87538-42-9 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
2,4-Dihydroxybenzil is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with therapeutic and pesticidal properties.
Used in Dye Production:
2,4-Dihydroxybenzil is used as a key component in the production of dyes. Its chemical properties enable the creation of a wide range of colors, making it a valuable asset in the dye industry.
Used in Polymer Synthesis:
2,4-Dihydroxybenzil is utilized in the synthesis of polymers due to its reactive hydroxyl groups. These polymers find applications in various fields, including plastics, coatings, and adhesives.
Used as a Reagent in Organic Synthesis:
2,4-Dihydroxybenzil serves as a reagent in organic synthesis, facilitating various chemical reactions. Its presence can enhance the efficiency and selectivity of these reactions, making it an essential component in many organic synthesis processes.
Used in Medicine:
2,4-Dihydroxybenzil's antioxidant properties make it a potential candidate for use in medicine. Its ability to neutralize harmful free radicals can contribute to the development of treatments for various diseases and conditions.
Used in Skin Care:
The antioxidant properties of 2,4-dihydroxybenzil also make it a promising ingredient in skin care products. Its potential to protect the skin from oxidative stress and promote overall skin health can be beneficial in the development of skincare formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 87538-42-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,3 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87538-42:
(7*8)+(6*7)+(5*5)+(4*3)+(3*8)+(2*4)+(1*2)=169
169 % 10 = 9
So 87538-42-9 is a valid CAS Registry Number.
87538-42-9Relevant articles and documents
Iron-catalyzed ortho-selective functionalization of phenols: A straightforward strategy towards the 2′-hydroxyphenyl-1,2-dione skeleton
Guo, Xingwei,Li, Wenjuan,Li, Zhiping
experimental part, p. 5787 - 5790 (2011/01/04)
An iron-catalyzed ortho-functionalization of phenols was developed. The reactions of simple phenols with α-hydroxy ketones provide a novel and efficient method to construct 2′-hydroxyphenyl-1,2-dione derivatives. An iron-catalyzed ortho-functionalization of phenols was developed. The reactions of simple phenols with α-hydroxy ketonesprovide a novel and efficient method to construct 2′-hydroxyphenyl-1,2-dione derivatives.
FACILE OXIDATION OF o-HYDROXYPHENYL BENZYL KETONES TO UNSYMMETRICAL BENZILS WITH DIMETHYL SULPHOXIDE/POTASSIUM HYDROXIDE
Saxena, Shabnam,Jain, P. K.,Makrandi, J. K.,Grover, S. K.
, p. 3401 - 3402 (2007/10/02)
o-Hydroxyphenyl benzyl ketones on treatment with dimethyl sulphoxide and powdered potassium hydroxide have been found to undergo facile oxidation to the corresponding benzils.
