6329-03-9

Basic information

• Product Name: 2-(morpholin-4-yl)ethyl phenylcarbamate
• Synonyms: 2-morpholinoethyl phenylcarbamate
• CAS NO: 6329-03-9
• Molecular Formula: C₁₃H₁₈N₂O₃
• Molecular Weight: 250.2936
• Mol File: 6329-03-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 348.7°C at 760 mmHg
• Flash Point: 164.7°C
• Density: 1.192g/cm³
• Vapor Pressure: 4.95E-05mmHg at 25°C
• Refractive Index: 1.566
• CAS DataBase Reference: 2-(morpholin-4-yl)ethyl phenylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(morpholin-4-yl)ethyl phenylcarbamate(6329-03-9)
• EPA Substance Registry System: 2-(morpholin-4-yl)ethyl phenylcarbamate(6329-03-9)

Safety Data

• Hazardous Substances Data: 6329-03-9(Hazardous Substances Data)

Usage

General Description

2-(morpholin-4-yl)ethyl phenylcarbamate is a chemical compound that belongs to the group of phenylcarbamate derivatives. It consists of a phenyl ring attached to a carbamate group, which is in turn connected to a morpholine ring via an ethyl chain. 2-(morpholin-4-yl)ethyl phenylcarbamate is commonly used as an intermediate in the synthesis of pharmaceutical products and agrochemicals. It has also been studied for its potential biological activities, including anti-tumor and anti-inflammatory properties. Additionally, 2-(morpholin-4-yl)ethyl phenylcarbamate is known for its low toxicity and high stability, making it a valuable building block in various chemical and pharmaceutical applications.

Upstream product

• 622-40-2 2-(morpholin-4-yl)ethanol 
• 103-71-9 phenyl isocyanate 

Relevant articles and documents

A systematic study of the effect of the hard end-group composition on the microphase separation, thermal and mechanical properties of supramolecular polyurethanes

This paper reports a systematic study on a series of supramolecular polyurethanes that possess microphase separated morphologies which afford elastic materials at room temperature. Combinations of urea and/or urethane linkers in addition to a phenyl space

SYNTHESIS OF A NUMBER OF DERIVATIVES OF ALKALOIDS AND OF NITROGEN-CONTAINING HETEROCYCLES AND THEIR ANTICHOLINESTERASE ACTIVITIES

N-Methyl- and N-phenylcarbamates based on a number of alkaloids and nitrogen-containing heterocycles have been synthesized, and they have proved to be weak irreversible inhibitors of acetylcholinesterase and butyrylcholinesterase.It has been shown that th