N-Cyclohexylhydroxylamine

Base Information

Chemical Name:N-Cyclohexylhydroxylamine
CAS No.:2211-64-5
Molecular Formula:C6H13 N O
Molecular Weight:115.175
Hs Code.:2928000090
European Community (EC) Number:218-650-0
UNII:722GHL96BJ
DSSTox Substance ID:DTXSID90176627
Nikkaji Number:J3.389H
Wikidata:Q27266009
Mol file:2211-64-5.mol

Synonyms:N-hydroxycyclohexylamine

Suppliers and Price of N-Cyclohexylhydroxylamine

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
N-Cyclohexylhydroxylamine
1g
$ 126.00

Crysdot
N-Cyclohexylhydroxylamine 95+%
5g
$ 297.00

Crysdot
N-Cyclohexylhydroxylamine 95+%
10g
$ 475.00

Chemenu
N-Cyclohexylhydroxylamine 95%
1g
$ 102.00

Chemenu
N-Cyclohexylhydroxylamine 95%
10g
$ 449.00

Chemenu
N-Cyclohexylhydroxylamine 95%
5g
$ 281.00

Biosynth Carbosynth
N-Cyclohexylhydroxylamine
1 g
$ 220.00

Biosynth Carbosynth
N-Cyclohexylhydroxylamine
500 mg
$ 140.00

Biosynth Carbosynth
N-Cyclohexylhydroxylamine
2 g
$ 352.00

Biosynth Carbosynth
N-Cyclohexylhydroxylamine
250 mg
$ 87.50

Total 27 raw suppliers

Chemical Property of N-Cyclohexylhydroxylamine

Chemical Property:

Vapor Pressure:0.0578mmHg at 25°C
Melting Point:139-140 °C(lit.)
Refractive Index:1.4690 (estimate)
Boiling Point:205.9°Cat760mmHg
Flash Point:97.9°C
PSA：32.26000
Density:1g/cm³
LogP:1.68880
Storage Temp.:?20°C
XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:115.099714038
Heavy Atom Count:8
Complexity:59.5

Purity/Quality:

99% ^*data from raw suppliers

N-Cyclohexylhydroxylamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xn
Statements: 22-41
Safety Statements: 26-39

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(CC1)NO
Uses N-Cyclohexylhydroxylamine is a reactant for:Aldehyde-catalyzed intermolecular hydroamination1? ;Condensation reactions2? ;Preparation of cyclin-dependent kinase inhibitors selective for multiple cyclin-dependent kinases for potential use as antitumor agents3? ;Preparation of hydroxyurea derivatives as small molecule bradykinin B1 receptor antagonists. Reactant for:Aldehyde-catalyzed intermolecular hydroaminationCondensation reactionsPreparation of cyclin-dependent kinase inhibitors selective for multiple cyclin-dependent kinases for potential use as antitumor agentsPreparation of hydroxyurea derivatives as small molecule bradykinin B1 receptor antagonists

Technology Process of N-Cyclohexylhydroxylamine

There total 18 articles about N-Cyclohexylhydroxylamine 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: 95.0%