25743-56-0 Usage
Description
4-Acetoxypropiophenone, also known as p-acetoxypropiophenone, is a chemical compound with the formula C11H12O3. It is a white solid that is commonly used as an intermediate in the synthesis of pharmaceuticals, dyes, and fragrances. This propiophenone is substituted with an acetyloxy group at position 4, and is known for its reactivity and ability to undergo nucleophilic addition reactions.
Uses
Used in Pharmaceutical Industry:
4-Acetoxypropiophenone is used as an intermediate in the synthesis of various pharmaceuticals for its reactivity and ability to undergo nucleophilic addition reactions, contributing to the development of new drugs and medicines.
Used in Dye Industry:
In the dye industry, 4-acetoxypropiophenone is used as an intermediate for the production of different types of dyes, leveraging its chemical properties to create a range of colorants for various applications.
Used in Fragrance Industry:
4-Acetoxypropiophenone is used as an intermediate in the synthesis of fragrances, where its chemical structure plays a role in creating various scent profiles for use in perfumes, cosmetics, and other scented products.
Used as a Precursor in Chemical Industry:
4-Acetoxypropiophenone serves as a precursor for the production of other important chemicals, highlighting its versatility and potential applications across the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 25743-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,4 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25743-56:
(7*2)+(6*5)+(5*7)+(4*4)+(3*3)+(2*5)+(1*6)=120
120 % 10 = 0
So 25743-56-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O3/c1-3-11(13)9-4-6-10(7-5-9)14-8(2)12/h4-7H,3H2,1-2H3
25743-56-0Relevant articles and documents
Visible-Spectrum Solar-Light-Mediated Benzylic C-H Oxygenation Using 9,10-Dibromoanthracene As an Initiator
Santra, Sourav K.,Szpilman, Alex M.
, p. 1164 - 1171 (2020/12/23)
We report a visible-light-mediated benzylic C-H oxygenation reaction. The reaction is initiated by solar light or the blue LED activation of 9,10-dibromoanthracene in a reaction with oxygen and takes place at ambient temperature and air pressure. Secondary benzylic positions are oxygenated to ketones, while tertiary benzylic carbons are oxygenated to give hydroperoxides. Notably, cumene hydroperoxide is produced in a higher yield and at milder conditions than the currently employed industrial conditions.