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β-(4-hydroxy-3-methylphenyl)butyric acid, also known as 3-methyl-4-hydroxyphenylbutyric acid, is a naturally occurring organic compound with the chemical formula C11H14O4. It is a derivative of hydroxyphenylbutyric acid, featuring a 4-hydroxy-3-methylphenyl group attached to a butyric acid chain. β-(4-hydroxy-3-methylphenyl)butyric acid is known for its potential neuroprotective properties and has been studied for its role in the treatment of neurological disorders such as Huntington's disease. It works by inhibiting the enzyme glutathione S-transferase, which is involved in the breakdown of the neurotransmitter glutamate, thus potentially reducing excitotoxicity in the brain. The compound's structure and activity make it a subject of interest in pharmaceutical research for its potential therapeutic applications.

24552-31-6

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24552-31-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24552-31-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,5 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24552-31:
(7*2)+(6*4)+(5*5)+(4*5)+(3*2)+(2*3)+(1*1)=96
96 % 10 = 6
So 24552-31-6 is a valid CAS Registry Number.

24552-31-6Downstream Products

24552-31-6Relevant academic research and scientific papers

CARBOXYALKYLATION OF ISOMERIC CRESOLS BY THE FRIEDEL-CRAFTS REACTION

Barashkin, V. A.,Kadyrov, Ch. Sh.

, p. 915 - 920 (2007/10/02)

The condensation of isomeric cresols with γ-butyrolactone and β-chlorobutyric acid in the presence of an excess of aluminum chloride leads to mixtures of isomeric β-cresylbutyric acids.The use of tetrachloroethylene as solvent in these reactions affects not only the yield but also the isomeric composition of the reaction products.

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