13571-04-5

Basic information

• Product Name: O-Phenethyl-hydroxylamine hydrochloride
• Synonyms: O-Phenethyl-hydroxylamine hydrochloride;AMINOOXYPROPANE HYDROCHLORIDE;O-AMino-2-phenylethanol hydrochloride
• CAS NO: 13571-04-5
• Molecular Formula: C8H12ClNO
• Molecular Weight: 173.63998
• Mol File: 13571-04-5.mol
• Article Data: 5

Chemical Properties

• Melting Point: 101 °C
• Boiling Point: 259°Cat760mmHg
• Flash Point: 124.2°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.0133mmHg at 25°C
• CAS DataBase Reference: O-Phenethyl-hydroxylamine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: O-Phenethyl-hydroxylamine hydrochloride(13571-04-5)
• EPA Substance Registry System: O-Phenethyl-hydroxylamine hydrochloride(13571-04-5)

Safety Data

• Hazardous Substances Data: 13571-04-5(Hazardous Substances Data)

Usage

General Description

O-Phenethyl-hydroxylamine hydrochloride is a chemical compound that consists of a hydroxylamine group attached to a phenethyl group, with a chloride ion. O-Phenethyl-hydroxylamine hydrochloride is used in organic synthesis as a reagent for the formation of oximes and hydrazones. It is also used in the pharmaceutical industry for the synthesis of certain drugs. O-Phenethyl-hydroxylamine hydrochloride is a white to off-white crystalline solid, and it is soluble in water and organic solvents. It is important to handle this compound with caution, as it may pose health hazards if not properly handled and stored.

InChI:InChI=1/C8H11NO.ClH/c9-10-7-6-8-4-2-1-3-5-8;/h1-5H,6-7,9H2;1H

Upstream product

• 4732-11-0 O-(2-phenylethyl)hydroxylamine 
• 103-63-9 1-phenyl-2-bromoethane 

Downstream Products

• 178755-29-8 (E)-N-(2-Phenylethyloxy)iminoacetic acid 
• 1885-50-3 <2-Phenyl-ethoxy>-guanidin 

Relevant articles and documents

Direct cycle between co-product and reactant: An approach to improve the atom economy and its application in the synthesis and protection of primary amines

Two important goals of green chemistry are to maximize the efficiency of reactants and to minimize the production of waste. In this study, a novel approach to improve the atom economy of a chemical process was developed by incorporating a direct cycle between a co-product and a reactant of the same reaction. To demonstrate this concept, recoverable 3,4-diphenylmaleic anhydride (1) was designed and used for the atom-economical synthesis of aliphatic primary amines from aqueous ammonia. In each individual cycle, only ammonia and alkyl halide were consumed, and 1 was recovered in nearly a quantitative yield. In this approach for developing atom-economical protecting agents, 1 showed good performance as a recoverable protecting agent for primary amines. The broad substrate scope, good tolerance to various reaction conditions, and high reaction and recovery rates make 1 a valuable complement to conventional primary amine protecting agents.

CONTROLLED RELEASE OF ACTIVE COMPOUNDS FROM DYNAMIC MIXTURES

The present invention relates to a dynamic mixture in the form of a dynamic mixture obtained by reacting together, in the presence of water, at least one O-substituted hydroxylamine or S-substituted thiohydroxylamine derivative with at least one perfuming

Symmetrical O-substituted dioximes of benzo-fused β-diketocyclo-alkylenes, the processes for their preparation and their application as drugs

Drugs with high anticonvulsant and analgesic activities constituted by symmetrical β-dialkoxyiminocycloalklene derivatives in which the imine double bonds are conjugated with the cyclic double bond or bonds belonging to one or more fused benzene rings. They correspond to the general formula I: STR1