24589-93-3 Usage
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.
Uses
Used in Pharmaceutical Research:
(2-formyl-4-methoxyphenoxy)acetic acid is used as a pharmaceutical candidate for its potential anti-inflammatory and antispasmodic properties, making it a promising agent for the development of new drugs.
Used in Organic Synthesis:
(2-formyl-4-methoxyphenoxy)acetic acid is used as a building block in organic synthesis for its ability to form polymers and contribute to the creation of various chemical compounds.
Used in Research and Development:
(2-formyl-4-methoxyphenoxy)acetic acid is used as a research compound to explore its potential applications and properties in different fields, including its potential use in the development of new materials and pharmaceuticals.
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.
24589-93-3Relevant 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.