Cyclohexanimine, 2,6-dimethyl-

Base Information

Chemical Name:Cyclohexanimine, 2,6-dimethyl-
CAS No.:13652-33-0
Molecular Formula:C₈H₁₅N
Molecular Weight:125.214
Hs Code.:2925290090
DSSTox Substance ID:DTXSID20884627
Nikkaji Number:J421.890F
Mol file:13652-33-0.mol

Synonyms:Cyclohexanimine, 2,6-dimethyl-;2,6-dimethylcyclohexan-1-imine;13652-33-0;2,6-Dimethylcyclohexylimine;2,6-dimethylcyclohexanimine;SCHEMBL11221646;DTXSID20884627

Suppliers and Price of Cyclohexanimine, 2,6-dimethyl-

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 3 raw suppliers

Chemical Property of Cyclohexanimine, 2,6-dimethyl-

Chemical Property:

Vapor Pressure:0.172mmHg at 25°C
Boiling Point:219.9°Cat760mmHg
Flash Point:86.8°C
PSA：23.85000
Density:0.98g/cm³
LogP:2.56200
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:125.120449483
Heavy Atom Count:9
Complexity:106

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCCC(C1=N)C

Technology Process of Cyclohexanimine, 2,6-dimethyl-

There total 2 articles about Cyclohexanimine, 2,6-dimethyl- 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:

: 2816-57-1
2,6-dimethylcyclohexanone

: 13652-33-0
2,6-Dimethyl-cyclohexylideneamine

Guidance literature:: With N-trimethylsilyl(triphenylphosphoranylidene)amine; toluene-4-sulfonic acid; In isopropyl alcohol; benzene;
DOI:10.1021/jo00401a037