Tag: M.W=150-200

Computed Properties of C10H12O3. McClelland, DJ; Galebach, PH; Motagamwala, AH; Wittrig, AM; Karlen, SD; Buchanan, JS; Dumesic, JA; Huber, GW in [McClelland, Daniel J.; Galebach, Peter H.; Motagamwala, Ali Hussain; Dumesic, James A.; Huber, George W.] Univ Wisconsin, Dept Chem & Biol Engn, Madison, WI 53706 USA; [Motagamwala, Ali Hussain; Karlen, Steven D.; Dumesic, James A.] Wisconsin Energy Inst, Great Lakes Bioenergy Res Ctr, Madison, WI USA; [Wittrig, Ashley M.; Buchanan, J. Scott] ExxonMobil Res & Engn Co, Annandale, NJ USA; [Karlen, Steven D.] Univ Wisconsin, Dept Biochem, 420 Henry Mall, Madison, WI 53705 USA published Supercritical methanol depolymerization and hydrodeoxygenation of lignin and biomass over reduced copper porous metal oxides in 2019, Cited 43. The Name is 4-Methoxybenzyl acetate. Through research, I have a further understanding and discovery of 104-21-2.

Supercritical methanol depolymerization and hydrodeoxygenation (SCM-DHDO) of maple wood and lignin extracted with GVL from maple wood, was studied using a copper porous metal oxide catalyst. Phenols (P or H), guaiacols (G), and syringols (S) with deoxygenated 1 to 3-carbon (C-1-C-3) alkyl tails were the early products (15 min reaction time) from both the maple wood and the GVL extracted lignin. Furthermore, at 15 min reaction time, the maple wood products showed increased levels of demethoxylation with an S/G/P ratio of 1.0/4.2/1.2 versus 1.0/1.0/0.1 from the GVL extracted lignin products. After 4 h of reacting lignin monomers, dimers and trimers were produced with both the maple wood and extracted lignin. However, the 4 h maple wood products yielded twice the amount of lignin monomers (43.1%) as compared to the 4 h GVL extracted lignin products (20.1%). The GVL extracted lignin products were in the dimer to trimer molecular weight (MW, similar to 180-750 Da) ranges whereas the maple wood products were in the monomer to dimer MW ranges (similar to 94-500 Da) according to the GPC results. NMR and FT-ICR MS analyses show that both the 4 h maple wood products and 4 h GVL extracted lignin products undergo a high degree of hydrodeoxygenation, saturation, and repolymerization by C-C bond formation. The higher yield of lignin monomers from the maple wood is likely due to the lower lignin concentration that occurs during the reaction whereas higher lignin concentration during the reaction leads to more oligomerization reactions.

Computed Properties of C10H12O3. About 4-Methoxybenzyl acetate, If you have any questions, you can contact McClelland, DJ; Galebach, PH; Motagamwala, AH; Wittrig, AM; Karlen, SD; Buchanan, JS; Dumesic, JA; Huber, GW or concate me.

Reference:
Thiomorpholine – Wikipedia,
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Authors Das, S; Bhowmik, A; Sarkar, W; Mishra, A; Deb, I in AMER CHEMICAL SOC published article about in [Das, Sumit; Bhowmik, Arup; Sarkar, Writhabrata; Mishra, Aniket; Deb, Indubhusan] CSIR Indian Inst Chem Biol, Organ & Med Chem Div, Kolkata 700032, India; [Das, Sumit] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, Uttar Pradesh, India in 2021, Cited 75. Recommanded Product: 90-44-8. The Name is Anthrone. Through research, I have a further understanding and discovery of 90-44-8

Activation of anthrone via benzylic deprotonation in the presence of triethylamine paves the way for the 1,2-addition reaction with imines to provide the desired functionalized anthrones in good to excellent yields under mild and operationally simple reaction conditions with a broad range of substrate scopes without using any external additives or toxic stoichiometric reagents.

