42191-01-5 Usage
Uses
Used in Organic Synthesis:
5-NITRO-2-(4-CHLOROPHENYLTHIO)BENZALDEHYDE is used as an intermediate in the synthesis of dyes and pigments, contributing to the coloration and stability of these products. Its unique structure allows for versatile chemical reactions, making it a valuable component in the creation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 5-NITRO-2-(4-CHLOROPHENYLTHIO)BENZALDEHYDE serves as a key intermediate for the production of various drugs and medications. Its chemical versatility aids in the development of new therapeutic agents, potentially leading to advancements in medical treatments.
Used in Chemical Research:
5-NITRO-2-(4-CHLOROPHENYLTHIO)BENZALDEHYDE is also utilized in chemical research for studying the properties and reactions of aldehydes, nitro compounds, and thioethers. This helps in understanding the fundamental chemistry involved in the synthesis of related compounds and contributes to the broader field of organic chemistry.
Safety Precautions:
Due to its toxic and potentially harmful nature, 5-NITRO-2-(4-CHLOROPHENYLTHIO)BENZALDEHYDE requires careful handling and the implementation of proper safety measures. This includes the use of personal protective equipment, working in well-ventilated areas, and adhering to established safety protocols to minimize health and environmental risks.
Check Digit Verification of cas no
The CAS Registry Mumber 42191-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,1,9 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 42191-01:
(7*4)+(6*2)+(5*1)+(4*9)+(3*1)+(2*0)+(1*1)=85
85 % 10 = 5
So 42191-01-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H8ClNO3S/c14-10-1-4-12(5-2-10)19-13-6-3-11(15(17)18)7-9(13)8-16/h1-8H
42191-01-5Relevant academic research and scientific papers
Nitroarylhydroxymethylphosphonic acids as inhibitors of CD45
Beers, Scott A.,Malloy, Elizabeth A.,Wu, Wei,Wachter, Michael P.,Gunnia, Uma,Cavender, Druie,Harris, Crafford,Davis, Janet,Brosius, Ruth,Pellegrino-Gensey, J. Lee,Siekierka, John
, p. 2203 - 2211 (2007/10/03)
A series of nitroarylhydroxymethylphosphonic acids was synthesized and evaluated as inhibitors of CD45. It was discovered that both the alpha hydroxy and nitro groups are essential for activity. Potency is enhanced by the addition of a large lipophilic group on the aryl ring adjacent to the phosphonic acid moiety. Kinetics studies have shown that these compounds are competitive inhibitors and thus bind at the active site of this enzyme.
