167627-21-6 Usage
Uses
Used in Pharmaceutical Synthesis:
[1,1-Biphenyl]-4-carboxylic acid,2,6-dihydroxy-(9CI) is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Synthesis:
[1,1-Biphenyl]-4-carboxylicacid,2,6-dihydroxy-(9CI) is also employed in the synthesis of agrochemicals, contributing to the development of new products for the agricultural industry.
Used in Antioxidant Applications:
Due to its antioxidant properties, [1,1-Biphenyl]-4-carboxylic acid,2,6-dihydroxy-(9CI) can be used as an additive in the food and cosmetic industries to extend shelf life and protect against oxidative damage.
Used in Anti-inflammatory Applications:
Its anti-inflammatory properties make [1,1-Biphenyl]-4-carboxylic acid,2,6-dihydroxy-(9CI) a potential candidate for the development of new anti-inflammatory drugs, which could be used to treat various inflammatory conditions.
Used in Disease Treatment Research:
Further research is being conducted to explore the potential of [1,1-Biphenyl]-4-carboxylic acid,2,6-dihydroxy-(9CI) in the treatment of various diseases, highlighting its versatility and potential impact on the field of medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 167627-21-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,6,2 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 167627-21:
(8*1)+(7*6)+(6*7)+(5*6)+(4*2)+(3*7)+(2*2)+(1*1)=156
156 % 10 = 6
So 167627-21-6 is a valid CAS Registry Number.
167627-21-6Relevant articles and documents
Tunable Artificial Enzyme-Cofactor Complex for Selective Hydrolysis of Acetals
Bose, Ishani,Fa, Shixin,Zhao, Yan
, p. 1701 - 1711 (2021)
Enzymes frequently use unimpressive functional groups such as weak carboxylic acids for efficient, highly selective catalysis including hydrolysis of acetals and even amides. Much stronger acids generally have to be used for such purposes in synthetic systems. We report here a method to position an acidic group near the acetal oxygen of 2-(4-nitrophenyl)-1,3-dioxolane bound by an artificial enzyme. The hydrolytic activity of the resulting artificial enzyme-cofactor complex was tuned by the number and depth of the active site as well as the hydrophobicity and acidity of the cofactor. The selectivity of the complex was controlled by the size and shape of the active site and enabled less reactive acetals to be hydrolyzed over more reactive ones.
