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5-Chloro-1-aza-5-stannabicyclo[3.3.3]undecane

Base Information
  • Chemical Name:5-Chloro-1-aza-5-stannabicyclo[3.3.3]undecane
  • CAS No.:93253-73-7
  • Molecular Formula:C9H18ClNSn
  • Molecular Weight:294.412
  • Hs Code.:
  • European Community (EC) Number:632-985-3
  • DSSTox Substance ID:DTXSID60454424
  • Mol file:93253-73-7.mol
5-Chloro-1-aza-5-stannabicyclo[3.3.3]undecane

Synonyms:5-chloro-1-aza-5-stannabicyclo[3.3.3]undecane;93253-73-7;5-Chloro-1-aza-5-stanna-bicyclo[3.3.3]undecane;1-Aza-5-stannabicyclo[3.3.3]undecane, 5-chloro-;SCHEMBL5727023;DTXSID60454424

Suppliers and Price of 5-Chloro-1-aza-5-stannabicyclo[3.3.3]undecane
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
  • Sigma-Aldrich
  • 5-Chloro-1-aza-5-stanna-bicyclo[3.3.3]undecane
  • 2g
  • $ 487.00
  • Sigma-Aldrich
  • 5-Chloro-1-aza-5-stanna-bicyclo[3.3.3]undecane
  • 500mg
  • $ 145.00
  • American Custom Chemicals Corporation
  • 5-CHLORO-1-AZA-5-STANNA-BICYCLO[3.3.3]UNDECANE 95.00%
  • 2G
  • $ 1072.42
  • American Custom Chemicals Corporation
  • 5-CHLORO-1-AZA-5-STANNA-BICYCLO[3.3.3]UNDECANE 95.00%
  • 500MG
  • $ 661.44
Total 4 raw suppliers
Chemical Property of 5-Chloro-1-aza-5-stannabicyclo[3.3.3]undecane
Chemical Property:
  • Melting Point:226-230°C 
  • PSA:3.24000 
  • LogP:-2.21890 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:295.014980
  • Heavy Atom Count:12
  • Complexity:136
Purity/Quality:

5-Chloro-1-aza-5-stanna-bicyclo[3.3.3]undecane *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:T,N 
  • Statements: 21-25-36/38-48/23/25-50/53 
  • Safety Statements: 35-36/37/39-45-60-61 
MSDS Files:
Useful:
  • Canonical SMILES:C1CN2CCC[Sn](C1)(CCC2)Cl
  • Uses Reactant for:Metal-catalyzed allylic substitution reactionSynthesis of an anti-methicillin-resistant staphylococcus aureus (MRSA) carbapenem via stannatrane mediated Stille coupling
Technology Process of 5-Chloro-1-aza-5-stannabicyclo[3.3.3]undecane

There total 5 articles about 5-Chloro-1-aza-5-stannabicyclo[3.3.3]undecane 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 Schwartz's reagent; In tetrahydrofuran; hydrozirconation of triallylamine; purging flask with N2, charging with (C5H5)2ZrHCl, dry THF and N,N,N-triallylamine, stirring 3 h at 23°C, cooling to -78°C, treatment with freshly distd. SnCl4, warming to 23°C over 4 h;; addn. of mixt. to H2O after 14 h, extracting twice with C2H5O2CCH3, drying over Na2SO4, filtration, evaporation, recrystn. from CH3OH;;
DOI:10.1021/ja00042a044
Guidance literature:
In neat (no solvent); byproducts: Me3SnCl; heated to 150°C for 10 h and to 190°C for 6 h; distn. (Me3SnCl), sublimation of the residue (150-160°C/10 Torr), recrystn. (ethanol); elem. anal.;
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