Month: August 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.

General procedure: Representative procedure for 17: A Schlenk tube was charged with 2 (400mg, 2.03mmol), dry THF (10mL), anhydrous cobalt(II) chloride and a stirring bar. In a separate Schlenk tube, a solution of lithium diisopropylamide (LDA) was prepared in THF (25mL) from diisopropylamine (700muL, 5.0 mmol) and n-butyl lithium (3.15mL of a 1.6M solution in hexane, 5.0 mmol). The LDA-solution was added under protection from air to the solution of 2 and CoCl2. After the mixture has been stirred overnight, all volatile materials were removed on a vacuum line. The Schlenk vessel was transferred into the glove-box and the dark colored solid residue was dissolved in a small volume of dry dichloromethane. Layering the solution with dry n-hexane afforded brown single crystals of the product.

34946-82-2 Copper(II) trifluoromethanesulfonate 2734996, acopper-catalyst compound, is more and more widely used in various.

Reference£º
Article; Graser, Markus; Kopacka, Holger; Wurst, Klaus; Mueller, Thomas; Bildstein, Benno; Inorganica Chimica Acta; vol. 401; (2013); p. 38 – 49;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

34946-82-2, Copper(II) trifluoromethanesulfonate is a copper-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

A methanolic solution of ligand trans-cyclohexane-1,2-diamine(0.1142 g, 1 mmol) was added dropwise to a clear solution ofCopper(II) trifluoromethanesulfonate (0.1808 g, 0.5 mmol) inmethanol (10 mL). The resultant solution was stirred at roomtemperature for 6 h to produce a dark blue coloured solution. Thediffraction quality crystals of the titled complex were obtaineddirectly by slow evaporation of the deep bluish methanolic solutionat room temperature. Yield: 0.272 g, 75%, m.p: 258 C, Anal. Calc. forC14H32CuF6N4O8S2: C, 26.86; H, 5.15; N, 8.95. Found: C, 26.54; H,5.32, N, 8.78. Selected FT-IR (KBr), cm1: n(NH2) 3332e3279, n(CH2)2967e2861, n(OH) 3463, n(CueN) 628, n(CueO) 514. UVeVis [lmax(nm), epsilon (L mol1 cm1)]: 243 (8940), 548 (89).

As the paragraph descriping shows that 34946-82-2 is playing an increasingly important role.

Reference£º
Article; Agrahari, Bhumika; Layek, Samaresh; Kumari, Shweta; Anuradha; Ganguly, Rakesh; Pathak, Devendra D.; Journal of Molecular Structure; vol. 1134; (2017); p. 85 – 90;,
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.

For the synthesis of (I), a solution of BDPA (0.160 g,0.554 mmol) in THF (6.0 ml) was added to a solution of Cu(triflate)2 (0.200 g, 0.554 mmol) in THF (6.0 ml) and theresulting mixture was stirred for 12 h. The resulting palegreen-palegreen-blue solution was concentrated under reduced pressure,affording a pale-green-blue solid which was dried under high vacuum. The solid was dissolved in THF and diffused withdiethyl ether, giving blue block-shaped crystals after 5 d(yield: 0.102 g, 26%). Elemental analysis calculated: C 40.51,H 3.94, N 5.67, S 8.65%; found: C 40.31, H 3.79, N 5.62; S8.69%. FT-IR (KBr, cm-1); 3374 (m), 3092 (w), 3030 (w), 2965(w), 2969 (m), 2880 (w), 1657 (m), 1612 (s), 1484 (m), 1450 (s),1358 (w), 1288 (s), 1250 (s), 1168 (s), 1030 (s), 860 (m), 771(m), 706 (m), 635 (s).

34946-82-2 Copper(II) trifluoromethanesulfonate 2734996, acopper-catalyst compound, is more and more widely used in various.

Reference£º
Article; Sivanesan, Dharmalingam; Youn, Min Hye; Park, Ki Tae; Kim, Hak Joo; Grace, Andrews Nirmala; Jeong, Soon Kwan; Acta Crystallographica Section C: Structural Chemistry; vol. 73; 11; (2017); p. 1024 – 1029;,
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.

Ligand L2/L2? (15.2 mg, 63 mumol) was dissolved in ethylacetate (5 mL) and a solution of Cu(OTf)2 (11.4 mg, 31.5mumol) in ethyl acetate (3 mL) was added. The blue precipitatewas isolated by filtration with suction and dried at air;yield: 26 mg (98%). Crystals suitable for X-ray diffractionanalysis were obtained when a solution of the precipitatein the necessary amount of ethyl acetate was concentratedby slow evaporation. M.p. 255.5-256.5C. – IR (KBr): IR(KBr): = 3259 s br (NH), 3151 w, 1643 m, 1591 s, 1500 m,1285 vs, 1243 vs, ~1228 sh, 1159 s, 1028 vs, 720 m, 636 s,574 w, 518 m cm-1. – MS ((+)-MALDI-TOF): m/z (%) = 694.15(100) [M-CF3SO3]+, 1539.24 (8) [2 [CuL2L2?(OTf)2]-OTf]. -Anal. for C28H30CuF6N10O6S2 (844.27), water-free sample:calcd. C 39.83, H 3.58, N 16.59; S 7.59; found C 39.62, H 3.41,N 16.64, S 7.61.

