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ENDO-N-BENZYL-ENDO-3-AMINOTROPANE

Base Information Edit
  • Chemical Name:ENDO-N-BENZYL-ENDO-3-AMINOTROPANE
  • CAS No.:63930-14-3
  • Molecular Formula:C14H20N2
  • Molecular Weight:216.326
  • Hs Code.:
  • Mol file:63930-14-3.mol
ENDO-N-BENZYL-ENDO-3-AMINOTROPANE

Synonyms:8-Azabicyclo[3.2.1]octan-3-amine,8-methyl-N-phenyl-, exo-

Suppliers and Price of ENDO-N-BENZYL-ENDO-3-AMINOTROPANE
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
  • American Custom Chemicals Corporation
  • (3-EXO)-8-METHYL-N-PHENYL-8-AZABICYCLO[3.2.1]OCTAN-3-AMINE 95.00%
  • 5MG
  • $ 501.51
  • American Custom Chemicals Corporation
  • ENDO-N-BENZYL-ENDO-3-AMINOTROPANE 95.00%
  • 5MG
  • $ 495.40
Total 4 raw suppliers
Chemical Property of ENDO-N-BENZYL-ENDO-3-AMINOTROPANE Edit
Chemical Property:
  • PSA:15.27000 
  • LogP:2.73460 
Purity/Quality:

99% *data from raw suppliers

(3-EXO)-8-METHYL-N-PHENYL-8-AZABICYCLO[3.2.1]OCTAN-3-AMINE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of ENDO-N-BENZYL-ENDO-3-AMINOTROPANE

There total 1 articles about ENDO-N-BENZYL-ENDO-3-AMINOTROPANE 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:
Tropinon, Anilin, NaOEt (neben α-Isomer 4);
Guidance literature:
Multi-step reaction with 5 steps
1.1: Pd2dba3; (tBu)3P; NaOtBu / toluene
2.1: 6 N aq. HCl
3.1: 100 percent / HATU
4.1: 1-chloroethylchloroformate / 1,2-dichloro-ethane / 2 h / Heating
4.2: MeOH / Heating
5.1: NaBH(OAc)3 / 1,2-dichloro-ethane
With hydrogenchloride; tris-(dibenzylideneacetone)dipalladium(0); tri-tert-butyl phosphine; carbonochloridic acid 1-chloro-ethyl ester; sodium tris(acetoxy)borohydride; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; sodium t-butanolate; In 1,2-dichloro-ethane; toluene; 1.1: Arylation / 2.1: Hydrolysis / 3.1: Acylation / 4.1: quaternization / 4.2: demethylation / 5.1: reductive alkylation;
DOI:10.1016/S0960-894X(00)00182-7
Guidance literature:
Multi-step reaction with 3 steps
1: Pd2dba3; (tBu)3P; NaOtBu / toluene
2: 6 N aq. HCl
3: 100 percent / HATU
With hydrogenchloride; tris-(dibenzylideneacetone)dipalladium(0); tri-tert-butyl phosphine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; sodium t-butanolate; In toluene; 1: Arylation / 2: Hydrolysis / 3: Acylation;
DOI:10.1016/S0960-894X(00)00182-7
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