40306-24-9 Usage
Uses
Used in Pharmaceutical Industry:
4-Chloro-4'-methyl-3-nitrobenzophenone is used as an intermediate compound for the synthesis of nitrogen-containing heterocycles. These heterocycles are vital in the development of various pharmaceutical products due to their diverse biological activities and potential therapeutic applications.
Used in Chemical Industry:
In the chemical industry, 4-chloro-4'-methyl-3-nitrobenzophenone serves as a key building block for the creation of complex organic molecules. Its unique structure allows for further functionalization and modification, making it a valuable component in the synthesis of specialty chemicals and advanced materials.
Overall, 4-chloro-4'-methyl-3-nitrobenzophenone plays a crucial role in both the pharmaceutical and chemical industries, contributing to the development of novel compounds with potential applications in medicine, materials science, and other related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 40306-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,0 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 40306-24:
(7*4)+(6*0)+(5*3)+(4*0)+(3*6)+(2*2)+(1*4)=69
69 % 10 = 9
So 40306-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H10ClNO3/c1-9-2-4-10(5-3-9)14(17)11-6-7-12(15)13(8-11)16(18)19/h2-8H,1H3
40306-24-9Relevant academic research and scientific papers
An improved procedure for the regiospecific synthesis of electron deficient 4- and 6-substituted isatins
Kraynack, Erica A.,Dalgard, Jackline E.,Gaeta, Federico C. A.
, p. 7679 - 7682 (2007/10/03)
The regiospecific synthesis of 4- and 6-substituted isatins 5a-g in four steps from halonitrobenzenes 1a-g has been investigated for a variety of substrates (Scheme 1). The procedure makes use of readily available, easily handled materials and in most cases purification of neither intermediates nor final products is required. Yields of isatins are between 26 and 75% (Table 1). Improved yields of known isatins are reported as well as the syntheses of previously unreported isatins. This method, taken together with known procedures, provides for the synthesis of the full complement of isatin regioisomers.