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

Reference£º
Article; Schroeder, Sven; Frey, Wolfgang; Maas, Gerhard; Zeitschrift fur Naturforschung, B: Chemical Sciences; vol. 71; 6; (2016); p. 683 – 696;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

34946-82-2, Copper(II) trifluoromethanesulfonate is a copper-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

A solution of Cu(OTf)2 (90.0 mg, 0.249 mM) in methanol was added to a solution of HLpz (57.0 mg, 0.250 mM) and triethylamine (25.0 mg, 0.250 mM) in methanol, affording a dark blue solution. A solution of NaN3 (16.3 mg, 0.250 mM) was then layered on the above solution from which blue crystals of 4 suitable for X-ray analysis were obtained (54 mg, 65% yield). Anal. Calcd for C12H11CuN7O: C,43.31; H, 3.33; N, 29.46. Found: C, 43.68; H, 3.35; N, 29.59. UV-vis (CH3OH) lambdamax, nm(epsilon, M-1 cm-1)]: 346 (5000), 637 (240). FTIR (KBr): 2855, 2054, 1624, 1366, 1168, 1043,773 cm-1. EPR (9.447 GHz, Mod. Amp. 5.0 G, CH3OH, 77 K): g|| = 2.249, g? 2:037,and A|| = 170 G. ESI-MS (MeOH): m/z = 355 [Cu(Lpz)N3 + Na]+, 687 {[Cu(Lpz)N3]2 + Na}+, 1019 {[Cu(Lpz)N3]3 + Na}+.

As the paragraph descriping shows that 34946-82-2 is playing an increasingly important role.

Reference£º
Article; Houser, Robert P.; Wang, Zhaodong; Powell, Douglas R.; Hubin, Timothy J.; Journal of Coordination Chemistry; vol. 66; 23; (2013); p. 4080 – 4092;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

13395-16-9, Bis(acetylacetone)copper is a copper-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: The monodisperse CuPd alloy NPs with composition controlwere synthesized by using a modified version of our estab-lished recipe for the CoPd alloy NPs [14]. In a typical synthesis of Cu75Pd25NPs, copper(II) acetylacetonate (0.35 mmol, 90 mg)and palladium(II) acetylacetonate (0.1 mmol, 31 mg) were dis-solved in 3 mL of OAm in a 10 mL of glass vial. In a four-necked glass reactor that allows to study under inert atmosphere,200 mg of MB was dissolved in 3 mL of OAm and 7 mL of 1-octadecene at 80C under magnetic stirring. Next, the metal precursor mixture was quickly injected into the reactor under argon environment. The reaction was then proceed for 1 h before cooled down to room temperature. Then, the colloidal NPs mixture was transferred into two separate centrifuge tubeand acetone/ethanol (v/v = 7/3) was added into the tubes. TheNP product was separated by centrifugation at 8500 rpm for10 min.

The synthetic route of 13395-16-9 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Guengoermez, Kuebra; Metin, Oender; Applied Catalysis A: General; vol. 494; (2015); p. 22 – 28;,
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: 0.028g (0.283mmol) of CuCl was added to 0.220g (0.133mmol) of [PPh4]2[1] dissolved in 20mL of MeCN solution. After stirring the resultant solution for 1hat RT, the yellowish brown solution formed. The solution was filtered, and the solvent was removed in vacuo. The precipitate was washed with Et2O and MeOH and extracted with CH2Cl2 which was then recrystallized with Et2O/MeOH/CH2Cl2 to give [PPh4]2[5a] (0.110g, 0.064mmol, 96% based on Se). Similarly, under the same reaction conditions, using CuBr and CuI, we have isolated a yellowish brown solid of [PPh4]2[5b] (98% based on Se) and [PPh4]2[5c] (71% based on Se), respectively, upon crystallization from Et2O/MeOH/CH2Cl2. [PPN]2[5a] and [PPN]2[5c] were synthesized according to a similar procedure.

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

Reference£º
Article; Shieh, Minghuey; Miu, Chia-Yeh; Liu, Yu-Hsin; Chu, Yen-Yi; Hsing, Kai-Jieah; Chiu, Jung-I; Lee, Chung-Feng; Journal of Organometallic Chemistry; vol. 815-816; (2016); p. 74 – 83;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

13395-16-9, Bis(acetylacetone)copper is a copper-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

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.

The synthetic route of 13395-16-9 has been constantly updated, and we look forward to future research findings.

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”

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

A mixture of 2 (55mg, 0.13mmol) and Ag2O (18.5mg, 0.08mmol) in a 5mL flask was flashed with nitrogen. Anhydrous acetonitrile (1.5mL) was added and the resulting mixture was heated at 65C for 20h. CuBr2 (29.5mg, 0.13 3mmol) and K2CO3 (18.3mg, 0.13mmol) was added to the above solution. After stirring for another 20h, the mixture was filtered through Celite. The filtrate was concentrated and the residue was re-precipitated from acetonitrile/ether to give dark purple solids (240mg, 70%). IR (CHCl3) upsilon(C=O) 1595cm-1. UV-Vis (MeOH) lambdamax (epsilon): 219 (1.0¡Á104), 250 (5.2¡Á103), 340 (sh, 1.3¡Á103), 381 (sh, 5.4¡Á102) and 640 (79) nm; mueff=1.71 muB (295K); HRMS (ESI): m/z 396.1088 [M-Br]+, calcd. 396.1017.

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

Reference£º
Article; Aaron Lin, Shih-Chieh; Liu, Yi-Hung; Peng, Shie-Ming; Liu, Shiuh-Tzung; Journal of Organometallic Chemistry; vol. 859; (2018); p. 52 – 57;,
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.

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”