34105-76-5 Usage
Description
3,6-Di-tert-butyl-1,2-benzoquinone, also known as 3,6-Di-tert-butyl-o-benzoquinone, is an Ortho-Quinone derivative that exhibits a range of biological properties, including antitumoral, antimicrobial, and anti-cardiovascular disease activities. Its molecular structure, featuring two tert-butyl groups at the 3 and 6 positions, contributes to its diverse applications in various industries.
Uses
Used in Pharmaceutical Industry:
3,6-Di-tert-butyl-1,2-benzoquinone is used as an active pharmaceutical ingredient for its antitumoral properties. It targets and inhibits the growth of cancer cells, making it a potential candidate for the development of new cancer treatments.
Used in Antimicrobial Applications:
In the field of microbiology, 3,6-Di-tert-butyl-1,2-benzoquinone is used as an antimicrobial agent to combat bacterial and fungal infections. Its ability to disrupt cellular processes in microorganisms makes it a valuable asset in the development of new antimicrobial drugs and treatments.
Used in Cardiovascular Disease Prevention:
3,6-Di-tert-butyl-1,2-benzoquinone is used as a preventive agent for cardiovascular diseases. Its anti-inflammatory and antioxidant properties help protect the heart and blood vessels from damage, reducing the risk of heart attacks, strokes, and other cardiovascular conditions.
Used in Cosmetics Industry:
In the cosmetics industry, 3,6-Di-tert-butyl-1,2-benzoquinone is used as an ingredient in various skincare and beauty products due to its antioxidant and antimicrobial properties. It helps maintain the freshness and longevity of products while also providing potential skin health benefits.
Used in Agricultural Industry:
3,6-Di-tert-butyl-1,2-benzoquinone is used as a biopesticide in the agricultural industry. Its antimicrobial properties help protect crops from bacterial and fungal infections, ensuring a healthy and productive yield.
Check Digit Verification of cas no
The CAS Registry Mumber 34105-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,0 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34105-76:
(7*3)+(6*4)+(5*1)+(4*0)+(3*5)+(2*7)+(1*6)=85
85 % 10 = 5
So 34105-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O2/c1-13(2,3)9-7-8-10(14(4,5)6)12(16)11(9)15/h7-8H,1-6H3
34105-76-5Relevant articles and documents
REACTION OF 3,6-DI-TERT-BUTYLPYROCATECHOL WITH THIONYL CHLORIDE IN THE PRESENCE OF DIMETHYLFORMAMIDE
Vol'eva, V. B.,Komissarova, N. L.,Belostotskaya, I. S.,Ershov, V. V.
, p. 1500 - 1502 (1984)
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Intramolecular London Dispersion Interactions Do Not Cancel in Solution
Schümann, Jan M.,Wagner, J. Philipp,Eckhardt, André K.,Quanz, Henrik,Schreiner, Peter R.
, p. 41 - 45 (2021/01/13)
We present a comprehensive experimental study of a di-t-butyl-substituted cyclooctatetraene-based molecular balance to measure the effect of 16 different solvents on the equilibrium of folded versus unfolded isomers. In the folded 1,6-isomer, the two t-bu
Solid-phase oxidation of 2,4-di-tert-butylphenol and 3,6-di-tert-butylpyrocatechol in the presence of alkali and alkaline earth metal halides under elastic deformation
Vol'eva,Prokof'ev,Belostotskaya,Karmilov,Komissarova,Prokof'eva,Ershov
, p. 847 - 850 (2007/10/03)
Solid-phase oxidation of 2,4-di-tert-butylphenol to give 2,2′,4,4′-tert-butyl-6,6′-bisphenol and of 3,6-di-tert-butylpyrocatechol to afford 3,6-di-tert-butyl-1,2-benzoquinone was performed in the presence of alkali and alkaline earth metals halides under conditions of modified extrusion. The formation of the corresponding metal 3,6-di-tert-butylsemiquinolates was registered by ESR method. The different behavior of chlorides, bromides, and iodides was observed and rationalized basing on the dissimilar complexing ability of halogens. The mechanism of activated oxidation was assumed.