28315-73-3 Usage
Uses
Used in Pharmaceutical Synthesis:
(4-chlorophenyl)(4-phenoxyphenyl)methanone is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of new drugs with specific therapeutic properties, making it a valuable component in the development of novel medications.
Used in Agrochemical Production:
In the agrochemical industry, (4-chlorophenyl)(4-phenoxyphenyl)methanone serves as a key building block for the production of various agrochemicals. Its incorporation into these compounds can enhance their effectiveness in protecting crops and controlling pests.
Used in Materials Science:
(4-chlorophenyl)(4-phenoxyphenyl)methanone is also utilized in materials science, where it can be used to develop new materials with specific properties. Its unique chemical structure allows for the creation of materials with tailored characteristics, such as improved strength, durability, or chemical resistance.
Used as a Reagent in Chemical Reactions:
Due to its reactive nature, (4-chlorophenyl)(4-phenoxyphenyl)methanone is employed as a reagent in various chemical reactions. It can be used to facilitate specific transformations or to produce desired products with high selectivity and efficiency.
Check Digit Verification of cas no
The CAS Registry Mumber 28315-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,1 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28315-73:
(7*2)+(6*8)+(5*3)+(4*1)+(3*5)+(2*7)+(1*3)=113
113 % 10 = 3
So 28315-73-3 is a valid CAS Registry Number.
28315-73-3Relevant academic research and scientific papers
One pot synthesis of unsymmetrical ketones from carboxylic and boronic acids via PyClU-mediated acylative Suzuki coupling
Garcia-Barrantes, Pedro M.,McGowan, Kevin,Ingram, Steven W.,Lindsley, Craig W.
, p. 898 - 901 (2017/02/10)
A synthetic procedure for the preparation of ketones from easily accessible carboxylic acids has been developed. This methodology proceeds via in situ activation of the carboxylic acid with PyClU, followed by the palladium-catalyzed acylative cross-coupling with boronic acids. The reaction is performed in one pot, without the need of phosphine ligands, at room temperature and in reaction times of 2 h or less. The scope of the reaction is robust with aryl boronic and carboxylic acids.
