59007-06-6

Usage

Uses

Used in Pharmaceutical Applications:
[1,1-Biphenyl]-2,5-diol,3-chloro-(9CI) is used as a pharmaceutical compound for its antioxidant and anti-inflammatory properties, which can contribute to the development of new medications for various health conditions.
Used in Skincare Products:
In the cosmetics industry, [1,1-Biphenyl]-2,5-diol,3-chloro-(9CI) is used as an ingredient in skincare products for its ability to protect against oxidative stress and potentially reduce the appearance of skin aging.
Used in Anticancer Research:
[1,1-Biphenyl]-2,5-diol,3-chloro-(9CI) is used as a compound in anticancer research for its potential anti-cancer properties, making it an interesting candidate for further research and development in the field of oncology.

Upstream product

• 75552-46-4 2-(3'-chlorophenyl)-1,4-benzoquinone 

Relevant academic research and scientific papers

Mechanism of the Oxidation of NADH by Quinones. Energetics of One-Electron and Hydride Routes

The kinetics of NADH oxidation by 7 o-benzoquinones and 14 p-benzoquinones were studied by using buffered aqueous solutions and UV/vis spectroscopy.For each quinone the rate law was first order in NADH and first order in quinone.The rate constants varied from 0.0745 to 9220 M-1s-1.Variation of the pH from 6 to 8 gave no change in rate.The use of 4-D and 4,4-D2NADH revealed kinetic isotope effects.The dideutero data gave kH/kD in the range 1.6-3.1 for p-quinones and 4.2 for 3,5-di-tert-butyl-o-quinone.When p-quinones were used, the log k was a linear function of Eo for the quinone/hydroquinone monoanion (Q/QH(1-)) couple with a slope of 16.9 V-1. o-Quinones reacted about 100 times more rapidly, but the same linear relationship with a slope of 16.4 V-1 was observed.Comparisons to data for one-electron-transfer reactions indicate that such mechanisms are not involved.A hydride-transfer mechanism accommodates all the data, and rate-limiting hydrogen atom transfer followed by electron transfer cannot be ruled out.