Day: October 9, 2020

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.14024-18-1,Iron(III) acetylacetonate,as a common compound, the synthetic route is as follows.

The magnetic iron oxide oxide nanoparticles [Fe-nanoparticles] were prepared as described [64-66]. In brief, the iron oleate complex was synthesized from 2mmol iron(III)acetyl acetonate [Fe(acac)3] that was suspended in 20mL of benzyl ether. After addition of 10mmol 1,2-hexadecanediol, 6mmol oleic acid and finally 6mmol oleylamine the reaction was started under argon atmosphere and heated to 250C under reflux for 30min. The resulting dark-brown solution was cooled to room temperature; during this process the magnetite nanoparticles are produced; they have a size of ?7nm, are monodisperse, and can be conveniently attracted as well as translocated in the organic as well as the aqueous environment by using a circular magnet 18¡Á10mm.

14024-18-1, 14024-18-1 Iron(III) acetylacetonate 91759530, airon-catalyst compound, is more and more widely used in various fields.

Reference£º
Article; Li, Qiang; Wang, Xiaohong; Korzhev, Michael; Schroeder, Heinz C.; Link, Thorben; Tahir, Muhammad Nawaz; Diehl-Seifert, Baerbel; Mueller, Werner E.G.; Biochimica et Biophysica Acta – General Subjects; vol. 1850; 1; (2015); p. 118 – 128;,
Iron Catalysis in Organic Synthesis | Chemical Reviews
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.1271-51-8,Vinylferrocene,as a common compound, the synthetic route is as follows.

General procedure: A stirred mixture of bromo compound (1.0 equiv.), Pd(OAc)2 (0.1/0.2 equiv.) in dry DMF (25mL) under nitrogen was successively treatedwith K2CO3 (3.0/6.0 equiv.) and tetrabutylammoniumbromide (0.1/0.2equiv.)and stirred for 30 min. The vinyl dendron (1.0/2.0 equiv.)wasthen added and the resulting mixture was stirred at 90 ¡ãC for 12 h,cooled and filtered. The filtrate was evaporated to dryness in vacuo.The residue was extracted with CHCl3 (3 ¡Á 100 mL), washed withwater (3 ¡Á 100 mL) and dried over anhydrous Na2SO4. Evaporation ofthe organic layer afforded the crude product,whichwas purified by columnchromatography using the eluent as mentioned under each compoundto afford the corresponding conjugated dendrimers.

1271-51-8, The synthetic route of 1271-51-8 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Ravivarma, Mahalingam; Kumar, Kaliamurthy Ashok; Rajakumar, Perumal; Pandurangan, Arumugam; Journal of Molecular Liquids; vol. 265; (2018); p. 717 – 726;,
Iron Catalysis in Organic Synthesis | Chemical Reviews
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

14024-18-1, Iron(III) acetylacetonate is a iron-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: A solvothermal method was implemented to prepare CuFe2O4and Fe3O4 NPs. For the synthesis of Fe3O4 NPs, 4 mmol of Fe(acac)3 and 40 ml of triethylene glycol were mixed in a 200 ml round bottom flask connected to a reflux condenser. To homogenize thesolution, the temperature was increased to 100 C and maintainedat this temperature for 1 h. Afterwards the obtained homogenoussolutionwas transferred to a Teflon lined autoclave (75 ml capacity)and then placed in a furnace at 260 C for 24 h. Next, the mixturewas left to cool down to room temperature, which resulted in a black homogeneous dispersion containing magnetite nanoparticles.The obtained product was washed with acetone severaltimes using centrifugation. Then, the nanoparticles were put to dryin an oven at 50 C for 12 h. For the synthesis of CuFe2O4 NPs, thesame procedure was employed except that the stoichiometricamount of Cu(acac)2 was added to the triethylene glycol at the firstof synthesis process. Briefly, the synthesis process is schematicallyshown in Fig. 1.

14024-18-1, As the paragraph descriping shows that 14024-18-1 is playing an increasingly important role.

