N-Benzylhydroxylamine hydrochloride

N-Benzylhydroxylamine hydrochloride
  • CAS No.:29601-98-7
Other grades of this product :
N-Benzylhydroxylamine hydrochloride Basic information
Product Name:N-Benzylhydroxylamine hydrochloride
Synonyms:N-BENZYLHYDROXYLAMINE HYDROCHLORIDE;Benzenemethanamine, N-hydroxy-, hydrochloride;N-hydroxy-BenzeneMethanaMine hydrochloride;N-Benzylhydroxylamine hydrochloride 97%;BenzeneMethanaMine,N-hydroxy-, hydrochloride (1:1);Benzyl(hydroxy)ammonium chloride;N-benzylhydroxylamine hydrochloride, N-benzyl-N-hydroxylamine hydrochloride, benzyl-hydroxylamine monohydrochloride, benzyl hydroxylamine hydrochloride, o-benzylhydroxyamine hydrochloride, O-benzylhydroxyamine HCl, N-hydroxy-1-phenylmethanamine hydrochloride;N-Benzylhydroxylamine hydrochloride≥ 98%(HPLC)
CAS:29601-98-7
MF:C7H10ClNO
MW:159.61
EINECS:
Product Categories:Hydroxylamines;Nitrogen Compounds;Organic Building Blocks;1
Mol File:29601-98-7.mol
N-Benzylhydroxylamine hydrochloride Chemical Properties
Melting point 108-110 °C(lit.)
storage temp. Inert atmosphere,Room Temperature
form powder to crystal
color White to Light yellow
BRN 507948
InChIKeyYSNXOQGDHGUKCZ-UHFFFAOYSA-N
CAS DataBase Reference29601-98-7
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 3
3-10
HS Code 29280000
MSDS Information
ProviderLanguage
SigmaAldrich English
N-Benzylhydroxylamine hydrochloride Usage And Synthesis
Chemical PropertiesWhite crystalline
UsesN-Benzylhydroxylamine hydrochloride may be used in the preparation of a precursor to hitherto unknown aminocyclopentitol derivative, hydroxy functionalised 4-exo-ethoxycarbonyl-3-oxa-2-azabicyclo[3.3.0]octane system.
General DescriptionN-Benzylhydroxylamine hydrochloride is a N-substituted-hydroxylamine. It participates in the ring opening of (2S,3R)-1,2-epoxy-4-penten-3-ol. Two-step synthesis of N-benzylhydroxylamine starting from dibenzylamine is reported.
Biochem/physiol ActionsN-Benzylhydroxylamine is a potential pharmacological agent in the prevention and progression of acrolein-induced damage to the retinal pigment epithelium.

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