Category: 104-10-9

An article Heteroditopic Macrobicyclic Molecular Vessels for Single Step Aerial Oxidative Transformation of Primary Alcohol Appended Cross Azobenzenes WOS:000649101400054 published article about AROMATIC AZO-COMPOUNDS; PALLADIUM-CATALYZED OXIDATION; HOST-GUEST CHEMISTRY; RECOGNITION; ANILINES; COMPLEXATION; HYDROGEN; BINDING in [Sarkar, Sayan; Sarkar, Piyali; Ghosh, Pradyut] Indian Assoc Cultivat Sci, Sch Chem Sci, Kolkata 700032, India in 2021.0, Cited 101.0. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9. Safety of 2-(4-Aminophenyl)ethanol

A series of oxy-ether tris-amino heteroditopic macrobicycles (L1-L4) with various cavity dimensions have been synthesized and explored for their Cu(II) catalyzed selective single step aerial oxidative cross-coupling of primary alcohol based anilines with several aromatic amines toward the formation of primary alcohol appended cross azobenzenes (POCABs). The beauty of this transformation is that the easily oxidizable benzyl/primary alcohol group remains unhampered during the course of this oxidation due to the protective oxy-ether pocket of this series of macrobicyclic vessels. Various dimensionalities of the molecular vessels have shown specific size complementary selection for substrates toward efficient syntheses of regioselective POCAB products. To establish the requirement of the three-dimensional cavity based additives, a particular catalytic reaction has been examined in the presence of macrobicycles (L2 and L3) versus macrocycles (MC1 and MC2) and tripodal acyclic (AC1 and AC2) analogous components, respectively. Subsequently, L1-L4 have been extensively utilized toward the syntheses of as many as 44 POCABs and are characterized by different spectroscopic techniques and single crystal X-ray diffraction studies.

About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Sarkar, S; Sarkar, P; Ghosh, P or concate me.. Safety of 2-(4-Aminophenyl)ethanol

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

I found the field of Chemistry very interesting. Saw the article An Improved Synthesis of the Triethylene Glycol-Substituted 4-(N-Methyl-N-Boc-Amino)Styrylpyridine published in 2020.0. Category: amides-buliding-blocks, Reprint Addresses Hou, WB; Li, YL (corresponding author), Peking Union Med Coll, Inst Radiat Med, Tianjin Key Lab Radiat Med & Mol Nucl Med, Tianjin 300192, Peoples R China.; Hou, WB; Li, YL (corresponding author), Chinese Acad Med Sci, Tianjin 300192, Peoples R China.; Li, YL (corresponding author), Tianjin Univ Tradit Chinese Med, Tianjin 301617, Peoples R China.. The CAS is 104-10-9. Through research, I have a further understanding and discovery of 2-(4-Aminophenyl)ethanol

An improved five-step synthesis of triethylene glycol-substituted 4-(N-methyl-N-Boc-amino)styrylpyridine (6) is described. Using cost-effective starting materials, the developed synthesis route was synthetic, efficient, and chromatographic purification-free. The key point of the work is the one-pot synthesis of tert-butyl methyl(4-vinylphenyl)carbamate through methylation and elimination in the NaH/THF system. The new synthesis route shows the potential to achieve scaled-up preparation of 6 in the future.

Category: amides-buliding-blocks. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Jia, JH; Wei, HQ; Duan, YQ; Ning, HX; Yu, J; Zhu, Y; Hou, WB; Li, YL or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

SDS of cas: 104-10-9. I found the field of Pharmacology & Pharmacy very interesting. Saw the article Studies towards the development of a PET radiotracer for imaging of the P2Y(1) receptors in the brain: synthesis, F-18-labeling and preliminary biological evaluation published in 2019.0, Reprint Addresses Moldovan, RP (corresponding author), Helmholtz Zentrum Dresden Rossendorf, Inst Radiopharmaceut Canc Res, Permoserstr 15, D-04318 Leipzig, Germany.. The CAS is 104-10-9. Through research, I have a further understanding and discovery of 2-(4-Aminophenyl)ethanol.