About Anthrone, If you have any questions, you can contact Das, S; Bhowmik, A; Sarkar, W; Mishra, A; Deb, I or concate me.. Recommanded Product: 90-44-8

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Thiomorpholine – Wikipedia,
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Jalili, Z; Tayebee, R; Zonoz, FM in [Jalili, Zahra; Tayebee, Reza; Zonoz, Farrokhzad M.] Hakim Sabzevari Univ, Sch Sci, Dept Chem, Sabzevar 9617976487, Iran published Eco-friendly synthesis of chromeno[4,3-b]chromenes with a new photosensitized WO3/ZnO@NH2-EY nanocatalyst in 2021.0, Cited 83.0. Computed Properties of C7H5NO3. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6.

A new heterogeneous photoredox nanocatalyst WO3/ZnO@NH2-EY (EY: eosin Y) was fabricated and characterized employing some instrumental techniques such as XRD, FT-IR, ICP, TGA, and SEM. The photocatalytic efficiency of the prepared material was investigated in the preparation of various chromeno[4,3-b]chromenes via a simple and practical method. The chromene derivatives were prepared through the condensation of aromatic aldehydes, dimedone, and coumarin under an open-air atmosphere in the presence of a green LED under solventless conditions. The significant advantages of this new method include low reaction time, easy work-up, cost-effective, wide substrate scope, excellent yield, and complete atom economy of the final products. Moreover, the prepared photocatalyst could be frequently recovered up to four times with only a little decrease in the catalytic activity. Furthermore, the progress of the condensation reaction is demonstrated to occur via a radical mechanism, which shows that reactive species such as O-2(-) and OH together with h(+) would be involved in the photocatalytic process. Stability and reusability studies also warranty good reproducibility of the nanocatalyst for at least 4 runs. Eventually, a hot filtration test ensured that the nanohybrid catalyst is stable in the reaction medium and its catalytic activity originates from the whole undecomposed conjugated composite.

Computed Properties of C7H5NO3. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Jalili, Z; Tayebee, R; Zonoz, FM or concate me.

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Thiomorpholine – Wikipedia,
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Product Details of 119-61-9. In 2021.0 CHEM-EUR J published article about C-C; DERIVATIVES; BOROLE; ANTIAROMATICITY; REDUCTION; ACTIVATION; COMPLEXES; ZIRCONIUM; SYSTEMS in [Zhu, Dezhao; Guo, Lulu; Li, Jianfeng; Cui, Chunming] Nankai Univ, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China; [Zhu, Dezhao; Guo, Lulu; Li, Jianfeng; Cui, Chunming] Nankai Univ, Coll Chem, Tianjin 300071, Peoples R China in 2021.0, Cited 62.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9.

The synthesis of benzoborole dianions by alkali metal reduction of BN-naphthalene derivatives via a ring-contraction strategy has been developed. Reduction of 1-alkynyl 2,1-benzazaborine 1 a in Et2O led to the elimination of alkynyllithium with the formation of 1-amino-1-benzoborole trilithium salt 2 a, whereas reduction of 1-phenyl 2,1-benzazaborine 1 c in THF yielded 1-phenyl-1-benzoborole dilithium salt 2 c with the elimination of ArNHLi. The trilithium and dilithium salts 2 a and 2 c have been fully characterized. Treatment of trilithium salt 2 a with Et3NHCl led to the selective protonation of the amino lithium to afford the dilithium salt 2 aH, which could be cleanly oxidized to 1-amino-1-benzoborole 3 in an excellent yield. Reaction of 1-phenyl-1-benzoborole dilithium salt 2 c with MeI yielded the lithium borate 4 c, which is luminescent both in solution and in the solid state.

About Benzophenone, If you have any questions, you can contact Zhu, DZ; Guo, LL; Li, JF; Cui, CM or concate me.. Product Details of 119-61-9

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

Product Details of 119-61-9. Authors Das, P; Ganguly, S; Margel, S; Gedanken, A in AMER CHEMICAL SOC published article about in [Das, Poushali; Ganguly, Sayan; Margel, Shlomo; Gedanken, Aharon] Bar Ilan Univ, Bar Ilan Inst Nanotechnol & Adv Mat BINA, Dept Chem, IL-5290002 Ramat Gan, Israel in 2021.0, Cited 69.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

