2-Iminocyclopentanecarbonitrile

Base Information Edit

Chemical Name:2-Iminocyclopentanecarbonitrile
CAS No.:2321-76-8
Molecular Formula:C6H8 N2
Molecular Weight:108.143
Hs Code.:2926909090
European Community (EC) Number:219-033-9
NSC Number:141554
DSSTox Substance ID:DTXSID701310001
Nikkaji Number:J48.252H
Mol file:2321-76-8.mol

Synonyms:2-Iminocyclopentanecarbonitrile;2321-76-8;2-iminocyclopentane-1-carbonitrile;2-Cyanocyclopentylidenimine;2-Cyanocyclopentanone imine;USAF A-1967;CYCLOPENTANECARBONITRILE, 2-IMINO-;EINECS 219-033-9;NSC 141554;1-cyano-2-iminocyclopentane;BRN 2689609;NSC141554;2-Cyanocyclopentaneimine;1-Imino-2-cyanocyclopentane;WLN: L5YTJ AUM BCN;SCHEMBL388063;2-Imino-1-cyclopentanecarbonitrile;DTXSID701310001;2-imino-cyclopentane-1-carbonitrile;AKOS006275348;LS-57832

Suppliers and Price of 2-Iminocyclopentanecarbonitrile

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

CHESS?
KH000268:2-IMINO-CYCLOPENTANECARBONITRILE 95
1 g
$ 336.00

Total 6 raw suppliers

Chemical Property of 2-Iminocyclopentanecarbonitrile Edit

Chemical Property:

Vapor Pressure:0.000308mmHg at 25°C
Melting Point:147 °C
Boiling Point:320.9°Cat760mmHg
PKA:9.67±0.40(Predicted)
Flash Point:147.9°C
PSA：47.64000
Density:1.15g/cm³
LogP:1.42958
XLogP3:0.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:108.068748264
Heavy Atom Count:8
Complexity:151

Purity/Quality:

99% ^*data from raw suppliers

KH000268:2-IMINO-CYCLOPENTANECARBONITRILE 95 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C1CC(C(=N)C1)C#N

Technology Process of 2-Iminocyclopentanecarbonitrile

There total 10 articles about 2-Iminocyclopentanecarbonitrile 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: 86.0%