Purine nucleotides such as ATP and ADP are important extracellular signaling molecules in almost all tissues activating various subtypes of purinoreceptors. In the brain, the P2Y(1) receptor (P2Y(1)R) subtype mediates trophic functions like differentiation and proliferation, and modulates fast synaptic transmission, both suggested to be affected in diseases of the central nervous system. Research on P2Y(1)R is limited because suitable brain-penetrating P2Y(1)R-selective tracers are not yet available. Here, we describe the first efforts to develop an F-18-labeled PET tracer based on the structure of the highly affine and selective, non-nucleotidic P2Y(1)R allosteric modulator 1-(2-[2-(tert-butyl)phenoxy]pyridin-3-yl)-3-[4- (trifluoromethoxy)phenyl]urea (7). A small series of fluorinated compounds was developed by systematic modification of the p-(trifluoromethoxy)phenyl, the urea and the 2-pyridyl subunits of the lead compound 7. Additionally, the p-(trifluoromethoxy)phenyl subunit was substituted by carborane, a boron-rich cluster with potential applicability in boron neutron capture therapy (BNCT). By functional assays, the new fluorinated derivative 1-{2-[2-(tert-butyl)phenoxy]pyridin-3-yl}-3-[4-(2-fluoroethyl) phenyl]urea (18) was identified with a high P2Y(1)R antagonistic potency (IC50 = 10 nM). Compound [F-18] 18 was radiosynthesized by using tetra-n-butyl ammonium [F-18]fluoride with high radiochemical purity, radiochemical yield and molar activities. Investigation of brain homogenates using hydrophilic interaction chromatography (HILIC) revealed [F-18]fluoride as major radiometabolite. Although [F-18]18 showed fast in vivo metabolization, the high potency and unique allosteric binding mode makes this class of compounds interesting for further optimizations and investigation of the theranostic potential as PET tracer and BNCT agent. (C) 2019 Elsevier Masson SAS. All rights reserved.

SDS of cas: 104-10-9. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Moldovan, RP; Wenzel, B; Teodoro, R; Neumann, W; Dukic-Stefanovic, S; Kraus, W; Rong, PJ; Deuther-Conrad, W; Hey-Hawkins, E; Krugel, U; Brust, P or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

In 2021.0 J ORG CHEM published article about AROMATIC AZO-COMPOUNDS; PALLADIUM-CATALYZED OXIDATION; HOST-GUEST CHEMISTRY; RECOGNITION; ANILINES; COMPLEXATION; HYDROGEN; BINDING in [Sarkar, Sayan; Sarkar, Piyali; Ghosh, Pradyut] Indian Assoc Cultivat Sci, Sch Chem Sci, Kolkata 700032, India in 2021.0, Cited 101.0. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9. Product Details of 104-10-9

A series of oxy-ether tris-amino heteroditopic macrobicycles (L1-L4) with various cavity dimensions have been synthesized and explored for their Cu(II) catalyzed selective single step aerial oxidative cross-coupling of primary alcohol based anilines with several aromatic amines toward the formation of primary alcohol appended cross azobenzenes (POCABs). The beauty of this transformation is that the easily oxidizable benzyl/primary alcohol group remains unhampered during the course of this oxidation due to the protective oxy-ether pocket of this series of macrobicyclic vessels. Various dimensionalities of the molecular vessels have shown specific size complementary selection for substrates toward efficient syntheses of regioselective POCAB products. To establish the requirement of the three-dimensional cavity based additives, a particular catalytic reaction has been examined in the presence of macrobicycles (L2 and L3) versus macrocycles (MC1 and MC2) and tripodal acyclic (AC1 and AC2) analogous components, respectively. Subsequently, L1-L4 have been extensively utilized toward the syntheses of as many as 44 POCABs and are characterized by different spectroscopic techniques and single crystal X-ray diffraction studies.

