69061-62-7 Usage
Uses
Used in Food Industry:
3-(3-Methoxyphenyl)pentanedioic acid is used as a flavoring agent for its unique taste and aroma, enhancing the flavor profiles of various food products.
Used in Pharmaceutical Industry:
3-(3-Methoxyphenyl)pentanedioic acid is used as a potential medicinal compound for its antioxidant, anti-inflammatory, and anticancer properties. It has been studied for its potential health benefits and may be utilized in the development of new drugs and treatments.
Used in Antioxidant Applications:
3-(3-Methoxyphenyl)pentanedioic acid is used as an antioxidant in various industries, including food, cosmetics, and pharmaceuticals, to protect against oxidative stress and prevent the formation of harmful free radicals.
Used in Anti-Inflammatory Applications:
3-(3-Methoxyphenyl)pentanedioic acid is used as an anti-inflammatory agent, potentially reducing inflammation and alleviating symptoms associated with various inflammatory conditions.
Used in Anticancer Applications:
3-(3-Methoxyphenyl)pentanedioic acid is used as a potential anticancer agent, with studies suggesting its ability to inhibit cancer cell growth and proliferation, making it a promising candidate for further research and development in cancer treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 69061-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,6 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69061-62:
(7*6)+(6*9)+(5*0)+(4*6)+(3*1)+(2*6)+(1*2)=137
137 % 10 = 7
So 69061-62-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O5/c1-17-10-4-2-3-8(5-10)9(6-11(13)14)7-12(15)16/h2-5,9H,6-7H2,1H3,(H,13,14)(H,15,16)
69061-62-7Relevant academic research and scientific papers
Complementary lipase-mediated desymmetrization processes of 3-Aryl-1,5-disubstituted fragments. enantiopure synthetic valuable carboxylic acid derivatives
Rios-Lombardia, Nicolas,Gotor-Fernandez, Vicente,Gotor, Vicente
experimental part, p. 811 - 819 (2011/04/23)
Desymmetrizaton enzymatic processes have been extensively studied searching for optimal methods of producing enantioenriched monoacetates from prochiral diols and diesters. AK lipase has been found as an excellent biocatalyst for the desymmetriaztion of a series of previously synthesized 3-arylpentane-1,5-diols derivatives. The access to (S)- or (R)-monoacetates in high optical purity (86-99% ee) has been possible by using acetylation or hydrolysis reactions, respectively, where the reaction parameters have been optimized in terms of source and amount of biocatalyst, temperature, solvent, and reaction time. The synthetic potential of enantiopure monoesters has been demonstrated by using these interesting chiral building blocks for the preparation of novel enantiopure carboxylic acid derivatives.
