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2-(morpholin-4-yl)ethyl phenylcarbamate is a chemical compound that belongs to the group of phenylcarbamate derivatives. It is characterized by a phenyl ring attached to a carbamate group, which is connected to a morpholine ring via an ethyl chain. 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.

6329-03-9

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6329-03-9 Usage

Uses

Used in Pharmaceutical Industry:
2-(morpholin-4-yl)ethyl phenylcarbamate is used as an intermediate in the synthesis of pharmaceutical products. Its chemical structure allows for the creation of various drug molecules, contributing to the development of new therapeutic agents.
Used in Agrochemical Industry:
2-(morpholin-4-yl)ethyl phenylcarbamate is used as an intermediate in the synthesis of agrochemicals. Its properties make it suitable for the development of compounds that can be used in agricultural applications, such as pesticides or herbicides.
Used in Biological Research:
2-(morpholin-4-yl)ethyl phenylcarbamate is used as a compound of interest in biological research due to its potential anti-tumor and anti-inflammatory properties. Studies on 2-(morpholin-4-yl)ethyl phenylcarbamate may lead to the discovery of new treatments for various diseases and conditions.
Used in Chemical Applications:
2-(morpholin-4-yl)ethyl phenylcarbamate is used as a building block in various chemical applications. Its low toxicity and high stability make it an attractive component for the synthesis of other compounds and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 6329-03-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6329-03:
(6*6)+(5*3)+(4*2)+(3*9)+(2*0)+(1*3)=89
89 % 10 = 9
So 6329-03-9 is a valid CAS Registry Number.

6329-03-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-morpholin-4-ylethyl N-phenylcarbamate

1.2 Other means of identification

Product number -
Other names 2-morpholinoethyl N-phenylcarbamate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6329-03-9 SDS

6329-03-9Downstream Products

6329-03-9Relevant academic research and scientific papers

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

Merino, Daniel Hermida,Feula, Antonio,Melia, Kelly,Slark, Andrew T.,Giannakopoulos, Ioannis,Siviour, Clive R.,Buckley, C. Paul,Greenland, Barnaby W.,Liu, Dan,Gan, Yu,Harris, Peter J.,Chippindale, Ann M.,Hamley, Ian W.,Hayes, Wayne

, p. 368 - 378 (2016)

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

Kinetics of acetonitrile-assisted oxidation of tertiary amines by hydrogen peroxide

Laus

, p. 864 - 868 (2007/10/03)

The rate of oxidation of tertiary amines by aqueous hydrogen peroxide is increased in the presence of acetonitrile due to the formation of a reactive intermediate. The active oxidant, presumably peroxyacetimidic acid, was quantified by a photometric method. Activation parameters of the acetonitrile-assisted and non-assisted oxidations are given in the temperature range 20 to 40 °C. The increased rate of the assisted oxidation is explained by the low enthalpy of activation although the entropy of activation is more negative due to a highly ordered transition state.

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

Dalimov, D. N.,Karimov, D. T.,Vaizburg, G. N.,Abduvakhabov, A. A.,Abdullaeva, L. K.,Kamaev, F. G.

, p. 702 - 708 (2007/10/02)

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

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