Product Details of 104-10-9. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Sarkar, S; Sarkar, P; Ghosh, P or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

An article Selective N-monomethylation of primary anilines with the controllable installation of N-CH2D, N-CHD2, and N-CD3 units WOS:000546177200004 published article about GENERAL CATALYTIC METHYLATION; CARBON-DIOXIDE; AROMATIC-AMINES; BORROWING HYDROGEN; DIMETHYL CARBONATE; REDUCTIVE METHYLATION; DEUTERATED DRUGS; COMPLEX BEARING; FORMIC-ACID; METHANOL in [Meng, Jing; Wang, Zhijuan] Nanjing Nch Univ, Sch Chem & Mol Engn, Inst Adv Synth, Nanjing 211816, Peoples R China; [Xia, Hui-Min; Xu, Ai-Qing; Wang, Yi-Feng; Zhang, Feng-Lian] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China; [Xia, Hui-Min; Xu, Ai-Qing; Wang, Yi-Feng; Zhang, Feng-Lian] Univ Sci & Technol China, Dept Chem, Hefei 230026, Peoples R China in 2020.0, Cited 81.0. HPLC of Formula: C8H11NO. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9

The selective N-monomethylation of primary anilines was realized by the use of the Me3N-BH3/N,N-dimethylformamide (DMF) system as the methyl source. This method also allows for the controllable introduction of N-CH2D, N-CHD2, and N-CD3 units with high levels of deuterium incorporation using Me3N-BH3/d(7)-DMF, Me3N-BD3/DMF and Me3N-BD3/d(7)-DMF systems, respectively.

About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Meng, J; Xia, HM; Xu, AQ; Wang, YF; Wang, ZJ; Zhang, FL or concate me.. HPLC of Formula: C8H11NO

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

An article Studies towards the development of a PET radiotracer for imaging of the P2Y(1) receptors in the brain: synthesis, F-18-labeling and preliminary biological evaluation WOS:000459358600012 published article about BINDING-SITES; P2X RECEPTORS; PURINERGIC RECEPTORS; DRUG-METABOLISM; P2Y1 RECEPTOR; IN-VIVO; ANTAGONISTS; DISCOVERY; LIGAND; RAT in [Moldovan, Rares-Petru; Wenzel, Barbara; Teodoro, Rodrigo; Dukic-Stefanovic, Sladjana; Deuther-Conrad, Winnie; Brust, Peter] Helmholtz Zentrum Dresden Rossendorf, Inst Radiopharmaceut Canc Res, Permoserstr 15, D-04318 Leipzig, Germany; [Kraus, Werner] BAM Fed Inst Mat Res & Testing, Richard Willstatter Str 11, D-12489 Berlin, Germany; [Neumann, Wilma; Hey-Hawkins, Evamarie] Univ Leipzig, Fac Chem & Mineral, Inst Inorgan Chem, D-04103 Leipzig, Germany; [Kruegel, Ute] Univ Leipzig, Fac Med, Rudolf Boehm Inst Pharmacol & Toxicol, D-04107 Leipzig, Germany; [Rong, Peijing] China Acad Chinese Med Sci, Inst Acupuncture & Moxibust, Beijing 100700, Peoples R China in 2019.0, Cited 67.0. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9. Recommanded Product: 104-10-9

Purine nucleotides such as ATP and ADP are important extracellular signaling molecules in almost all tissues activating various subtypes of purinoreceptors. In the brain, the P2Y(1) receptor (P2Y(1)R) subtype mediates trophic functions like differentiation and proliferation, and modulates fast synaptic transmission, both suggested to be affected in diseases of the central nervous system. Research on P2Y(1)R is limited because suitable brain-penetrating P2Y(1)R-selective tracers are not yet available. Here, we describe the first efforts to develop an F-18-labeled PET tracer based on the structure of the highly affine and selective, non-nucleotidic P2Y(1)R allosteric modulator 1-(2-[2-(tert-butyl)phenoxy]pyridin-3-yl)-3-[4- (trifluoromethoxy)phenyl]urea (7). A small series of fluorinated compounds was developed by systematic modification of the p-(trifluoromethoxy)phenyl, the urea and the 2-pyridyl subunits of the lead compound 7. Additionally, the p-(trifluoromethoxy)phenyl subunit was substituted by carborane, a boron-rich cluster with potential applicability in boron neutron capture therapy (BNCT). By functional assays, the new fluorinated derivative 1-{2-[2-(tert-butyl)phenoxy]pyridin-3-yl}-3-[4-(2-fluoroethyl) phenyl]urea (18) was identified with a high P2Y(1)R antagonistic potency (IC50 = 10 nM). Compound [F-18] 18 was radiosynthesized by using tetra-n-butyl ammonium [F-18]fluoride with high radiochemical purity, radiochemical yield and molar activities. Investigation of brain homogenates using hydrophilic interaction chromatography (HILIC) revealed [F-18]fluoride as major radiometabolite. Although [F-18]18 showed fast in vivo metabolization, the high potency and unique allosteric binding mode makes this class of compounds interesting for further optimizations and investigation of the theranostic potential as PET tracer and BNCT agent. (C) 2019 Elsevier Masson SAS. All rights reserved.

