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3-Ethoxypropionic acid is a colorless liquid organic compound characterized by the chemical formula C5H10O3. It is recognized for its versatility in organic synthesis due to its ability to participate in esterification, acylation, and other organic reactions, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.

4324-38-3

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4324-38-3 Usage

Uses

Used in Pharmaceutical Synthesis:
3-Ethoxypropionic acid is used as a precursor in the pharmaceutical industry for the synthesis of various drugs. Its reactivity with other chemicals allows for the creation of a wide range of medicinal compounds, contributing to the development of new treatments and therapies.
Used in Agrochemical Production:
In the agrochemical sector, 3-Ethoxypropionic acid serves as a key intermediate in the production of pesticides and other agricultural chemicals. Its role in the synthesis of these compounds helps to ensure the development of effective solutions for crop protection and enhancement of agricultural yields.
Used as a Solvent in Industrial Applications:
3-Ethoxypropionic acid is utilized as a solvent in various industries, particularly in the manufacturing of polymers and resins. Its solvent properties facilitate the processing and production of these materials, enhancing their performance and applicability in diverse industrial settings.
Used in Organic Synthesis as a Building Block:
3-Ethoxypropionic acid is employed as a versatile building block in organic synthesis across different chemical industries. Its capacity to undergo various organic reactions makes it an essential component in the creation of complex organic molecules for a multitude of applications.
Safety Considerations:
It is crucial to handle 3-Ethoxypropionic acid with care due to its potential harmful effects if ingested, inhaled, or comes into contact with the skin. Proper safety measures should be implemented during its use to minimize risks and ensure the well-being of individuals involved in its handling and application.

Check Digit Verification of cas no

The CAS Registry Mumber 4324-38-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,2 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4324-38:
(6*4)+(5*3)+(4*2)+(3*4)+(2*3)+(1*8)=73
73 % 10 = 3
So 4324-38-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O3/c1-2-8-4-3-5(6)7/h2-4H2,1H3,(H,6,7)

4324-38-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Ethoxypropionic Acid

1.2 Other means of identification

Product number -
Other names O-ETHYLHYDRACRYLIC ACID

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:4324-38-3 SDS

4324-38-3Relevant articles and documents

Efficient copper-catalyzed Michael addition of acrylic derivatives with primary alcohols in the presence of base

Wang, Feng,Yang, Haijun,Fu, Hua,Pei, Zhichao

supporting information, p. 517 - 519 (2013/02/23)

A novel and efficient copper-catalyzed Michael addition of acrylic derivatives with primary alcohols in the presence of base has been developed. The protocol uses readily available acrylic derivatives and primary alcohols as the starting materials, inexpensive CuCl2 as the catalyst, and the corresponding addition products were obtained in moderate to excellent yields.

Tetrapeptidehydrazide derivatives

-

, (2008/06/13)

Novel tetrapeptidehydrazide derivatives, inclusive of a pharmacologically acceptable acid addition salt thereof, which has the general formula (I): STR1 [wherein R1 is hydrogen or lower alkyl; R2 is hydrogen or the side chain of a D-α-amino acid; R3 is hydrogen or lower alkyl; R4 is hydrogen, or a saturated or unsaturated and straight or branched lower aliphatic acyl group which may optionally be substituted by hydroxy, amino, lower alkoxy, halogen, oxo, lower alkylthio or lower alkylthiooxide], are useful as analgesics.

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