89244-04-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
1,2,4-Benzenetriol, 6-pentylis derived from benzenetriol, which is a type of phenol compound.
Explanation
This is another way to refer to the chemical compound, emphasizing its structure and functional groups.
Explanation
The compound is used in the production of various pharmaceuticals and serves as a starting material for the synthesis of other organic compounds.
Explanation
1,2,4-Benzenetriol, 6-pentylexhibits antioxidant properties, which can be beneficial in various applications, including skincare products.
Explanation
The compound is being studied for its potential use in skincare products and as a possible treatment for certain medical conditions due to its antioxidant properties.
Explanation
1,2,4-Benzenetriol, 6-pentylis being investigated for its potential role in cancer treatment and prevention, which could lead to new therapeutic approaches.
Explanation
The chemical structure of 1,2,4-Benzenetriol, 6-pentylconsists of a benzene ring with three hydroxyl (OH) groups attached and a pentyl (C5H11) chain, which contributes to its unique properties and applications.
Derivative of
Benzenetriol
Applications
Pharmaceutical production, precursor for organic synthesis
Antioxidant properties
Yes
Potential use
Skincare products, medical treatments
Research focus
Cancer treatment and prevention
Chemical structure
Contains a benzene ring with three hydroxyl groups and a pentyl chain
Check Digit Verification of cas no
The CAS Registry Mumber 89244-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,4 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89244-04:
(7*8)+(6*9)+(5*2)+(4*4)+(3*4)+(2*0)+(1*4)=152
152 % 10 = 2
So 89244-04-2 is a valid CAS Registry Number.
89244-04-2Relevant academic research and scientific papers
DNA cleavage by Di- and trihydroxyalkylbenzenes. Characterization of products and the roles of O2, Cu(II), and alkali
Singh, Udai S.,Scannell, Ralph T.,An, Haoyun,Carter, Barbara J.,Hecht, Sidney M.
, p. 12691 - 12699 (2007/10/03)
Several 5-alkyl-1,3-dihydroxybenzene (5-alkylresorcinol, 1) and 6-alkyl-1,2,4-trihydroxybenzene (2) derivatives were prepared and used to study the mechanism by which such compounds effect Cu(II)-dependent DNA strand scission. Comparison of the methyl, n-pentyl, n-undecyl, and n-hexadecyl derivatives in each structural series indicated that the efficiency of DNA cleavage increased with increasing length of the alkyl substituent. DNA cleavage by the 5-alkylresorcinols appears to involve initial oxygenation of the benzene nucleus, a process that occurs readily at alkaline pH in the presence of Cu2+ and O2. The resulting trihydroxylated benzenes mediate DNA cleavage in a reaction dependent on the presence of both Cu2+ and O2. The mechanism appears to involve reduction of Cu2+ by the trihydroxybenzene moiety in 2, with subsequent formation of reactive oxygen species. The ability of catalase and dimethyl sulfoxide to suppress DNA strand scission is consistent with the intermediacy of H2O2 and ?OH in the DNA strand scission process.
