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Morpholin-3-yl-acetic acid ethyl ester, with the molecular formula C10H19NO3, is a versatile chemical compound derived from morpholine. It serves as a crucial intermediate in the synthesis of pharmaceuticals and agrochemicals, and also functions as a building block in organic synthesis. Additionally, it is recognized for its role as a stabilizer in plastic and rubber materials, showcasing its broad applications across various fields in chemistry and industry.

81684-84-6

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81684-84-6 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
Morpholin-3-yl-acetic acid ethyl ester is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows it to be incorporated into the development of new drugs and pesticides, contributing to advancements in healthcare and agriculture.
Used in Organic Synthesis:
As a building block in organic synthesis, Morpholin-3-yl-acetic acid ethyl ester is utilized for the creation of a wide range of organic compounds. Its versatility enables chemists to explore new chemical pathways and synthesize novel molecules with potential applications in various industries.
Used in Plastic and Rubber Industries:
Morpholin-3-yl-acetic acid ethyl ester is employed as a stabilizer in the production of plastic and rubber materials. Its ability to enhance the stability and durability of these materials makes it an essential component in the manufacturing process, ensuring the longevity and performance of the final products.

Check Digit Verification of cas no

The CAS Registry Mumber 81684-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,8 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81684-84:
(7*8)+(6*1)+(5*6)+(4*8)+(3*4)+(2*8)+(1*4)=156
156 % 10 = 6
So 81684-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO3/c1-2-12-8(10)5-7-6-11-4-3-9-7/h7,9H,2-6H2,1H3

81684-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-morpholin-3-ylacetate

1.2 Other means of identification

Product number -
Other names ETHYL3-MORPHOLINYLACETATE

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:81684-84-6 SDS

81684-84-6Relevant academic research and scientific papers

SUBSTITUTED MORPHOLINES AS MODULATORS FOR THE CALCIUM SENSING RECEPTOR

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Paragraph 0380, (2014/02/15)

Compounds of Formula (I) along with processes for their preparation that are useful for treating, managing and/or lessening the diseases, disorders, syndromes or conditions associated with the modulation of calcium sensing (CaSR) receptors. Methods of treating, managing and/or lessening the diseases, disorders, syndromes or conditions associated with the modulation of calcium sensing (CaSR) receptors of Formula (I).

SUBSTITUTED MORPHOLINES AS MODULATORS FOR THE CALCIUM SENSING RECEPTOR

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Page/Page column 65, (2012/09/22)

Compounds of Formula (I) along with processes for their preparation that are useful for treating, managing and/or lessening the diseases, disorders, syndromes or conditions associated with the modulation of calcium sensing (Ca SR) receptors. Methods of treating, managing and/or lessening the diseases, disorders, syndromes or conditions associated with the modulation of calcium sensing (Ca SR) receptors of Formula (I).

Decarboxylation Reaction. X. Introduction of a Carbon unit at the α-Position of Amines by Reaction of Hexahydro-1,3,5-triazines with Carboxylic Acids

Fukawa, Hidemichi,Terao, Yoshiyasu,Achiwa, Kazuo,Sehiya, Minoru

, p. 94 - 99 (2007/10/02)

An efficient method for introducing a carbon unit at the α-position of alicyclic amines is described.The method involves the reaction of monocyclic or tetracyclic hexahydro-1,3,5-triazines with trichloroacetic acid, cyanoacetic acid, malonic acid and their derivatives, which are introduced into the α-position of amines in the decarboxylated form.Keywords --- 1,3,5-trialkylhexahydro-1,3,5-triazine; trimer of alicyclic imine; decarboxylation; β-amino acid; carboxylic acid

INTRODUCTION OF CARBON UNIT AT THE α-POSITION OF ALICYCLIC AMINES UTILIZING A DECARBOXYLATION REACTION WITH MALONIC ACID DERIVATIVES

Fukawa, Hidemichi,Terao, Yoshiyasu,Achiwa, Kazuo,Sekiya, Minoru

, p. 231 - 232 (2007/10/02)

A new method for introducing carbon unit at the α-position of alicyclic amines has been exploited.The method involves a reaction of trimers of alicyclic imines with malonic acid derivatives, of which decarboxylation leads to a formation of carbon-carbon bond at the α-position of alicyclic amines.

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