N-CYCLOHEXYLHYDROXYLAMINE

N-CYCLOHEXYLHYDROXYLAMINE Basic information
Product Name:N-CYCLOHEXYLHYDROXYLAMINE
Synonyms:Cyclohexylhydroxylamine (CyHHA);n-cyclohexyl-hydroxylamin;cyclohexylhydroxylamine;N-CYCLOHEXYHYDROXYLAMINE;N-Hydroxycyclohexanamine;Hydroxyaminocyclohexane;N-Hydroxycyclohexylamine;Cyclohexanamine, N-hydroxy-
CAS:2211-64-5
MF:C6H13NO
MW:115.17
EINECS:218-650-0
Product Categories:Building Blocks;Chemical Synthesis;Hydroxylamines;Nitrogen Compounds;Nitrogen Compounds;Organic Building Blocks;Organic Building Blocks
Mol File:2211-64-5.mol
N-CYCLOHEXYLHYDROXYLAMINE Structure
N-CYCLOHEXYLHYDROXYLAMINE Chemical Properties
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
pka14.14±0.20(Predicted)
Safety Information
Hazard Codes Xn
Risk Statements 22-41
Safety Statements 26-39
WGK Germany 2
RTECS NC3410400
HS Code 2928009090
MSDS Information
N-CYCLOHEXYLHYDROXYLAMINE Usage And Synthesis
UsesN-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.
UsesReactant 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 DescriptionN-Cyclohexylhydroxylamine is formed as one of the by-products during the hydrogenation of nitrocyclohexane to the corresponding cyclohexanone oxime catalyzed by palladium/carbon nanotubes.
N-CYCLOHEXYLHYDROXYLAMINE Preparation Products And Raw materials
Preparation ProductsCyclamic acid
5-(2-([3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]AMINO)ETHYL)-3,3-SPIRO-2-(5,5-DIMETHYL CYCLOHEXANE-1,3-DIONYL)DIHYDRO-2H-PYRROLO[3,4-D]ISOXAZOLE-4,6-(3H,5H)-DIONE N-CYCLOHEXYLHYDROXYLAMINE (+)-(8,8-DICHLOROCAMPHORYLSULFONYL)OXAZIRIDINE 4-METHYL-2H-IMIDAZOLE-1-OXIDE-2-SPIROCYCLOHEXANE 3-DOXYL-5ALPHA-CHOLESTANE, FREE RADICAL (1S)-(+)-(Camphorylsulfonyl)oxaziridine 2-(HYDROXYAMINO)-2-METHYLCYCLOHEXAN-1-ONE HYDROCHLORIDE 5-NITROSPIRO[BENZIMIDAZOLE-2,1'-CYCLOHEXAN]-4-AMINE 1,3-DIOXIDE 2-(HYDROXYAMINO)CYCLOHEXAN-1-ONE OXIME ACETATE AKOS BB-9950 2,3,5,6-TETRAHYDROXY-1,4-DINITROCYCLOHEXANE DIHYDRATE STRYCHNINE-N-OXIDE 1,2-BIS(HYDROXYAMINO)CYCLOHEXANE N-CYCLOHEXYLHYDROXYLAMINE HYDROCHLORIDE 2-(HYDROXYAMINO)-2-METHYLCYCLOHEXAN-1-ONE OXIME ACETATE 2-NITROCYCLOHEXANONE 1,3-DIHYDROXY-2-CARBOXYPERHYDROBENZIMIDAZOLE ETHANOLATE (1R)-(-)-(10-Camphorsulfonyl)oxaziridine

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