Recommanded Product: 104-10-9. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Moldovan, RP; Wenzel, B; Teodoro, R; Neumann, W; Dukic-Stefanovic, S; Kraus, W; Rong, PJ; Deuther-Conrad, W; Hey-Hawkins, E; Krugel, U; Brust, P or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

Authors Liu, B; Liu, CY; De Luca, HG; Pillai, SKR; Anthony, DB; Li, JH; Bismarck, A; Shaffer, MSP; Chan-Park, MB in ROYAL SOC CHEMISTRY published article about POLYIMIDE; NANOCOMPOSITES; STRENGTH; EPOXY in [Liu, Bo; Liu, Chengyin; Pillai, Suresh Kumar Raman; Li, Jianghua; Chan-Park, Mary B.] Nanyang Technol Univ, Sch Chem & Biomed Engn, 62 Nanyang Dr, Singapore 637459, Singapore; [De Luca, Hugo G.; Shaffer, Milo S. P.] Imperial Coll London, Dept Mat, London, England; [Anthony, David B.] Imperial Coll London, Dept Chem Engn, London, England; [Bismarck, Alexander] Univ Vienna, Facil Chem, Vienna, Austria; [Shaffer, Milo S. P.] Imperial Coll London, Dept Chem, London, England in 2019.0, Cited 27.0. Recommanded Product: 2-(4-Aminophenyl)ethanol. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9

Polyimides (PI) generally have a high affinity for single-walled carbon nanotubes (SWNTs), but they suffer from poor solubility in most low boiling point organic solvents and low compatibility with common resins (such as epoxy) used in composites, limiting their suitability as dispersants. PI block copolymer systems containing reactive poly(ester carbonate) s have not yet been reported and are expected to act as effective reactive dispersing agents of SWNTs. Herein, PI-derived block copolymers are synthesized via ring-opening copolymerization of lactide (LA) (a control monomer) and allyl-bearing 2-methyl-2-(allyloxycarbonyl)-propylene carbonate (MAC) from the OH-terminal ends of the PI block to produce PLA-PI-PLA (TB1, a control) and PMAC-PI-PMAC (TB2). The allyl pendant group of TB2 allows further facile functionalization to form a third series of epoxidized (EP) derivatives, i.e. PMACEP-block-PI-block-PMACEP (TB3). TB3 copolymer when mixed with a conventional structural epoxy resin forms blends that do not show inferior tensile properties compared with the epoxy, which is unusual. Furthermore, the mixing solvent tetrahydrofuran (THF) can be readily evaporated off after forming the blends. TB3-dispersed (2 wt%) SWNTs added to epoxy increased the tensile strength, modulus, and elongation at break of the resulting nanocomposite films by 40%, 34%, and 26% respectively, compared to the baseline epoxy resin. Furthermore, when TB3b triblock-dispersed SWNTs in epoxy were combined with fuzzy carbon fibers, i.e. carbon nanotube-grafted-carbon fibers (CNT-g-CF), a synergistic interfacial strength reinforcement was observed, together with shifting of the failure mode from the matrix interphase to the carbon fiber-grafted nanotube interface. The ultimate interfacial shear strength between the TB3-dispersed SWNT-epoxy matrix and the fuzzy carbon fibers (i.e., fibers having carbon nanotubes grown on them) measured via single fiber pull-out tests was 100 MPa, which was ca. 11% improvement over the baseline unsized carbon fiber in neat epoxy. To our knowledge, this is the first evidence of a synergistic enhancement in interfacial properties when fuzzy carbon fibers are combined with a SWNT-reinforced epoxy using the new epoxidized TB3 nanotube dispersing agent that forms a strong covalent TB3-epoxy interface. The new functionalizable TB3 synthesis route introduced here is generalizable to other PI-based copolymers with diverse functionalities and solvent compatibilities.

