24589-92-2 Usage
Derivative of acetic acid
2-(2-formyl-6-methylphenoxy)acetic acid is derived from acetic acid, which means it is a modified version of the parent compound, acetic acid.
Formyl group
The presence of a formyl group (-CHO) in the compound indicates the presence of an aldehyde functional group, which is an important feature for its reactivity and potential applications in organic synthesis.
Phenoxy group
The compound also contains a phenoxy group (C6H4O-), which is an ether functional group derived from a phenol. This group contributes to the compound's stability and reactivity.
Potential applications in organic synthesis
Due to its unique structure and functional groups, 2-(2-formyl-6-methylphenoxy)acetic acid can be used as a building block or intermediate in the synthesis of more complex organic compounds.
Medicinal chemistry applications
The compound's structure and properties make it suitable for use in the development of pharmaceuticals and other bioactive molecules, which could have potential therapeutic benefits.
Industrial uses
Further research and study of 2-(2-formyl-6-methylphenoxy)acetic acid could reveal its potential uses and benefits in various industries, such as the development of new materials or chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 24589-92-2 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 24589-92:
(7*2)+(6*4)+(5*5)+(4*8)+(3*9)+(2*9)+(1*2)=142
142 % 10 = 2
So 24589-92-2 is a valid CAS Registry Number.
24589-92-2Relevant academic research and scientific papers
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.
CHEMICAL COMPOUNDS
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Page/Page column 29-30, (2008/12/04)
This invention relates to non-steroidal compounds that are modulators of androgen receptor, and also to the methods for the making and use of such compounds.