This work presents the facile synthesis of heteroatom-doped fluorescent carbon quantum dots (C-dots), which could serve as an antioxidant. Herein, nitrogen, phosphorous, and sulfur codoped carbon dots (NPSC-dots) have been synthesized by a single-step hydrothermal strategy. Owing to the radical scavenging activity of the NPSC-dots, they were tested against several methods as well as in practical applications. The antioxidant ability of the NPSC-dots was efficiently utilized on plastic films by coating with these NPSC-dots. For the very first time, NPSC-dots were immobilized onto nonpolar plastic films (polypropylene) via photochemical covalent grafting to extend the shelf life of food items or storage without affecting the quality of plastic films. The NPSC-dot-coated PP film with negligible deterioration of transparency was extensively studied using scanning electron microscopy (SEM), atomic force microscopy (AFM), Fourier transform infrared (FTIR) analysis, X-ray photoelectron spectroscopy (XPS), contact angle measurement, and thermogravimetric analysis (TGA). The fluorescent character, antioxidant ability, and durability under different solvent systems of the coated film were examined. Also, the coated films were extensively and rigorously evaluated against simulated drastic environmental conditions to ensure the durability and antifogging application.

Product Details of 119-61-9. About Benzophenone, If you have any questions, you can contact Das, P; Ganguly, S; Margel, S; Gedanken, A or concate me.

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

Authors Li, CM; Zhang, FR; Shen, ZL in GEORG THIEME VERLAG KG published article about in [Li, Chunmei; Zhang, Furen] Shaoxing Univ, Sch Chem & Chem Engn, Zhejiang Key Lab Alternat Technol Fine Chem Proc, Shaoxing 312000, Zhejiang, Peoples R China; [Li, Chunmei; Shen, Zhenlu] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310032, Peoples R China in 2021, Cited 43. Category: thiomorpholine. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

A three-component domino reaction for the synthesis of naphtho[2,3-b][1,6]naphthyridine derivatives has been established. Such strategy exhibited excellent substrate scope including various enaminones and aldehydes that afforded a series of multifunctionalized naphtho[2,3-b][1,6]naphthyridine derivatives with 70-86% yields. The advantages of bond-forming efficiency, accessibility of starting materials, and water as sole byproducts provide invaluable access to biological 1,6-naphthyridines.

About 3-Nitrobenzaldehyde, If you have any questions, you can contact Li, CM; Zhang, FR; Shen, ZL or concate me.. Category: thiomorpholine

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

HPLC of Formula: C13H10O. Authors Hoque, ME; Hassan, MMM; Chattopadhyay, B in AMER CHEMICAL SOC published article about in [Hoque, Md Emdadul; Hassan, Mirja Md Mahamudul; Chattopadhyay, Buddhadeb] SGPGIMS Campus, Div Mol Synth & Drug Discovery, Ctr Biomed Res, Lucknow 226014, Uttar Pradesh, India in 2021, Cited 102. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

Here we describe the discovery of a new class of C-H borylation catalysts and their use for regioselective C-H borylation of aromatic, heteroaromatic, and aliphatic systems. The new catalysts have Ir-C(thienyl) or Ir-C(furyl) anionic ligands instead of the diamine-type neutral chelating ligands used in the standard C-H borylation conditions. It is reported that the employment of these newly discovered catalysts show excellent reactivity and ortho-selectivity for diverse classes of aromatic substrates with high isolated yields. Moreover, the catalysts proved to be efficient for a wide number of aliphatic substrates for selective C(sp(3))-H bond borylations. Heterocyclic molecules are selectively borylated using the inherently elevated reactivity of the C-H bonds. A number of late-stage C-H functionalization have been described using the same catalysts. Furthermore, we show that one of the catalysts could be used even in open air for the C(sp(2))-H and C(sp(3))-H borylations enabling the method more general. Preliminary mechanistic studies suggest that the active catalytic intermediate is the Ir(bis)boryl complex, and the attached ligand acts as bidentate ligand. Collectively, this study underlines the discovery of new class of C-H borylation catalysts that should find wide application in the context of C-H functionalization chemistry.

