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(1s,5s)-9-azabicyclo[3.3.1]nonane hydrochloride

Base Information
  • Chemical Name:(1s,5s)-9-azabicyclo[3.3.1]nonane hydrochloride
  • CAS No.:6760-43-6
  • Molecular Formula:C8H15N.ClH
  • Molecular Weight:161.675
  • Hs Code.:2933990090
  • Mol file:6760-43-6.mol
(1s,5s)-9-azabicyclo[3.3.1]nonane hydrochloride

Synonyms:

Suppliers and Price of (1s,5s)-9-azabicyclo[3.3.1]nonane hydrochloride
Supply Marketing:
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
  • 9-azabicyclo[3.3.1]nonanehydrochloride
  • 50mg
  • $ 155.00
  • SynQuest Laboratories
  • (1s,5s)-9-Azabicyclo[3.3.1]nonanehydrochloride
  • 250 mg
  • $ 275.00
  • SynQuest Laboratories
  • (1s,5s)-9-Azabicyclo[3.3.1]nonanehydrochloride
  • 1 g
  • $ 875.00
  • J&W Pharmlab
  • 9-Aza-bicyclo[3.3.1]nonanehydrochloride 97%
  • 500mg
  • $ 299.00
  • Crysdot
  • 9-Azabicyclo[3.3.1]nonanehydrochloride 95+%
  • 1g
  • $ 698.00
  • Crysdot
  • 9-Azabicyclo[3.3.1]nonanehydrochloride 95+%
  • 5g
  • $ 2440.00
  • Chemenu
  • 9-Azabicyclo[3.3.1]nonanehydrochloride 95%
  • 5g
  • $ 2281.00
  • Chemenu
  • 9-Azabicyclo[3.3.1]nonanehydrochloride 95%
  • 1g
  • $ 653.00
Total 10 raw suppliers
Chemical Property of (1s,5s)-9-azabicyclo[3.3.1]nonane hydrochloride
Chemical Property:
  • PSA:12.03000 
  • LogP:2.81180 
  • Storage Temp.:Inert atmosphere,Room Temperature 
Purity/Quality:

97% *data from raw suppliers

9-azabicyclo[3.3.1]nonanehydrochloride *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of (1s,5s)-9-azabicyclo[3.3.1]nonane hydrochloride

There total 2 articles about (1s,5s)-9-azabicyclo[3.3.1]nonane hydrochloride 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 2 steps
1: Et3N / CH2Cl2
2: MeOH
With methanol; triethylamine; In dichloromethane;
DOI:10.1016/j.bmcl.2004.05.074
Guidance literature:
With potassium carbonate; sodium iodide; In acetonitrile; at 60 ℃; for 18h; Sealed tube;
DOI:10.1021/jacs.8b02142
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