4406-68-2 Usage
Uses
Used in Chemical Synthesis:
(Methyl-NNO-azoxy)benzene is used as an intermediate in the chemical synthesis industry for the production of dyes and pigments. Its unique chemical structure allows for the creation of a wide range of colored compounds, making it a valuable component in this application.
Used in Rubber and Plastics Manufacturing:
In the rubber and plastics industry, (Methyl-NNO-azoxy)benzene is employed as a crucial component in the manufacturing process. Its inclusion in the production of these materials contributes to their overall properties, such as durability and flexibility.
Used in Hazardous Chemical Handling and Storage:
Given its classification as a hazardous chemical, (Methyl-NNO-azoxy)benzene necessitates specific handling and storage protocols to ensure the safety of workers and minimize environmental impact. This application involves the development and implementation of safety measures, such as proper containment, ventilation, and disposal methods, to mitigate potential risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 4406-68-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,0 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4406-68:
(6*4)+(5*4)+(4*0)+(3*6)+(2*6)+(1*8)=82
82 % 10 = 2
So 4406-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O/c1-8-9(10)7-5-3-2-4-6-7/h2-6H,1H3/b9-8-
4406-68-2Relevant academic research and scientific papers
Difference in the reactions of N-methylhydroxylamine and N-phenylhydroxylamine with nitrosobenzene
Dal Magro, Jacir,Yunes, Rosendo Augusto
, p. 2381 - 2385 (2007/10/03)
The reaction of nitrosobenzene with N-methylhydroxylamine was studied. The pH-rate profile exhibits a negative break at between pH 0.5 and 3.0, which is considered to be caused by a change in the rate-determining step of the reaction from an attack of the amine on nitrosobenzene at low pH, to the dehydration of an addition intermediate previously formed between the reagents at higher pH. This behavior is different from that of the reaction between N-phenylhydroxylamine and nitrosobenzene where, over the entire pH range, the only rate-determining step is dehydration of the addition intermediate. This fact confirms the special behavior of phenylhydroxylamine as a nucleophile, as was observed in its reactions with aromatic aldehydes.
Investigations on the stability of l-methyl-2-phenylacetohydrazide
Bresser,Weber
, p. 470 - 476 (2007/10/03)
l-Methyl-2-phenylacetohydrazide (1), a degradation product of dipyrone, is hydrolytically stable. In contrast it is oxidized into several products like 3a/3b, 4 and 5a/5b. The composition of the reaction mixture depends on the oxidation conditions (ferricyanide; hydrogenperoxide with/without peroxidase; pH 5-9) and was determined by capillary column gaschromatography.
