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2211-64-5

2211-64-5 Structure

2211-64-5 Structure
IdentificationBack Directory
[Name]

N-CYCLOHEXYLHYDROXYLAMINE
[CAS]

2211-64-5
[Synonyms]

cyclohexylhydroxylamine
Hydroxyaminocyclohexane
N-Hydroxycyclohexylamine
N-CYCLOHEXYHYDROXYLAMINE
N-Hydroxycyclohexanamine
n-cyclohexyl-hydroxylamin
Cyclohexanamine, N-hydroxy-
Cyclohexylhydroxylamine (CyHHA)
[EINECS(EC#)]

218-650-0
[Molecular Formula]

C6H13NO
[MDL Number]

MFCD00021287
[MOL File]

2211-64-5.mol
[Molecular Weight]

115.17
Chemical PropertiesBack Directory
[Melting point ]

139-140 °C(lit.)
[Boiling point ]

215.49°C (rough estimate)
[density ]

0.9837 (rough estimate)
[refractive index ]

1.4690 (estimate)
[storage temp. ]

-20°C
[form ]

solid
[pka]

14.14±0.20(Predicted)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-41
[Safety Statements ]

26-39
[WGK Germany ]

2
[RTECS ]

NC3410400
[HS Code ]

2928009090
Hazard InformationBack Directory
[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.
[Uses]

Reactant for:
  • Aldehyde-catalyzed intermolecular hydroamination
  • Condensation reactions
  • Preparation of cyclin-dependent kinase inhibitors selective for multiple cyclin-dependent kinases for potential use as antitumor agents
  • Preparation of hydroxyurea derivatives as small molecule bradykinin B1 receptor antagonists
[General Description]

N-Cyclohexylhydroxylamine is formed as one of the by-products during the hydrogenation of nitrocyclohexane to the corresponding cyclohexanone oxime catalyzed by palladium/carbon nanotubes.
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