6304-61-6 Usage
Uses
Used in Organic Synthesis:
1-(2,6-dimethylphenyl)-1-methylhydrazine is used as a reagent in organic synthesis for [application reason] its ability to participate in various chemical reactions, contributing to the formation of a wide range of compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 1-(2,6-dimethylphenyl)-1-methylhydrazine is used as an intermediate for [application reason] its role in the synthesis of various medicinal compounds, aiding in the development of new drugs.
Used in Agrochemicals:
1-(2,6-dimethylphenyl)-1-methylhydrazine is also utilized as an intermediate in the production of agrochemicals for [application reason] its contribution to the creation of chemicals that can be used in the agricultural sector for pest control and other purposes.
Used in Rocket Fuel:
1-(2,6-dimethylphenyl)-1-methylhydrazine is used as a propellant in rocket fuel for [application reason] its high-energy content, which makes it suitable for powering space vehicles and contributing to space exploration and satellite launches.
Used in High-Energy Explosives:
1-(2,6-dimethylphenyl)-1-methylhydrazine is a component in some high-energy explosive mixtures for [application reason] its explosive properties, which are harnessed in specific applications where high energy release is required.
Check Digit Verification of cas no
The CAS Registry Mumber 6304-61-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6304-61:
(6*6)+(5*3)+(4*0)+(3*4)+(2*6)+(1*1)=76
76 % 10 = 6
So 6304-61-6 is a valid CAS Registry Number.
6304-61-6Relevant academic research and scientific papers
REARRANGEMENTS OF AROMATIC CARBONYL ARYLHYDRAZONES OF BENZENE, NAPHTHALENE, AND AZULENE
Benincori, Tiziana,Pagani, Silvia Bradamante,Fusco, Raffaello,Sannicolo, Franco
, p. 2721 - 2728 (2007/10/02)
Aromatic carbonyl arylhydrazones have been shown to undergo two kinds of rearrangement in polyphosphoric acid both involving nitrogen-nitrogen bond cleavage.The first proceeds via insertion of the imine portion in the position ortho to the second nitrogen atom to give o-phenylenediamine intermediates: their evolution depends on the nature of the starting substrate.This reaction has been employed for synthesizing the quinoxalines (5) and the phenanthridines (11), and was demonstrated to be intramolecular.The second reaction path is a sigmatropic rearrangment exclusive to electron-rich aromatic carbonyl hydrazones.
