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8-Azabicyclo[3.2.1]octan-3-ol

Base Information Edit
  • Chemical Name:8-Azabicyclo[3.2.1]octan-3-ol
  • CAS No.:14383-51-8
  • Molecular Formula:C7H13NO.HCl
  • Molecular Weight:163.647
  • Hs Code.:2933990090
  • European Community (EC) Number:238-356-6,826-257-6
  • NSC Number:241188,72850
  • DSSTox Substance ID:DTXSID40964516
  • Nikkaji Number:J36.172K
  • Wikidata:Q82946520
  • Metabolomics Workbench ID:45027
  • Mol file:14383-51-8.mol
8-Azabicyclo[3.2.1]octan-3-ol

Synonyms:8-Azabicyclo[3.2.1]octan-3-ol;Nortropin;7432-11-3;Tropigenin;Tropigenine;Norpseudotropine;Nor-psi-tropine;3-beta-Nortropanol;Pseudonortropine;Pseudotropigenine;ENDO-8-AZABICYCLO[3.2.1]OCTAN-3-OL;501-33-7;Nortropine hydrochloride;Nortropane, 3-hydroxy-;1-alpha-H,5-alpha-H-Nortropan-3-beta-ol;NSC72850;8-Azabicyclo(3.2.1)octan-3-ol, exo-;NOR-TROPANOL;14383-51-8;8-Azabicyclo-3.2.1-octan-3-ol;MFCD00047140;Nor-y-tropine;3-Hydroxy-Nortropane;8-Azabicyclo(3.2.1)octan-3-ol, exo- (9CI);8-Azabicyclo(3.2.1)octan-3-ol, endo- (9CI);SCHEMBL239951;WLN: T56 A AMTJ GQ;8-azabicyclo[3.2.1]octan3-ol;DTXSID40964516;CHEBI:165181;YYMCYJLIYNNOMK-UHFFFAOYSA-N;Nortropidine,3-dihydro-3-hydroxy-;8-aza-bicyclo[3,2,1]octan-3-ol;NSC-72850;NSC241188;AKOS009157075;NSC-241188;PB17241;PB32100;SB21649;8-Azabicyclo[3.2.1]octan-3-ol, 9CI;CS-11060;LS-97497;SY004118;2,3-DIHYDRO-3-HYDROXY-NORTROPIDINE;8-AZA-BICYCLO[3.2.1]OCTAN-3-OL;(1r,5s)-8-azabicyclo[3.2.1]octan-3-ol;FT-0601526;N0843;1.alpha.H,5.alpha.H-Nortropan-3.alpha.-ol;EN300-51588;1.alpha.-H,5.alpha.-H-Nortropan-3.alpha.-ol;F0001-1395;Z727903334;6928D77F-413B-46A7-950D-929B30F3FB24

Suppliers and Price of 8-Azabicyclo[3.2.1]octan-3-ol
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
  • Usbiological
  • Nortropine Hydrochloride
  • 250mg
  • $ 403.00
  • TRC
  • NortropineHydrochloride
  • 5g
  • $ 405.00
  • Matrix Scientific
  • Nortropine hydrochloride 95+%
  • 25g
  • $ 190.00
  • Matrix Scientific
  • Nortropine hydrochloride 95+%
  • 5g
  • $ 70.00
  • Chemenu
  • endo-8-Azabicyclo[3.2.1]octan-3-olHydrochloride 95%
  • 100g
  • $ 241.00
  • American Custom Chemicals Corporation
  • ENDO-8-AZABICYCLO(3.2.1)OCTAN-3-OL HYDROCHLORIDE 95.00%
  • 10G
  • $ 2139.06
  • American Custom Chemicals Corporation
  • ENDO-8-AZABICYCLO(3.2.1)OCTAN-3-OL HYDROCHLORIDE 95.00%
  • 5G
  • $ 1519.98
  • American Custom Chemicals Corporation
  • ENDO-8-AZABICYCLO(3.2.1)OCTAN-3-OL HYDROCHLORIDE 95.00%
  • 1G
  • $ 882.42
  • Ambeed
  • endo-8-Azabicyclo[3.2.1]octan-3-olhydrochloride 95+%
  • 1g
  • $ 34.00
  • Ambeed
  • endo-8-Azabicyclo[3.2.1]octan-3-olhydrochloride 95+%
  • 250mg
  • $ 13.00
Total 92 raw suppliers
Chemical Property of 8-Azabicyclo[3.2.1]octan-3-ol Edit
Chemical Property:
  • Appearance/Colour:Off-white solid 
  • Vapor Pressure:0.0132mmHg at 25°C 
  • Melting Point:231-237 °C (dec.) 
  • Boiling Point:266.5 °C at 760 mmHg 
  • Flash Point:115 °C 
  • PSA:32.26000 
  • LogP:1.39250 
  • Storage Temp.:Hygroscopic, -20?C Freezer, Under Inert Atmosphere 
  • Solubility.:DMSO, Water 
  • XLogP3:0.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:127.099714038
  • Heavy Atom Count:9
  • Complexity:104
Purity/Quality:

99% *data from raw suppliers

Nortropine Hydrochloride *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC2CC(CC1N2)O
  • Uses Metabolite of Atropine Metabolite of Atropine.
Technology Process of 8-Azabicyclo[3.2.1]octan-3-ol

There total 6 articles about 8-Azabicyclo[3.2.1]octan-3-ol 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 hydrogenchloride; In 1,4-dioxane; acetonitrile; at 70 ℃; for 1h;
Guidance literature:
With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 16h;
Refernces Edit
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