acid (PTSA) as an acidic catalyst in water as a green solvent. The salient features of the present methodology are easily available starting materials, the use of water as environmentally benign solvent, simple execution, applicable to a wide range of starting materials and good to excellent yields.

About 3-Nitrobenzaldehyde, If you have any questions, you can contact Rezvanian, A; Amoozadkhalili, F; Roosta, A or concate me.. Safety of 3-Nitrobenzaldehyde

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

Authors Bouhrim, M; Ouassou, H; Loukili, E; Ramdani, M; Mekhfi, H; Ziyyat, A; Legssyer, A; Aziz, M; Bnouham, M in WOLTERS KLUWER MEDKNOW PUBLICATIONS published article about ANTIOXIDANT; EXTRACT; GLUCOSE; METABOLISM in [Bouhrim, Mohamed; Ouassou, Hayat; Loukili, El Hassania; Ramdani, Mohammed; Mekhfi, Hassane; Ziyyat, Abderrahim; Legssyer, Abdelkhaleq; Aziz, Mohammed; Bnouham, Mohamed] Univ Mohamed First, Fac Sci, Oujda, Morocco in 2019, Cited 39. HPLC of Formula: C14H10O. The Name is Anthrone. Through research, I have a further understanding and discovery of 90-44-8

Objective: To assess the antidiabetic effect of Opuntia dillenii seed oil on rats with diabetes mellitus. Methods: A rat diabetes model was established by intraperitoneal injection of rats with 50 mg/kg streptozotocin. Thirty albino Wistar rats were divided into five groups: the diabetic control group and normal control group were treated only with distilled water, two diabetic groups received 1 and 2 mL/kg of oil per day, respectively, for 30 days and one diabetic group received 2 mg/kg of glibenclamide. In addition, blood glucose was determined weekly. Body weight, average daily food, water intake and urinary volume of each animal were determined before and after the treatment period. After the treatment period, hepatic glycogen was determined using the anthrone reagent, and glycosuria, total cholesterol, triglycerides, alanine aminotransferase, aspartate aminotransferase, urea, creatinine and uric acid were estimated using common clinical diagnostic kits. Results: Oral intake of the oil at 1 and 2 mL/kg for the diabetic animals significantly diminished blood glucose, glycosuria, total cholesterol, triglycerides, alanine aminotransferase, aspartate aminotransferase, urea, creatinine and uric acid, accompanied by a noticeable elevation in the amount of hepatic glycogen in comparison with the diabetic control group. Similarly, Opuntia dillenii seed oil significantly increased the food intake and decreased the urinary volume per day in treated rats of the same groups in comparison with the period before the treatment intervention and attenuated body weight loss in the diabetic rats. Moreover, this effect of the oil was dose dependent. On the other hand, the oil did not affect their need for water. Conclusions: The results show that Opuntia dillenii seed oil has a very important antidiabetic effect on streptozotocin-induced diabetic rats. Hence, we suggest it as a preventive control of diabetes mellitus.

HPLC of Formula: C14H10O. About Anthrone, If you have any questions, you can contact Bouhrim, M; Ouassou, H; Loukili, E; Ramdani, M; Mekhfi, H; Ziyyat, A; Legssyer, A; Aziz, M; Bnouham, M or concate me.

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

An article Visible-light-induced oxidative coupling of vinylarenes with diselenides leading to alpha-aryl and alpha-alkyl selenomethyl ketones WOS:000629630600031 published article about DIPHENYL DISELENIDE; ALDEHYDES; SELENIDES; OLEFINS in [Liu, Gong-Qing; Yi, Wei; Wang, Peng-Fei; Liu, Ji; Ma, Meng; Hao, Da-Yun; Ming, Liang; Ling, Yong] Nantong Univ, Sch Pharm, 19 Qixiu Rd, Nantong 226001, Peoples R China in 2021.0, Cited 98.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9. Safety of Benzophenone

A visible-light-induced oxidative coupling of diselenides with readily available vinylarenes is demonstrated. This benign protocol allows one to access a wide range of alpha-aryl and alpha-alkyl selenomethyl ketones in good yields with excellent functional group compatibility. The distinct advantages of this protocol over all previous methods include the use of a green solvent and air as an oxidant and the lack of a photocatalyst, a base, and an oxidant as well as better green chemistry matrices. Furthermore, the title reaction can be performed with natural sunlight, the most sustainable energy source imaginable. Additionally, the mild reaction conditions, easy operation and suitability for the modification of styrene-functionalized biomolecules make the current reaction system a more attractive method for the synthesis of a variety of medicinal and agrochemical compounds of interest.

Safety of Benzophenone. About Benzophenone, If you have any questions, you can contact Liu, GQ; Yi, W; Wang, PF; Liu, J; Ma, M; Hao, DY; Ming, L; Ling, Y or concate me.

