75066-24-9 Usage
Uses
Used in Pharmaceutical Industry:
2-(3,4-DIMETHYL-PHENOXY)-2-METHYL-PROPIONIC ACID is used as a building block for the synthesis of various pharmaceuticals. Its ability to inhibit the production of pro-inflammatory mediators makes it a valuable component in the development of anti-inflammatory and analgesic medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(3,4-DIMETHYL-PHENOXY)-2-METHYL-PROPIONIC ACID serves as a key intermediate in the creation of agrochemicals, potentially contributing to the development of new pesticides or other agricultural chemicals that can enhance crop protection and yield.
Used in Neurological Disorder Treatment:
2-(3,4-DIMETHYL-PHENOXY)-2-METHYL-PROPIONIC ACID is being studied for its potential application in the treatment of neurological disorders. Its specific mechanisms and efficacy in this area are under investigation, but the compound's bioactivity suggests it may offer therapeutic benefits.
Used in Anticancer Research:
2-(3,4-DIMETHYL-PHENOXY)-2-METHYL-PROPIONIC ACID is also being explored for its potential as an anticancer agent. While further research is needed to understand its full capabilities and mechanisms in this context, the study of 2-(3,4-DIMETHYL-PHENOXY)-2-METHYL-PROPIONIC ACID in cancer treatment is a promising avenue for future pharmaceutical development.
Check Digit Verification of cas no
The CAS Registry Mumber 75066-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,6 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75066-24:
(7*7)+(6*5)+(5*0)+(4*6)+(3*6)+(2*2)+(1*4)=129
129 % 10 = 9
So 75066-24-9 is a valid CAS Registry Number.
75066-24-9Relevant academic research and scientific papers
The Synthesis of 4-Methylcyclohexa-2,5-dienones from Phenols
Islam, M. Majharul,Waring, Anthony J.
, p. 768 - 783 (2007/10/02)
4-Alkyl phenols have been converted by a known sequence into 2-aryloxyisobutyric acids and thence, by bromination at the 4-position of the aromatic ring with concomitant intramolecular lactone formation, into masked 4-alkyl-4-bromocyclohexa-2,5-dienones.Reaction with lithium dimethylcuprate, as a model for other lithium dialkylcuprates, replaces the bromine by a methyl group.Hydrolytic demasking gives 4-alkyl-4-methylcyclohexa-2,5-dienones.The method should allow the general synthesis of 4-alkylated cyclohexa-2,5-dienones from phenols via a nucleophilic alkylation step.This contrasts with an existing route which uses electrophilic alkylation of phenols or phenoxide ions by a restricted range of reactive alkylating agents.