HPLC of Formula: C13H10O. About Benzophenone, If you have any questions, you can contact Hoque, ME; Hassan, MMM; Chattopadhyay, B or concate me.

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

Application In Synthesis of Benzophenone. Authors Prusty, N; Kinthada, LK; Meena, R; Chebolu, R; Ravikumar, PC in ROYAL SOC CHEMISTRY published article about in [Prusty, Namrata; Kinthada, Lakshmana K.; Meena, Rohit; Chebolu, Rajesh; Ravikumar, Ponneri Chandrababu] Natl Inst Sci Educ & Res NISER HBNI, Sch Chem Sci, Bhubaneswar 752050, Odisha, India in 2021.0, Cited 56.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

Bismuth(iii)-catalyzed regioselective functionalization at the C-6 position of tetrahydroquinolines and the C-5 position of indolines has been demonstrated. For the first time, one pot symmetrical and unsymmetrical arylation of isatins with tetrahydroquinolines was accomplished giving a completely new product skeleton in good to excellent yields. Most importantly, this protocol leads to the formation of a highly strained quaternary carbon stereogenic center, which is a challenging task. Benzhydryl and 1-phenylethyl trichloroacetimidates have been used as the alkylating partners to functionalize the C-6 and C-5 positions of tetrahydroquinolines and indolines, respectively. The scope of the developed methodology has been extended for the synthesis of the bioactive CYP19-inhibitor and its analogue.

Application In Synthesis of Benzophenone. About Benzophenone, If you have any questions, you can contact Prusty, N; Kinthada, LK; Meena, R; Chebolu, R; Ravikumar, PC or concate me.

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

An article Synthesis of Cinchona Urea Polymers and Their Evaluation as Catalyst in the Asymmetric Reactions WOS:000542426900009 published article about QUATERNARY AMMONIUM POLYMERS; MICHAEL ADDITION; CHIRAL POLYMERS; ORGANOCATALYSTS; ARYL in [Abdelkawy, Mahmoud A.; Itsuno, Shinichi] Toyohashi Univ Technol, Dept Appl Chem & Life Sci, Toyohashi, Aichi 4418580, Japan; [Abdelkawy, Mahmoud A.; Aly, El-Saied A.; El-Badawi, Mahmoud A.] Tanta Univ, Fac Sci, Chem Dept, Tanta 31527, Egypt in 2020, Cited 25. The Name is Anthrone. Through research, I have a further understanding and discovery of 90-44-8. Recommanded Product: 90-44-8

Chiral polyureas of cinchona alkaloids were synthesized via repetitive Mizoroki-Heck (MH) coupling reaction. The Pd-catalyzed polycondensation of cinchona urea dimers6and aromatic diiodide7afforded the chiral polyureas (P1-P4). The catalytic activity of the chiral polymers was subsequently investigated. The asymmetric Michael addition of ketoesters to nitroolefins was successfully catalyzed by the polymeric organocatalysts (P1-P4) to give the corresponding Michael adducts with high catalytic activities and excellent enantionselectivities (up to >99% ee). The polymeric catalysts were insoluble in commonly used organic solvents. They were easily recovered and reused several times without any loss of the catalytic activity.

Recommanded Product: 90-44-8. About Anthrone, If you have any questions, you can contact Abdelkawy, MA; Aly, EA; El-Badawi, MA; Itsuno, S or concate me.

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

Application In Synthesis of 3-Nitrobenzaldehyde. Zhou, SY; Guan, JY; Li, ZQ; Zhang, QF; Zheng, JF; Li, SH; Zhang, SB 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 published Synthesis of Fluorinated Poly(phenyl-alkane)s of Intrinsic Microporosity by Regioselective Aldehyde (A(2)) + Aromatics (B-2) Friedel-Crafts Polycondensation in 2021.0, Cited 45.0. 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.

About 3-Nitrobenzaldehyde, If you have any questions, you can contact Zhou, SY; Guan, JY; Li, ZQ; Zhang, QF; Zheng, JF; Li, SH; Zhang, SB or concate me.. Application In Synthesis of 3-Nitrobenzaldehyde

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