1-Azabicyclo[2.2.2]octane, 3-ethenyl-

Base Information

Chemical Name:1-Azabicyclo[2.2.2]octane, 3-ethenyl-
CAS No.:2643-30-3
Molecular Formula:C9H15N
Molecular Weight:137.22200
Hs Code.:
DSSTox Substance ID:DTXSID30415668
Mol file:2643-30-3.mol

Synonyms:3-vinylquinuclidine;1-Azabicyclo[2.2.2]octane, 3-ethenyl-;2643-30-3;SCHEMBL6358575;DTXSID30415668;STMXRYQUMAMCAF-UHFFFAOYSA-N

Suppliers and Price of 1-Azabicyclo[2.2.2]octane, 3-ethenyl-

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

Total 8 raw suppliers

Chemical Property of 1-Azabicyclo[2.2.2]octane, 3-ethenyl-

Chemical Property:

Melting Point:152 °C
Boiling Point:85 °C(Press: 15 Torr)
PKA:10.45±0.33(Predicted)
PSA：3.24000
Density:0.9409 g/cm3(Temp: 25 °C)
LogP:1.45210
XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:137.120449483
Heavy Atom Count:10
Complexity:134

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CC1CN2CCC1CC2

Technology Process of 1-Azabicyclo[2.2.2]octane, 3-ethenyl-

There total 4 articles about 1-Azabicyclo[2.2.2]octane, 3-ethenyl- 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:

Reference yield:

: 2643-30-3
(R)-3-vinyl-quinuclidine

Guidance literature:: With chloroform; phosphorus tribromide; Erwaermen der aus dem erhaltenen Salz freigesetzten Base mit Aethanol und Erwaermen des danach isolierten Reaktionsprodukts mit wss. Natronlauge;

Reference yield:

: 5176-21-6
1-azabicyclo[2.2.2]octane-3-carboxaldehyde

: 20667-19-0
methyltriphenylphosphonium iodide

: 2643-30-3
3-Vinylquinuclidine

Guidance literature:: With sodium amide; Yield given. Multistep reaction; 1.) liq. NH₃, 30 min, 2.) ether, 2 h, overnight;
DOI:10.1007/BF00763694