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

I found the field of Chemistry very interesting. Saw the article On/Off O-2 Switchable Photocatalytic Oxidative and Protodecarboxylation of Carboxylic Acids published in 2019. HPLC of Formula: C14H10O, Reprint Addresses Hosseini-Sarvari, M (corresponding author), Shiraz Univ, Dept Chem, Shiraz 7194684795, Iran.. The CAS is 90-44-8. Through research, I have a further understanding and discovery of Anthrone

Photoredox catalysis in recent years has manifested a powerful branch of science in organic synthesis. Although merging photoredox and metal catalysts has been a widely used method, switchable heterogeneous photoredox catalysis has rarely been considered. Herein, we open a new window to use a switchable heterogeneous photoredox catalyst which could be turned on/off by changing a simple stimulus (O-2) for two opponent reactions, namely, oxidative and protodecarboxylation. Using this strategy, we demonstrate that Au@ZnO core-shell nanoparticles could be used as a switchable photocatalyst which has good catalytic activity to absorb visible light due to the localized surface plasmon resonance effect of gold, can decarboxylate a wide range of aromatic and aliphatic carboxylic acids, have multiple reusability, and are a reasonable candidate for synthesizing both aldehydes/ketones and alkane/arenes in a large-scale set up. Some biologically active molecules are also shown via examples of the direct oxidative and protodecarboxylation which widely provided pharmaceutical agents.

HPLC of Formula: C14H10O. About Anthrone, If you have any questions, you can contact Bazyar, Z; Hosseini-Sarvari, M or concate me.

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

An article Azolium/Hydroquinone Organo-Radical Co-Catalysis: Aerobic C-C-Bond Cleavage in Ketones WOS:000608268400001 published article about SINGLE-ELECTRON-TRANSFER; ALPHA-HYDROXYLATION; NMR-SPECTROSCOPY; CHEMILUMINESCENCE; ORGANOCATALYSIS; CHEMISTRY; ACID; OXIDATIONS; PHOTOLYSIS; STRATEGIES in [Nakatsuji, Yuya; Masuda, Sakyo; Takemoto, Yoshiji] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, 46-29 Shimoadachi Cho, Kyoto 6068501, Japan; [Kobayashi, Yusuke] Kyoto Pharmaceut Univ, Dept Pharmaceut Chem, Yamashina Ku, 1 Misasagishichono Cho, Kyoto 6078412, Japan in 2021.0, Cited 77.0. Application In Synthesis of Benzophenone. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

Organo-radical catalysts have recently attracted great interest, and the development of this field can be expected to broaden the applications of organocatalysis. Herein, the first example of a radical-generating system is reported that does not require any photoirradiation, radical initiators, or preactivated substrates. The oxidative C-C-bond cleavage of 2-substituted cyclohexanones was achieved using an azolium salt and a hydroquinone as co-catalysts. A catalytic mechanism was proposed based on the results of diffusion-ordered spectroscopy and cyclic voltammetry measurements, as well as computational studies.

About Benzophenone, If you have any questions, you can contact Nakatsuji, Y; Kobayashi, Y; Masuda, S; Takemoto, Y or concate me.. Application In Synthesis of Benzophenone

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

In 2021.0 J AM CHEM SOC published article about O BOND ACTIVATION; MOLECULAR-OXYGEN; SELECTIVE OXIDATION; SINGLET OXYGEN; C=C BONDS; COMPLEX; DIOXYGEN; OLEFINS; REACTIVITY; IRON in [Huang, Zhiliang; Guan, Renpeng; Bennett, Elliot L.; Robertson, Craig M.; Xiao, Jianliang] Univ Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, England; [Shanmugam, Muralidharan; Brookfield, Adam; McInnes, Eric J. L.] Univ Manchester, Dept Chem, Manchester M13 9PL, Lancs, England; [Shanmugam, Muralidharan; Brookfield, Adam; McInnes, Eric J. L.] Univ Manchester, Photon Sci Inst, Manchester M13 9PL, Lancs, England in 2021.0, Cited 58.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9. SDS of cas: 119-61-9

The oxidative cleavage of C = C double bonds with molecular oxygen to produce carbonyl compounds is an important transformation in chemical and pharmaceutical synthesis. In nature, enzymes containing the first-row transition metals, particularly heme and non-heme iron-dependent enzymes, readily activate O-2 and oxidatively cleave C = C bonds with exquisite precision under ambient conditions. The reaction remains challenging for synthetic chemists, however. There are only a small number of known synthetic metal catalysts that allow for the oxidative cleavage of alkenes at an atmospheric pressure of O-2, with very few known to catalyze the cleavage of nonactivated alkenes. In this work, we describe a light-driven, Mn-catalyzed protocol for the selective oxidation of alkenes to carbonyls under 1 atm of O-2. For the first time, aromatic as well as various nonactivated aliphatic alkenes could be oxidized to afford ketones and aldehydes under clean, mild conditions with a first row, biorelevant metal catalyst. Moreover, the protocol shows a very good functional group tolerance. Mechanistic investigation suggests that Mn-oxo species, including an asymmetric, mixed-valent bis(mu-oxo)-Mn(III,IV) complex, are involved in the oxidation, and the solvent methanol participates in O-2 activation that leads to the formation of the oxo species.

SDS of cas: 119-61-9. About Benzophenone, If you have any questions, you can contact Huang, ZL; Guan, RP; Shanmugam, M; Bennett, EL; Robertson, CM; Brookfield, A; McInnes, EJL; Xiao, JL or concate me.

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