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(3R,3'R,4R,4'R)-3,3',4,4'-tetrakis(3,5-dimethylphenyl)-1,1'-ethylenedipyrrolidine

Base Information
  • Chemical Name:(3R,3'R,4R,4'R)-3,3',4,4'-tetrakis(3,5-dimethylphenyl)-1,1'-ethylenedipyrrolidine
  • CAS No.:109297-17-8
  • Molecular Formula:C42H52N2
  • Molecular Weight:584.888
  • Hs Code.:
(3R,3'R,4R,4'R)-3,3',4,4'-tetrakis(3,5-dimethylphenyl)-1,1'-ethylenedipyrrolidine

Synonyms:(3R,3'R,4R,4'R)-3,3',4,4'-tetrakis(3,5-dimethylphenyl)-1,1'-ethylenedipyrrolidine

Suppliers and Price of (3R,3'R,4R,4'R)-3,3',4,4'-tetrakis(3,5-dimethylphenyl)-1,1'-ethylenedipyrrolidine
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Chemical Property of (3R,3'R,4R,4'R)-3,3',4,4'-tetrakis(3,5-dimethylphenyl)-1,1'-ethylenedipyrrolidine
Chemical Property:
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Technology Process of (3R,3'R,4R,4'R)-3,3',4,4'-tetrakis(3,5-dimethylphenyl)-1,1'-ethylenedipyrrolidine

There total 12 articles about (3R,3'R,4R,4'R)-3,3',4,4'-tetrakis(3,5-dimethylphenyl)-1,1'-ethylenedipyrrolidine 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 6 steps
1: 48 percent / benzene / 5 h / Ambient temperature
2: 68 percent / conc. HCl, acetic acid / 24 h / Heating
3: LiAlH4 / tetrahydrofuran / 1 h / Heating
4: 76 percent / formic acid / Pd-C (10percent) / methanol / 48 h
5: 77 percent / Et3N / CH2Cl2 / 0.17 h / Ambient temperature
6: 84 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating
With hydrogenchloride; lithium aluminium tetrahydride; formic acid; acetic acid; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; benzene;
DOI:10.1016/S0040-4020(01)80176-9
Guidance literature:
Multi-step reaction with 9 steps
1: 50 percent / NaCN / H2O; methanol / 15 h / Heating
2: 60 percent / 98percent H2SO4 / ethanol / 48 h / Heating
3: 78 percent / acetyl chloride / 12 h / Ambient temperature
4: 48 percent / benzene / 5 h / Ambient temperature
5: 68 percent / conc. HCl, acetic acid / 24 h / Heating
6: LiAlH4 / tetrahydrofuran / 1 h / Heating
7: 76 percent / formic acid / Pd-C (10percent) / methanol / 48 h
8: 77 percent / Et3N / CH2Cl2 / 0.17 h / Ambient temperature
9: 84 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating
With hydrogenchloride; lithium aluminium tetrahydride; formic acid; sulfuric acid; sodium cyanide; acetic acid; triethylamine; acetyl chloride; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; benzene;
DOI:10.1016/S0040-4020(01)80176-9
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