Reference£º
Article; Fotukian, Seyedeh Maryam; Barati, Aboulfazl; Soleymani, Meysam; Alizadeh, Ali Mohammad; Journal of Alloys and Compounds; vol. 816; (2020);,
Iron Catalysis in Organic Synthesis | Chemical Reviews
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

1271-55-2, Acetylferrocene is a iron-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

A solution of pure TsNHNH2 (15 mmol) in methanol (30 mL) was stirred and heated to 60 C until the TsNHNH2 dissolved. The mixture was cooled to room temperature. Then a solution of acetyl ferrocene 1a (10 mmol) in methanol was dropped into the mixture slowly. After approximately 0.5 h, the crude products could be obtained as solid precipitate. The precipitate was washed with petroleum ether then removed in vacuo to give yellow solid 2a in 86 % yield. mp 187-189 C. 1H NMR (500 MHz, DMSO) delta 10.00 (s,1H), 7.81 (d, J = 7.9 Hz, 2H), 7.43 (d, J = 7.8 Hz, 2H), 4.49 (s, 2H), 4.29 (s, 2H), 3.93 (s, 5H), 2.36 (s, 3H), 2.04 (s, 3H). 13C NMR (126 MHz, DMSO) d 155.1, 143.0, 136.4, 129.1, 127.6, 69.6, 68.9, 66.8, 20.9, 15.0. HRMS (ESI-TOF) m/z: [M]+ calcd. for C19H20FeN2O2S 396.0595; Found: 396.0594.

1271-55-2, As the paragraph descriping shows that 1271-55-2 is playing an increasingly important role.

Reference£º
Article; Ling, Li; Hu, Jianfeng; Zhang, Hao; Tetrahedron; vol. 75; 17; (2019); p. 2472 – 2481;,
Iron Catalysis in Organic Synthesis | Chemical Reviews
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.1271-42-7,Ferrocenecarboxylic acid,as a common compound, the synthetic route is as follows.

Compound 15 was reacted with tert-butoxide, t-BuLi and 002 yielding compound 3a. The synthesis of ferrocenecarboxylic acid 3a (step a) was adapted from a procedure from Witte et al. (Organometallics 1999, 18, 4147). Compound 3a was reacted with oxalyl chloride under reflux yielding compound 3b. The synthesis of chlorocarbonyl ferrocene 3b (step b) was adapted from a procedure of Cormode et al. (Dalton Trans.201 0, 39, 6532). Optionally anadapted procedure of Lorkowski et. al. (VIII. Preparation of monomeric and polymeric ferrocenylene oxadiazoles, J. Prakt. Chem. 1967, 35, 149-58) may be applied. Chlorocarbonyl ferrocene 3b and 2-amino-2-hydroxymethylproprionitrile 6 were dissolved in dry THF and Triethylamine was added (step c). After evaporation of the solvent and purification by column chromatography N-(2-cyano-1-hydroxypropan-2-yl)ferroceneamide 7a was isolated in 29% yield according to an adapted procedure of Gasser et al. (J. Organomet.Chem. 2010, 695, 249-255). Compound 7a was reacted with one equivalent of 5a in thepresence of K2003 and 18-crown-6 in dry CH3CN according to an adapted procedure ofGasser et al. (J. Organomet. Chem. 2007, 692, 3835-3840) and Gasser et al. (J. Med.Chem. 2012, 55, 8790-8798), yielding compound 1 in a yield of 43%.

1271-42-7, 1271-42-7 Ferrocenecarboxylic acid 499634, airon-catalyst compound, is more and more widely used in various fields.

Reference£º
Patent; UNIVERSITAeT ZUeRICH; THE UNIVERSITY OF MELBOURNE; GASSER, Gilles; GASSER, Robin B.; HESS, Jeannine; JABBAR, Abdul; PATRA, Malay; WO2015/44396; (2015); A1;,
Iron Catalysis in Organic Synthesis | Chemical Reviews
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.1271-51-8,Vinylferrocene,as a common compound, the synthetic route is as follows.

