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2,2-dimethyl-5-[2-(4-octylphenyl)ethyl]-1,3-dioxan-5-amine

Base Information Edit
  • Chemical Name:2,2-dimethyl-5-[2-(4-octylphenyl)ethyl]-1,3-dioxan-5-amine
  • CAS No.:1313876-85-5
  • Molecular Formula:C22H37NO2
  • Molecular Weight:347.541
  • Hs Code.:
  • Mol file:1313876-85-5.mol
2,2-dimethyl-5-[2-(4-octylphenyl)ethyl]-1,3-dioxan-5-amine

Synonyms:2,2-dimethyl-5-[2-(4-octylphenyl)ethyl]-1,3-dioxan-5-amine

Suppliers and Price of 2,2-dimethyl-5-[2-(4-octylphenyl)ethyl]-1,3-dioxan-5-amine
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 2,2-Dimethyl-5-[2-(4-octylphenyl)ethyl]-1,3-dioxan-5-amine
  • 50mg
  • $ 510.00
Total 1 raw suppliers
Chemical Property of 2,2-dimethyl-5-[2-(4-octylphenyl)ethyl]-1,3-dioxan-5-amine Edit
Chemical Property:
Purity/Quality:

95%-98% *data from raw suppliers

2,2-Dimethyl-5-[2-(4-octylphenyl)ethyl]-1,3-dioxan-5-amine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 2,2-Dimethyl-5-[2-(4-octylphenyl)ethyl]-1,3-dioxan-5-amine is an intermediate in the synthesis of N-[2(4-(-Octylphenyl))butanoic Acid] Fingolimod,which is an impurity of Fingolimod (F805000, HCl salt). Fingolimod is a novel immune modulator that prolongs allograft transplant survival in numerous models by inhibiting lymphocyte emigration from lymphoid organs.
Technology Process of 2,2-dimethyl-5-[2-(4-octylphenyl)ethyl]-1,3-dioxan-5-amine

There total 11 articles about 2,2-dimethyl-5-[2-(4-octylphenyl)ethyl]-1,3-dioxan-5-amine 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:
With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 3h;
DOI:10.1007/s00706-011-0582-7
Guidance literature:
Multi-step reaction with 3 steps
1: toluene / 6 h / Reflux; Inert atmosphere
2: potassium carbonate / tetrahydrofuran; N,N-dimethyl-formamide / 20 h / Reflux
3: palladium 10% on activated carbon; hydrogen / methanol / 3 h / 20 °C
With palladium 10% on activated carbon; hydrogen; potassium carbonate; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene; 2: Wittig reaction;
DOI:10.1007/s00706-011-0582-7
Guidance literature:
Multi-step reaction with 3 steps
1: 3-chloro-benzenecarboperoxoic acid / chloroform / 4 h / 20 °C / Cooling with ice
2: potassium carbonate / N,N-dimethyl-formamide; tetrahydrofuran / 6 h / Reflux
3: hydrogen / palladium 10% on activated carbon / methanol / 2 h / 20 °C
With hydrogen; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; palladium 10% on activated carbon; In tetrahydrofuran; methanol; chloroform; N,N-dimethyl-formamide; 2: Knoevenagel Condensation;
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