Nitrosocyclohexane

Base Information

Chemical Name:Nitrosocyclohexane
CAS No.:2696-95-9
Molecular Formula:C6H11NO
Molecular Weight:113.159
Hs Code.:
DSSTox Substance ID:DTXSID90472015
Nikkaji Number:J478.700E
Wikidata:Q82300756

Synonyms:Nitrosocyclohexane;SCHEMBL249058;DTXSID90472015;AFLQDEOAJRGCOW-UHFFFAOYSA-N

Suppliers and Price of Nitrosocyclohexane

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 11 raw suppliers

Chemical Property of Nitrosocyclohexane

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:113.084063974
Heavy Atom Count:8
Complexity:76.6

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(CC1)N=O

Technology Process of Nitrosocyclohexane

There total 5 articles about Nitrosocyclohexane 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: 93.0%

: 2211-64-5
N-cyclohexyl-hydroxylamine

: 2696-95-9
nitrosocyclohexane

Guidance literature:: With carbon nanotube-rhodium nanohybrid; air; In chloroform; water; at 20 ℃; for 12h;
DOI:10.1039/c5cy00985e

Reference yield: 64.0%

: 110-82-7,25012-93-5
cyclohexane

: 2696-95-9
nitrosocyclohexane

: 1122-60-7
1-nitrocyclohexane

Guidance literature:: With tert.-butylnitrite; N-hydroxyphthalimide; In tetradeuterioacetic acid; at 80 ℃; for 2h; Further Variations:; Solvents; Temperatures; Reagents; reaction times; Product distribution;
DOI:10.1002/anie.200352741