58506-24-4 Usage
Uses
Given the limited information available on (2-METHOXY-5-METHYLPHENYL)ACETIC ACID, its uses are not well-defined. However, based on its chemical structure and the properties of similar compounds, potential applications could be explored in the following areas:
Used in Chemical Research:
(2-METHOXY-5-METHYLPHENYL)ACETIC ACID could be used as a research compound for studying the properties and reactions of benzenoids and their derivatives. This could contribute to the development of new synthetic pathways or the discovery of novel chemical reactions.
Used in Toxicological Studies:
Due to the scarcity of information on its toxicity, (2-METHOXY-5-METHYLPHENYL)ACETIC ACID could be employed in toxicological studies to assess its potential effects on biological systems. This could help in understanding its safety profile and guide its potential use in various applications.
Used in Pharmaceutical Development:
Although not explicitly mentioned, the chemical structure of (2-METHOXY-5-METHYLPHENYL)ACETIC ACID suggests that it could potentially be used in the development of pharmaceuticals. Further research would be required to explore its bioactivity and potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 58506-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,0 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58506-24:
(7*5)+(6*8)+(5*5)+(4*0)+(3*6)+(2*2)+(1*4)=134
134 % 10 = 4
So 58506-24-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-7-3-4-9(13-2)8(5-7)6-10(11)12/h3-5H,6H2,1-2H3,(H,11,12)/p-1
58506-24-4Relevant academic research and scientific papers
A Formal Total Synthesis of (±)-1,13-Herbertenediol
Srikrishna, Adusuhilli,Rao, M. Srinivasa
, p. 499 - 503 (2007/10/03)
A formal total synthesis of (±)-1,13-herbertenediol, employing a ring-closing metathesis reaction of the 4-arylhepta-1,6-diene-4-carboxylate 15 as the key reaction, is described. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
Preorganized Macrocyclic Ligands: A Novel Approach to Functionalized Hemispherands via Aromatization
Dijkstra, Pieter J.,Skowronska-Ptasinska, Maria,Reinhoudt, David N.,Hertog, Herman J. den,Eerden, Johan van,et al.
, p. 4913 - 4921 (2007/10/02)
Reaction of the 1,3-diaryl-2-propanone moiety in the flexible 18-membered macrocycle 2b with nitromalonodialdehyde to yield the hemispherand 1f represents a novel method for the synthesis of partly preorganized macrocyclic ligands.The O-O repulsion in mac
