ChemicalBook Product Catalog Chemical Reagents Organic reagents Hydroxylamine N-Benzylhydroxylamine hydrochloride

N-Benzylhydroxylamine hydrochloride

N-Benzylhydroxylamine hydrochloride Basic information
Product Name:N-Benzylhydroxylamine hydrochloride
Synonyms:N-hydroxy-BenzeneMethanaMine hydrochloride;N-Benzylhydroxylamine hydrochloride 97%;BenzeneMethanaMine,N-hydroxy-, hydrochloride (1:1);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);N-BENZYLHYDROXYLAMINE HYDROCHLORIDE;Benzenemethanamine, N-hydroxy-, hydrochloride;Benzyl(hydroxy)ammonium chloride
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 Structure
N-Benzylhydroxylamine hydrochloride Chemical Properties
Melting point 108-110 °C(lit.)
storage temp. Inert atmosphere,Room Temperature
solubility DMSO (Slightly), Ethyl Acetate (Slightly, Heated), Methanol (Slightly)
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
F 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.
2-(2-CHLOROETHYL)-4-OXO-3,4-DIHYDRO-2H-1,3-BENZOXAZIN-3-YL N-(4-CHLOROPHENYL)CARBAMATE N-Benzylhydroxylamine hydrochloride N,N-BIS(2-CHLORO-6-FLUOROBENZYL)-N-(([(1,2,2-TRICHLOROVINYL)AMINO]CARBONYL)OXY)AMINE 2-(2-CHLOROETHYL)-4-OXO-3,4-DIHYDRO-2H-1,3-BENZOXAZIN-3-YL N-PHENYLCARBAMATE Topotecan hydrochloride N-BENZYLHYDROXYLAMINE HYDROCHLORIDE Phenylacetone N-[(2-CHLOROACETYL)OXY]-N,N-BIS(4-CHLOROBENZYL)AMINE N,N-BIS(2-CHLORO-6-FLUOROBENZYL)-N-(([(2,2-DICHLOROETHANIMIDOYL)AMINO]CARBONYL)OXY)AMINE 2-(2-CHLOROETHYL)-4-OXO-3,4-DIHYDRO-2H-1,3-BENZOXAZIN-3-YL 2-CHLOROBENZOATE N-[(2,4-DICHLOROBENZYL)OXY]-2,5-BIS(2,2,2-TRIFLUOROETHOXY)BENZENECARBOXAMIDE [AMINO(4-CHLOROPHENYL)METHYLIDENE][2-(CHLOROMETHYL)BENZOYL]AMMONIUMOLATE 2-[(2-CHLORO-6-FLUOROBENZYL)OXY]-1H-ISOINDOLE-1,3(2H)-DIONE 3-(5-CHLORO-2-HYDROXYPHENYL)-3-METHYL-2,3,5,6,7,8-HEXAHYDRO-1,2,4-BENZOTRIAZIN-4-IUM-4-OLATE 2-(2-CHLOROETHYL)-4-OXO-3,4-DIHYDRO-2H-1,3-BENZOXAZIN-3-YL 4-CHLOROBENZOATE 4-AMINO-6-CHLORO-2-(4-METHYLPHENYL)-1,2-DIHYDROQUINAZOLIN-3-IUM-3-OLATE [AMINO(4-CHLOROPHENYL)METHYLIDENE][3-(CHLOROMETHYL)BENZOYL]AMMONIUMOLATE N,N-BIS(2-CHLORO-6-FLUOROBENZYL)HYDROXYLAMINE
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