3088-05-9

Usage

Molecular structure

A complex structure containing a phenyl-amino group, a phenoxy group, and a hydroxy group, as well as a propyl and propan-2-ol backbone.

Functional groups

Contains phenyl-amino, phenoxy, and hydroxy functional groups.

Backbone

Consists of a propyl and propan-2-ol backbone.

Potential applications

Has potential applications in pharmaceuticals and biochemistry due to its unique structure and properties.

Synthesis

May be used in the synthesis of drugs.

Research tool

Could be used as a research tool in the study of biological processes.

Further research

The compound's specific properties and potential uses would need to be further researched and characterized.

Molecular weight

Approximately 409.5 g/mol (calculated from the chemical formula)

Solubility

The solubility of 1-[(2-hydroxy-3-phenoxy-propyl)-phenyl-amino]-3-phenoxy-propan-2-ol is not provided in the material, but it can be inferred that it may be soluble in organic solvents due to the presence of hydrophobic groups (phenyl and propyl).

Stability

The stability of the compound is not mentioned in the material, but it may be sensitive to certain conditions such as heat, light, or acidic/basic environments, which could affect its reactivity or degradation.

Reactivity

The reactivity of the compound is not provided in the material, but the presence of multiple functional groups suggests that it may undergo various chemical reactions, such as substitution, addition, or elimination reactions.

Purity

The purity of the compound is not mentioned in the material, but it is an important factor to consider when evaluating its potential applications and properties.

Safety

The safety profile of the compound is not provided in the material, but it is crucial to assess its toxicity, mutagenicity, and other potential hazards before using it in pharmaceuticals or research applications.

Upstream product

• 122-60-1 Phenyl glycidyl ether 
• 62-53-3 aniline 

Relevant academic research and scientific papers

Thermokinetics of the reaction of phenyl glycidyl ether with aniline

The thermokinetic curves in the reaction of phenyl glycidyl ether with aniline were calculated for various compositions of the reaction mixture and temperatures. In addition to the main exothermic effect related to the epoxide ring opening, another exothermic effect of unknown nature was observed. The kinetic data obtained are explained in terms of structural changes caused by the self-aggregation of the reaction product molecules. The "kinetic investigation" approach provides a quantitative analysis of calorimetric data.

A Multicomponent Approach to Oxazolidinone Synthesis Catalyzed by Rare-Earth Metal Amides

Three-component reaction of epoxides, amines, and dimethyl carbonate catalyzed by rare-earth metal amides has been developed to synthesize oxazolidinones. 47 examples of 3,5-disubstituted oxazolidinones were prepared in 13–97 % yields. This is a simple and most practical method which employs easily available substrates and catalysts, and is applicable to a wide range of aromatic and aliphatic amines, as well as mono-substituted epoxides. Scope of disubstituted epoxides is rather limited, which requires further study. Preliminary mechanistic study reveals two possible reaction pathways through intermediates of β-amino alcohols or amides.

CONTINUOUS FLOW SYNTHESIS OF AMINO ALCOHOLS USING MICROREACTORS

The present invention provides various methods for the synthesis of chemical species in a microreactor environment. In some cases, reaction products of the present invention may be valuable as intermediates and/or products in pharmaceutical and polymer research. For example, the method may involve the synthesis of amino alcohols within a microchannel. Embodiment described herein may allow for reactions with significantly shorter reaction times and increased efficiency.

Aminolysis of epoxides in a microreactor system: A continuous flow approach to β-Amino alcohols

The use of a continuous flow microreactor for β-amino alcohol formation by epoxide aminolysis is evaluated. Comparison to microwave batch reactions reveals that conditions obtainable in the microreactor can match or improve yields in many cases. By increasing the pressure of the system, maximum temperatures can also exceed those accessible using a microwave unit. The use of a microreactor for epoxide aminolysis reactions in the synthesis of two pharmaceutical relevant compounds is described.