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2-<2,3,5,10-Tetrahydro-1,1,3,3-tetramethyl-10-oxo-1H-cyclopentacridin-5-yl>benzoesaeure-methylester

Base Information Edit
  • Chemical Name:2-<2,3,5,10-Tetrahydro-1,1,3,3-tetramethyl-10-oxo-1H-cyclopentacridin-5-yl>benzoesaeure-methylester
  • CAS No.:73183-86-5
  • Molecular Formula:C28H27NO3
  • Molecular Weight:425.527
  • Hs Code.:
  • Mol file:73183-86-5.mol
2-<2,3,5,10-Tetrahydro-1,1,3,3-tetramethyl-10-oxo-1H-cyclopent<b>acridin-5-yl>benzoesaeure-methylester

Synonyms:

Suppliers and Price of 2-<2,3,5,10-Tetrahydro-1,1,3,3-tetramethyl-10-oxo-1H-cyclopentacridin-5-yl>benzoesaeure-methylester
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2-<2,3,5,10-Tetrahydro-1,1,3,3-tetramethyl-10-oxo-1H-cyclopentacridin-5-yl>benzoesaeure-methylester Edit
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Technology Process of 2-<2,3,5,10-Tetrahydro-1,1,3,3-tetramethyl-10-oxo-1H-cyclopentacridin-5-yl>benzoesaeure-methylester

There total 8 articles about 2-<2,3,5,10-Tetrahydro-1,1,3,3-tetramethyl-10-oxo-1H-cyclopentacridin-5-yl>benzoesaeure-methylester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 7 steps
1: 47 percent / NaNO2, conc. HNO3 / acetic acid / 0.25 h / 10 - 20 °C
2: 88 percent / sat. aq. NH3, NH4Cl / 20 h / 140 - 150 °C / 18751.5 Torr
3: 24 percent / K2CO3 / Naturkupfer C
4: 58 percent / H2 / Raney-nickel / ethyl acetate / 24 h
5: NaNO2, conc. HCl / H2O / 0 °C
6: 45percent hypophosphoric acid / 1) refrigerator, 8 h, 2) room temp., 8 h
7: 55 percent / PPA / 4 h / 130 - 140 °C
With hydrogenchloride; ammonium hydroxide; hydrogen; nitric acid; potassium carbonate; ammonium chloride; hypophosphoric acid; sodium nitrite; Naturkupfer C; nickel; In water; acetic acid; ethyl acetate;
Guidance literature:
Multi-step reaction with 5 steps
1: 24 percent / K2CO3 / Naturkupfer C
2: 58 percent / H2 / Raney-nickel / ethyl acetate / 24 h
3: NaNO2, conc. HCl / H2O / 0 °C
4: 45percent hypophosphoric acid / 1) refrigerator, 8 h, 2) room temp., 8 h
5: 55 percent / PPA / 4 h / 130 - 140 °C
With hydrogenchloride; hydrogen; potassium carbonate; hypophosphoric acid; sodium nitrite; Naturkupfer C; nickel; In water; ethyl acetate;
Refernces Edit
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