About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Liu, B; Liu, CY; De Luca, HG; Pillai, SKR; Anthony, DB; Li, JH; Bismarck, A; Shaffer, MSP; Chan-Park, MB or concate me.. Recommanded Product: 2-(4-Aminophenyl)ethanol

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

An article Efficient synthesis of cyclic amidine-based fluorophores via 6 pi-electrocyclic ring closure WOS:000525512500017 published article about ONE-POT SYNTHESIS; FLUORESCENT-PROBES; SULFONYL; REARRANGEMENT; TACHYKININ; ALKYNES; ACCESS; FUNCTIONALIZATION; 1,2,3-TRIAZOLES; ANNULATION in [Li, Guofeng; Zhao, Man; Yao, Ying; Xu, Jiecheng; Xue, Jianzhong; Hu, Tao; Li, Min; Hong, Liang] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangdong Key Lab Chiral Mol & Drug Discovery, Guangzhou 510006, Peoples R China; [Xie, Junqiu; Mou, Lingyun; Zhang, Xiaowei; Guo, Xiaomin; Sun, Wangsheng; Zhang, Ming] Lanzhou Univ, Sch Basic Med Sci, Key Lab Preclin Study New Drugs Gansu Prov, Lanzhou 730000, Peoples R China; [Wang, Zheng] Peking Univ, Sch Chem Biol & Biotechnol, Guangdong Key Lab Nanomicro Mat Res, Shenzhen Grad Sch, Shenzhen 518055, Peoples R China in 2020, Cited 67. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9. Recommanded Product: 104-10-9

Novel 10 pi-electron cyclic amidines with excellent fluorescence properties were synthesized by a general and efficient 6 pi-electrocyclic ring closure of ketenimine and imine starting from N-sulfonyl triazoles and arylamines. The photophysical properties of cyclic amidine fluorophores have been studied in detail and have shown good properties of a large Stokes shift, pH insensitivity, low cytotoxicity and higher photostability, which have great potential for biological imaging. Furthermore, this novel fluorophore was successfully applied to the localization of the NK-1 receptor in living systems.

Recommanded Product: 104-10-9. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Li, GF; Zhao, M; Xie, JQ; Yao, Y; Mou, LY; Zhang, XW; Guo, XM; Sun, WS; Wang, Z; Xu, JC; Xue, JZ; Hu, T; Zhang, M; Li, M; Hong, L or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

Authors Shimazaki, Y; Wata, C; Hashimoto, T; Maruoka, K in WILEY-V C H VERLAG GMBH published article about HYPERVALENT IODINE REAGENTS; OXIDATIVE SPIROLACTONIZATION; SPIROCYCLIZATION; DIARYLAMINES; FLUORINATION; ANILINES; PHENOLS in [Shimazaki, Yuto; Maruoka, Keiji] Kyoto Univ, Grad Sch Sci, Dept Chem, Sakyo Ku, Kyoto 6068502, Japan; [Wata, Chisato; Hashimoto, Takuya] Chiba Univ, Chiba Iodine Resource Innovat Ctr, Inage Ku, 1-33 Yayoi, Chiba 2638522, Japan; [Wata, Chisato; Hashimoto, Takuya] Chiba Univ, Dept Chem, Grad Sch Sci, Inage Ku, 1-33 Yayoi, Chiba 2638522, Japan; [Maruoka, Keiji] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Panyu District, Peoples R China; [Maruoka, Keiji] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan in 2021.0, Cited 89.0. HPLC of Formula: C8H11NO. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9

We report herein the development of an enantioselective oxidative para-dearomatization of sulfonanilides with water by use of an indanol-based chiral organoiodine catalyst, originally developed in our group. This reaction proceeds efficiently by the use of N-mesyl-protected anilines as substrates, giving functionalized p-quinol imines in good yields and moderate to high enantioselectivities.

