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24589-93-3

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24589-93-3 Usage

General Description

(2-formyl-4-methoxyphenoxy)acetic acid, also known as FMPPA, is a chemical compound with the molecular formula C10H10O5. It is a derivative of phenylacetic acid and is commonly used in organic synthesis and pharmaceutical research. FMPPA is a white solid substance with a melting point of 104-106 °C. It has been studied for its potential anti-inflammatory and antispasmodic properties, making it a promising candidate for the development of new pharmaceutical drugs. Additionally, FMPPA has been investigated for its potential use as a building block in organic synthesis and for its ability to form polymers. Overall, FMPPA is a versatile and valuable chemical compound with diverse potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 24589-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,8 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24589-93:
(7*2)+(6*4)+(5*5)+(4*8)+(3*9)+(2*9)+(1*3)=143
143 % 10 = 3
So 24589-93-3 is a valid CAS Registry Number.

24589-93-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-formyl-4-methoxyphenoxy)acetic acid

1.2 Other means of identification

Product number -
Other names 4-Methoxy-2-formyl-phenoxyessigsaeure

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:24589-93-3 SDS

24589-93-3Relevant articles and documents

Organocatalytic Synthesis of Fused Bicyclic 2,3-Dihydro-1,3,4-oxadiazoles through an Intramolecular Cascade Cyclization

Fugard, Alison J.,Thompson, Bethany K.,Slawin, Alexandra M. Z.,Taylor, James E.,Smith, Andrew D.

supporting information, p. 5824 - 5827 (2015/12/11)

Hydrazone-carboxylic acids undergo intramolecular cyclization in the presence of pivaloyl chloride, iPr2NEt, and catalytic DABCO to form a range of substituted fused tricyclic 2,3-dihydro-1,3,4-oxadiazoles in high yields.

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