General procedure: In an Schlenk tube under argon one of the following central coresC1, or C2 was mixed with 5percent palladium (II) acetate, Pd(OAc)2, 10percentTris(o-tolyl)phosphine, P(o-tol)3, and vinyl ferrocene, 1-Fc, in triethylamine/THF, 15 mL/15 mL. The resulting mixture was stirred and refluxedovernight. After removing the solvent under reduced pressure,the oil obtained was washed with distillated water and extracted inCH2Cl2 three times and dried over MgSO4. The extract was concentratedto dryness and purified by column chromatography (silica gel60) using hexane/CH2Cl2 2:1 (V/V) mixtures as eluent. The correspondingcompounds were isolated after removing the solvent in a rotaryevaporator. Compound 1. 1-Fc (187 mg, 8.84 mmol), C1 (150 mg,0.253 mmol), Pd(OAc)2 (2.8 mg, 0.0126 mmol), P(o-tol)3 (7.7 mg,0.0253 mmol), triethylamine/THF, 15 mL/15 mL. Yield 49.5percent. IR wavenumber(KBr): =1713 cm?1 (eC]O), 1590 cm?1 (eC]Ce). 1HNMR (CDCl3, 400 MHz): delta=4.10 (15H, pst, C5H5), 4.27 (6H,pst?C5H4), 4.44 (6H, s, ?C5H4), 6.68 (3H, d, J=16.0 Hz, ]CH), 6.89(3H, d, J=16.0 Hz, ]CH), 7.31 (6H, d, J=8.2 Hz, Harom), 7.50 (6H, d,J=8.4 Hz, Harom). 13C NMR (100.6 MHz, CDCl3): delta=67.05, 69.25,69.66, 82.76, 124.74, 126.48, 128.53, 128.60, 128.91, 131.70, 139.04.Analysis calculated for C57H45O3Fe3N3: C, 69.3; H, 4.59; N, 4.26.Found: C, 68.61; H, 4.12; N, 4.32. MP: 199 ¡ãC – 200 ¡ãC.

1271-51-8, As the paragraph descriping shows that 1271-51-8 is playing an increasingly important role.

Reference£º
Article; Santos, Juan C.; Madrid-Moline, Franco; Cisternas, Carlos A.; Paul, Frederic; Escobar, Carlos A.; Jara-Ulloa, Paola; Trujillo, Alexander; Inorganica Chimica Acta; vol. 486; (2019); p. 95 – 100;,
Iron Catalysis in Organic Synthesis | Chemical Reviews
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

1271-51-8, Vinylferrocene is a iron-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: A mixture of 4-bromo-7-(piperidin-1-yl)benzo[c][1,2,5]thiadiazole (2a) (0.298 g, 1 mmol), 4-vinylpyridine (0.115 g, 1.1 mmol), Pd(OAc)2 (5.0 mg, 0.022 mmol), NaOAc (0.82 g, 10 mmol), n-Bu4NBr (0.065 g, 0.2 mmol) and N,N-dimethylformamide (10 mL) was heated at 100 ¡ãC for 24 h under nitrogen atmosphere. After cooling, the reaction was quenched by adding excess water. The precipitate formed was filtered, washed with water, dissolved in dichloromethane, and dried over anhydrous sodium sulfate. After evaporation of the volatiles, the residue was purified by column chromatography on silica gel, using a hexanes/dichloromethane mixture (2:3) as eluant to obtain the title compound 3a. 4.2.6 4-((E)-2-Ferocenylvinyl)-7-((E)-2-(pyridin-4-yl)vinyl)benzo[c][1,2,5]thiadiazole (6c) Compound 6c (0.277 g, 73percent) was prepared as dark solid by following a procedure similar to that described above for 6a by using vinylferrocene. Rf (70percent CH2Cl2/hexanes) 0.39; mp 184-186 ¡ãC; numax (KBr film) 2924, 2847, 1622, 1380, 1100, 965, 810 cm-1; deltaH (500.13 MHz, CDCl3) 4.19 (5H, s, Cp), 4.40 (2H, s, Cp), 4.62 (2H, s, Cp), 7.22 (1H, s), 7.50 (2H, s), 7.61 (1H, buried d, vinyl), 7.69 (1H, d, J=6.0 Hz), 7.75 (1H, d, J=16.0 Hz, vinyl), 7.84 (1H, d, J=16.0 Hz, vinyl), 7.99 (1H, d, J=16.0 Hz, vinyl), 8.6 (2H, br s, pyridine); deltaC (125.77 MHz, CDCl3) 67.5, 69.5, 69.9, 83.0, 121.0, 121.5, 125.2, 126.8, 129.1, 129.2, 129.8, 131.2, 134.0, 145.0, 150.2, 153.7, 153.9; HRMS (ESI): MH+, found 449.0625. C25H19FeN3S requires 449.0649.

1271-51-8, 1271-51-8 Vinylferrocene 16211828, airon-catalyst compound, is more and more widely used in various fields.