HPLC of Formula: C8H11NO. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Shimazaki, Y; Wata, C; Hashimoto, T; Maruoka, K or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

An article Photo-induced copper-mediated (meth)acrylate polymerization towards graphene oxide and reduced graphene oxide modification WOS:000552030700001 published article about TRANSFER RADICAL POLYMERIZATION; CARBON NANOTUBES; CLICK CHEMISTRY; DISPERSED GRAPHENE; ORGANIC-SYNTHESIS; VISIBLE-LIGHT; SURFACE; NANOCOMPOSITES; NANOPARTICLES; BRUSHES in [Railian, Svitlana; Maes, Lowie; Junkers, Tanja] UHasselt Inst Mat Res, Polymer React Design Grp, Agoralaan, B-3590 Diepenbeek, Belgium; [Haven, Joris J.; Junkers, Tanja] Monash Univ, Sch Chem, 19 Rainforest Walk, Clayton, Vic 3800, Australia; [De Sloovere, Dries; Van Bael, Marlies K.; Hardy, An] UHasselt Inst Mat Res, Inorgan & Phys Chem, Agoralaan, B-3590 Diepenbeek, Belgium; [De Sloovere, Dries; Van Bael, Marlies K.; Hardy, An] Energyville, Thor Pk 8320, B-3600 Genk, Belgium; [De Sloovere, Dries; Adriaensens, Peter; Van Bael, Marlies K.; Hardy, An; Deferme, Wim] IMEC Vzw Div IMOMEC, Wetenschapspk 1, B-3590 Diepenbeek, Belgium; [Trouillet, Vanessa] Karlsruhe Inst Technol KIT, Inst Appl Mat IAM, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany; [Trouillet, Vanessa; Welle, Alexander] Karlsruhe Inst Technol KIT, Karlsruhe Nano Micro Facil KNMF, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany; [Welle, Alexander] Karlsruhe Inst Technol KIT, Inst Funct Interfaces, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany; [Adriaensens, Peter] UHasselt Inst Mat Res, Nucl Magnet Resonance Spect Grp, Agoralaan, B-3590 Diepenbeek, Belgium; [Deferme, Wim] UHasselt Inst Mat Res, Wetenschapspk 1, B-3590 Diepenbeek, Belgium in 2020.0, Cited 84.0. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9. SDS of cas: 104-10-9

The preparation of well-dispersed graphene/polymer nanocomposites is challenging due to the poor miscibility of graphene sheets in a polymer matrix. To enhance the interaction between both phases, graphene sheets can be decorated with polymer chains. Herein, different strategies to graft poly(methyl methacrylate) (PMMA) and poly(di(ethylene glycol) ethyl ether acrylate) (PDEGA) chains at various positions on graphene oxide and reduced graphene oxide (GO/rGO) sheets are compared. Chain attachment was achieved by grafting-to and grafting-from methods. Grafting-to was performed by classical copper (I)-catalyzed alkyne azide cycloaddition. Using a grafting-from approach, PMMA and PDEGA brushes were grown from GO and rGO sheets via surface-initiated photo-induced copper-mediated polymerization (SI-photoCMP). SI-photoCMP is a robust and efficient method that allows polymerizations to be carried out under mild conditions and with reduced catalyst concentration. Moreover, the successful implementation of SI-photoCMP in a continuous-flow set-up enables easy upscaling of the system and is, therefore, a more efficient and environmentally friendly process for GO/rGO surface modification. By using the grafting-to approach, the grafting density of PMMA (M-n = 2,600 g/mol) was one chain per 990 carbons of graphene. In contrast, longer PMMA chains (M-n = 40,300 g/mol) and higher grafting density were obtained via the grafting-from method (one PMMA chain per 140 carbons of graphene).

SDS of cas: 104-10-9. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Railian, S; Haven, JJ; Maes, L; De Sloovere, D; Trouillet, V; Welle, A; Adriaensens, P; Van Bael, MK; Hardy, A; Deferme, W; Junkers, T or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics