Day: August 18, 2020

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.34946-82-2,Copper(II) trifluoromethanesulfonate,as a common compound, the synthetic route is as follows.

Tert-leucine phosphinoazomethinylate potassium salt (100 mg, 0.23 mmol, 1 eq.) and copper bis-triflate Cu(OTf)2 (114 mg, 0.23 mmol, 1 eq.) are placed in a round-bottom flask. Anhydrous THF is then added (9 mL, 40 mL per mmol). The reaction mixture is agitated at room temperature for 1 hour. The solvent is evaporated and the product is dried under reduced pressure. A green powder is obtained (210 mg, 98%).

The synthetic route of 34946-82-2 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Mauduit, Marc; Rix, Diane; Crevisy, Christophe; Wencel, Joanna; US2010/267956; (2010); A1;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

7787-70-4, Copper(I) bromide is a copper-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: The complexes were prepared according to the following method [14]: 1mmol of copper(I) bromide or copper(I) chloride is stirred in methanol until complete dissolution. Then, 2.1 mmol of the corresponding phosphine ligand was added. The mixture was stirred at 60C for 30min. under nitrogen atmosphere. A microcrystalline precipitate was obtained by concentration of the solution at reduced pressure. The solid product was dissolved in a dichloromethane/methanol mixture and the solution was gradually cooled to 4C to give an air stable and colorless crystalline solid suitable for X-ray single-crystal diffraction studies.

As the paragraph descriping shows that 7787-70-4 is playing an increasingly important role.

Reference£º
Article; Espinoza, Sully; Arce, Pablo; San-Martn, Enrique; Lemus, Luis; Costamagna, Juan; Faras, Liliana; Rossi, Miriam; Caruso, Francesco; Guerrero, Juan; Polyhedron; vol. 85; (2015); p. 405 – 411;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

6046-93-1, Copper(II) acetate hydrate is a copper-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: A solution of Cu(OAc)2¡¤H2O (4.6 mmol) in methanol (10 mL) was added to a solution of corresponding porphyrin (1.15 mmol) in methylene chloride (50 mL). The resulting mixture was stirred flor 1.5 h at room temperature with TLC monitoring (CHCl3-hexane 1:2). Then the reaction mixture was poured into water and extracted with methylene chloride. The organic layer was dried over Na2SO4, and the solvent was removed under reduced pressure. The residue was used without purification. 5,10,15,20-(tetraphenylporphyrinato)copper(II) (13) [56] (757 mg,yield 97%). UV-Vis (CH2Cl2) >max, (j10-3) nm: 414 (611), 539 (29).APCI-MS Found: [M]+ 676.16; ?C44H28CuN4? requires [M]+ 676.26.

As the paragraph descriping shows that 6046-93-1 is playing an increasingly important role.

Reference£º
Article; Ol’shevskaya, Valentina A.; Alpatova, Viktoriya M.; Radchenko, Alexandra S.; Ramonova, Alla A.; Petrova, Albina S.; Tatarskiy, Victor V.; Zaitsev, Andrei V.; Kononova, Elena G.; Ikonnikov, Nikolay S.; Kostyukov, Alexey A.; Egorov, Anton E.; Moisenovich, Mikhail M.; Kuzmin, Vladimir A.; Bragina, Natalya A.; Shtil, Alexander A.; Dyes and Pigments; vol. 171; (2019);,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

7787-70-4, Copper(I) bromide is a copper-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

Triethyl phosphite (183g, 1.1 mol) was added to a suspension of copper(I) bromide (164.5 g, 1.15 mol) in toluene (500 ml). The mixture was heated at 80C for 3 h with stirring, then left to cool and settle. The clear solution was decanted from the solid residue and the solvent evaporated on a rotary evaporator at 60C, to provide copper(I) bromide triethyl phosphite complex as a clear colourless oil, 336g (94% crude yield).

As the paragraph descriping shows that 7787-70-4 is playing an increasingly important role.

Reference£º
Patent; ASTRAZENECA AB; ASTRAZENECA UK LIMITED; WO2006/67416; (2006); A1;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.34946-82-2,Copper(II) trifluoromethanesulfonate,as a common compound, the synthetic route is as follows.

2-Phenylpyridine 1a (71 muL, 0.5 mmol),1,2-diphenylethylene 2a (89.7 mg, 0.5 mmol),{[Cp * RhCl2] 2} (3.1 mg, 1 mol%),AgOTf (5.1 mg, 0.02 mmol),Cu (OTf) 2 (180.8 mg, 0.5 mmol)Was added to 2.0 mL of methanol, under argon (1 atm)120 oC reaction after 22 hours to stop the reaction,Diatomaceous earth filter, dichloromethane washing, collecting organic phase evaporated solvent,Methanol / ether / petroleum ether (1: 4: 100) to give the pure isoquinoline salt derivative 3aa. The product was a white solid in 91%

The synthetic route of 34946-82-2 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences; Huang, Hanmin; Zhang, Guoyang; (21 pag.)CN104177357; (2017); B;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.7787-70-4,Copper(I) bromide,as a common compound, the synthetic route is as follows.

A yellow solution of 168.0 mg (0.736 mmol) of 2b in toluene (10 mL) was added to a green CH3CN solution (20 mL) containing 105.6 mg (0.736 mmol) CuBr with stirring at ambient temperature. The reaction mixture was allowed to stir overnight forming a dark green precipitate. The solution was filtered, and the precipitate washed with cold MeOH (5 mL) and dried under vacuum (57.9 mg, 17% yield). 1H and 13C{1H} NMR spectra could not be recorded due to strong paramagnetic properties of complex. FTIR (KBr) 3425, 3056, 3006, 2918, 1627, 1593, 1466, 1436, 1300, 1269, 1236, 1201, 1157, 1106, 1092, 1069, 1046, 967, 958, 914, 849, 774, 767, 744, 694, 652, 567, 543, 501, 458, 417 cm-1. Anal. Calc’d. for C13H12Br2CuN2S: C = 34.57%, H = 2.68%, N = 6.20%. Found: C = 34.17%, H = 3.36%, N = 6.44%. UV-vis (DMF, 0.050 mg/mL) lambdamax (epsilon) = 266 (7.6 * 103), 353.

The synthetic route of 7787-70-4 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Cross, Edward D.; Ang, M. Trisha C.; Richards, D. Douglas; Clemens, Amy C.; Muthukumar, Harshiny; McDonald, Robert; Woodfolk, London; Ckless, Karina; Bierenstiel, Matthias; Inorganica Chimica Acta; vol. 481; (2018); p. 69 – 78;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.7787-70-4,Copper(I) bromide,as a common compound, the synthetic route is as follows.

A mixture of CuBr (0.57g, 4mmol) and 2,9-dimethyl-1,10-phenanthroline (L3) (0.72g, 2mmol) in CH3CN (30ml) was stirred overnight under nitrogen atmosphere at room temperature. The copper complex was obtained as a brick-red solid in 90% yield.

As the paragraph descriping shows that 7787-70-4 is playing an increasingly important role.

Reference£º
Article; Liang, Zhaoli; Wang, Fei; Chen, Pinhong; Liu, Guosheng; Journal of Fluorine Chemistry; vol. 167; (2014); p. 55 – 60;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.578743-87-0,[1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper chloride,as a common compound, the synthetic route is as follows.

In a glove box, IPrCuCl (224 mg, 0.46 mmol) and potassium tris(1-pyrazolyl)borohydride (127 mg, 0.50 mmol) in THF in a 40 mixture was stirred at room temperature for 3 hours dongan. Filtered through a plug of Celite and the reaction mixture after the evaporation of the solvent under reduced pressure to give product as a white powder IPrCuTp

As the paragraph descriping shows that 578743-87-0 is playing an increasingly important role.

Reference£º
Patent; University Of Southern California; Thompson, Mark E; Hamz, Rasya; Durovitch, Peter I; (50 pag.)KR2015/26932; (2015); A;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.13395-16-9,Bis(acetylacetone)copper,as a common compound, the synthetic route is as follows.

General procedure: In a typical synthesis of Cu40Ag60, 0.45mmol Cu(acac)2 and 0.35 Ag (ac) was mixed with 3mL of OAm, 1 mL of OAc and 11mL of ODE. All synthesis was conducted in a four-necked glass reactor allowing the precise temperature control and inert gas atmosphere under dark conditions. Firstly, the mixture was heated to 60C and kept at this temperature for 10min. Then, the mixture was heated to 180C and kept at this temperature for 30min before it was cooled down to room temperature. After cooling, the resultant reaction mixture was collected with hexane (2mL) and the NPs were separated by centrifugation (8500rpm, 12min) after adding isopropanol (40mL). To further purify the yielded CuAg NPs, the product was centrifuged (8500rpm, 12min) one more time with ethanol (40mL). Finally, the remaining product was dispersed in hexane (10mL) for further use. By using the same recipe and varying metal precursor amounts, two different compositions of CuAg NPs were synthesized. Reductive mixing of 0.3mmol Cu(acac)2 and 0.5 Ag(ac) resulted in Cu30Ag70 NPs and mixing 0.6mmol Cu(acac)2 with 0.4 Ag (ac) led to Cu60Ag40. Synthesis of Ag NPs was conducted with the same recipe without using Cu precursor.

13395-16-9 Bis(acetylacetone)copper 2723615, acopper-catalyst compound, is more and more widely used in various.

Reference£º
Article; Balkan, Timucin; Kuecuekkececi, Hueseyin; Kaya, Sarp; Metin, Oender; Zarenezhad, Hamaneh; Journal of Alloys and Compounds; vol. 831; (2020);,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

578743-87-0, [1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper chloride is a copper-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

2-(2-Pyridyl)benzimidazole (78.1 mg, 0.4 mmol) was dissolved in 10 mL of dry THF under N2 and this solution was transferred via cannula to suspension of sodium hydride (17.6 mg, 0.44 mmol, 60% in mineral oil) in dry THF. Reaction mixture was stirred at RT for 1 h and then chloro[l,3-bis(2,6-di-i-propylphenyl)imidazol-2- ylidene]copper(I) (195.1 mg, 0.4 mmol) was added. Reaction mixture was stirred at RT for 3 h. The resulting mixture was filtered through Celite and solvent was removed by rotary evaporation. Recrystallization by vapor diffusion of Et20 into a CH2C12 solution of product gave 154 mg (59.5%>) of dark yellow crystals. Anal, calcd. for C39H44CuN5: C, 72.47; H, 6.86; N, 10.48; Found: C, 72.55; H, 6.94; N, 10.84.

578743-87-0 [1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper chloride 0, acopper-catalyst compound, is more and more widely used in various.

Reference£º
Patent; THE UNIVERSITY OF SOUTHERN CALIFORNIA; THOMPSON, Mark; DJUROVICH, Peter; KRYLOVA, Valentina; WO2011/63083; (2011); A1;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”