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N-CBZ-NORTROPINE

Base Information
  • Chemical Name:N-CBZ-NORTROPINE
  • CAS No.:92652-76-1
  • Molecular Formula:C15H19 N O3
  • Molecular Weight:261.32
  • Hs Code.:2933990090
  • Mol file:92652-76-1.mol
N-CBZ-NORTROPINE

Synonyms:8-Nortropanecarboxylicacid, 3-hydroxy-, benzyl ester (7CI)

Suppliers and Price of N-CBZ-NORTROPINE
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
  • Crysdot
  • Benzyl3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate 95+%
  • 1g
  • $ 185.00
  • Crysdot
  • Benzyl3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate 95+%
  • 25g
  • $ 646.00
  • Chemenu
  • Benzyl3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate 95%
  • 25g
  • $ 604.00
  • American Custom Chemicals Corporation
  • 3-HYDROXY-8-AZA-BICYCLO[3.2.1]OCTANE-8-CARBOXYLIC ACID BENZYL ESTER 95.00%
  • 5G
  • $ 1210.32
  • Alichem
  • Benzyl3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate
  • 10g
  • $ 238.96
  • Alichem
  • Benzyl3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate
  • 5g
  • $ 154.00
Total 21 raw suppliers
Chemical Property of N-CBZ-NORTROPINE
Chemical Property:
  • Melting Point:124 °C(Solv: benzene (71-43-2)) 
  • Boiling Point:416.4±45.0 °C(Predicted) 
  • PKA:14.78±0.20(Predicted) 
  • PSA:49.77000 
  • Density:1.248±0.06 g/cm3(Predicted) 
  • LogP:2.24880 
  • Storage Temp.:2-8°C 
Purity/Quality:

97% *data from raw suppliers

Benzyl3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of N-CBZ-NORTROPINE

There total 2 articles about N-CBZ-NORTROPINE 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:
Aus Nortropanol-(3α) u. Benzyloxycarbonylchlorid;
DOI:10.1021/jm50014a011
Guidance literature:
Nortropanol-(3α), Benzyloxycarbonylchlorid;
DOI:10.1021/jm50014a011
Guidance literature:
With 1H-imidazole; iodine; triphenylphosphine; In dichloromethane; at 0 ℃; for 0.5h;
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