964-75-0 Usage
Uses
Used in Dye Production:
2,4-DINITRO-2'-METHYLDIPHENYLAMINE is used as an intermediate in the production of various dyes. Its chemical structure allows for the synthesis of a range of colorants used in different industries.
Used in Pharmaceutical Synthesis:
2,4-DINITRO-2'-METHYLDIPHENYLAMINE is also utilized in the synthesis of pharmaceuticals, serving as a key building block for the development of new drugs. Its presence in the synthesis process is crucial for creating the desired medicinal properties.
Used in Organic Compound Synthesis:
2,4-DINITRO-2'-METHYLDIPHENYLAMINE is employed as an intermediate in the synthesis of other organic compounds, contributing to the creation of a variety of chemical products across different sectors.
Safety Precautions:
Due to its potential explosive nature and toxicity, it is essential to handle 2,4-DINITRO-2'-METHYLDIPHENYLAMINE with care. It is harmful if swallowed, inhaled, or comes into contact with the skin, and may cause irritation to the respiratory system and skin. Therefore, proper safety measures, including personal protective equipment and controlled environments, must be followed to minimize risks during its use and handling.
Check Digit Verification of cas no
The CAS Registry Mumber 964-75-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 964-75:
(5*9)+(4*6)+(3*4)+(2*7)+(1*5)=100
100 % 10 = 0
So 964-75-0 is a valid CAS Registry Number.
964-75-0Relevant academic research and scientific papers
Oxidative arylamination of 1,3-dinitrobenzene and 3-nitropyridine under anaerobic conditions: The dual role of the nitroarenes
Gulevskaya, Anna V.,Tyaglivaya, Inna N.,Verbeeck, Stefan,Maes, Bert U.W.,Tkachuk, Anna V.
experimental part, p. 238 - 251 (2011/08/22)
1,3-Dinitrobenzene and 3-nitropyridine react with lithium arylamides under anaerobic conditions to produce N-aryl-2,4-dinitroanilines and N-aryl-5-nitropyridin-2-amines, respectively, in 8-42% yields. ARKAT-USA, Inc.
Use of fluorine kinetic isotope effects in the study of steric effects in nucleophilic aromatic substitution reactions
Persson, Jonas,Matsson, Olle
, p. 9348 - 9350 (2007/10/03)
Leaving group fluorine kinetic isotope effects (F KIEs) have been determined in order to probe the influence of steric effects on the mechanism of the nucleophilic aromatic substitution (S(N)Ar) reaction of 2,4- dinitrofluorobenzene (DNFB) with 2- and 4-m