Reference£º
Article; Prasad Bolisetty; Li, Chun-Ting; Thomas Justin; Bodedla, Govardhana Babu; Ho, Kuo-Chuan; Tetrahedron; vol. 71; 24; (2015); p. 4203 – 4212;,
Iron Catalysis in Organic Synthesis | Chemical Reviews
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

14024-18-1, Iron(III) acetylacetonate is a iron-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

One pot reaction was carried out by adding 2 mmol of metal precursor Fe (acac), 10 mmol of 1,2-hexadecanediol, 6 mmol of oleic acid and 6 mmol of oleylamine, 10 mmol of a solvent (benzyl ether 10 Ml). The mixture was heated to 200 degrees Celsius for 2 hours under nitrogen gas flow protection. Then, the obtained black mixture was cooled at room temperature. The mixture was precipitated by the addition of ethanol and separated via a centrifuge and dispersed in hexane with oleic acid (~ 0.05 mL) and oleylamine (~ 0.05 mL). The undispersed mixture was removed and again precipitated in ethanol. The precipitate was washed at least three times, and the washed precipitate was dried in vacuum at about 40 DEG C to seal the obtained iron oxide nanoparticles.

14024-18-1, The synthetic route of 14024-18-1 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; INDUSTRIAL COOPERATION FOUNDATION CHONBUK NATIONAL UNIVERSITY; Kim, Cheol-Sang; Park, Chan-Hee; Rajan Unnithan, Afeesh; Amin, GhavamiNejad; Arathyram, Ramachandra Kurup Sasikal; (29 pag.)KR2016/145991; (2016); A;,
Iron Catalysis in Organic Synthesis | Chemical Reviews
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

1271-51-8, Vinylferrocene is a iron-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

A deoxygenated mixture of vinylferrocene (170mg, 0.80mmol), K2CO3 (1.50g, 11mmol), tetrabutylammonium bromide (1.19g, 3.70mmol), 6-bromochromone-3-propionic acid (196.8mg, 0.66mmol) and Pd(OAc)2 (20mg, 0.09mmol) in DMF (23ml) was heated at 95¡ãC for 19h. After cooling to r. t. the reaction mixture was evaporated to dryness. Solid residue was dissolved in chloroform and extracted six times with water followed by extraction with 3.5percent HClaq. The organic phase was dried with MgSO4, filtered and the solvent was removed from the filtrate in vacuo. The residue was subjected to chromatography on SiO2 (eluent: CHCl3/methanol, 50:5). Finally the analytically pure products were obtained after recrystallization from DMSO/water.

1271-51-8, 1271-51-8 Vinylferrocene 16211828, airon-catalyst compound, is more and more widely used in various fields.

Reference£º
Article; Kowalski, Konrad; Koceva-Chy, Aneta; Szczupak, Lukasz; Hikisz, Pawel; Bernasin?ska, Joanna; Rajnisz, Aleksandra; Solecka, Jolanta; Therrien, Bruno; Journal of Organometallic Chemistry; vol. 741-742; 1; (2013); p. 153 – 161;,
Iron Catalysis in Organic Synthesis | Chemical Reviews
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion

1273-86-5, Ferrocenemethanol is a iron-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

In a Schlenk tube, 1.00 g (4.63 mmol) of ferrocenyl methanol and 0.47 mL(4.7 mmol) of 2,4 pentanedione were dissolved in 8 mL of acetonitrile at room temperature (rt). After 5 min of stirring, 0.125 g (0.23 mmol) of cerium(IV)ammonium nitrate (5% molar) were added. The reaction mixture was stirred for 30 min at rt and then evaporated under reduced pressure. The solid residue was mixed with 5 mL of water and extracted with 10 mL of dichloromethane.The organic phase was dried over MgSO4, filtered off and evaporated under reduced pressure to afford 1.25 g (4.29 mmol, 90% yield) of 1 as an orange oil.

1273-86-5, As the paragraph descriping shows that 1273-86-5 is playing an increasingly important role.

Reference£º
Article; Ahumada, Guillermo; Roisnel, Thierry; Hamon, Jean-Rene; Carrillo, David; Manzur, Carolina; Journal of the Chilean Chemical Society; vol. 58; 4; (2013); p. 1963 – 1966;,
Iron Catalysis in Organic Synthesis | Chemical Reviews
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion