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N-trifluoroacetyl-(R)-1-aminoindan

Base Information Edit
  • Chemical Name:N-trifluoroacetyl-(R)-1-aminoindan
  • CAS No.:155666-94-7
  • Molecular Formula:C11H10F3NO
  • Molecular Weight:229.202
  • Hs Code.:
  • Mol file:155666-94-7.mol
N-trifluoroacetyl-(R)-1-aminoindan

Synonyms:N-trifluoroacetyl-(R)-1-aminoindan

Suppliers and Price of N-trifluoroacetyl-(R)-1-aminoindan
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
  • (-)-N-Trifluoroacetyl-1-aminoindan
  • 500mg
  • $ 1605.00
  • TRC
  • (-)-N-Trifluoroacetyl-1-aminoindan
  • 250mg
  • $ 915.00
  • TRC
  • (-)-N-Trifluoroacetyl-1-aminoindan
  • 100mg
  • $ 375.00
  • TRC
  • (-)-N-Trifluoroacetyl-1-aminoindan
  • 50mg
  • $ 200.00
  • TRC
  • (-)-N-Trifluoroacetyl-1-aminoindan
  • 25mg
  • $ 110.00
Total 2 raw suppliers
Chemical Property of N-trifluoroacetyl-(R)-1-aminoindan Edit
Chemical Property:
Purity/Quality:

98% *data from raw suppliers

(-)-N-Trifluoroacetyl-1-aminoindan *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses (-)-N-Trifluoroacetyl-1-aminoindan is an intermediate in the synthesis of (3R)-2,3-Dihydro-3-(2-propyn-1-ylamino)-1H-inden-1-one (D449765), which is a building block in the preparation of Rasagiline (R126000), which is a selective irreversible MAO-B inhibitor. Rasagiline is also an Antiparkinsonian agent.
Technology Process of N-trifluoroacetyl-(R)-1-aminoindan

There total 7 articles about N-trifluoroacetyl-(R)-1-aminoindan 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 pyridine; In dichloromethane; at 20 ℃; for 0.583333h; Ice bath;
Guidance literature:
With potassium hydroxide; In toluene; at 20 ℃; for 2h;
DOI:10.1021/jm020120c
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