125065-88-5 Usage
Uses
Used in Pharmaceutical Industry:
2,5-Cyclohexadien-1-one, 4-methyl-2,4-dinitrois used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure and reactivity enable the production of a wide range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Organic Chemistry:
In the field of organic chemistry, 2,5-Cyclohexadien-1-one, 4-methyl-2,4-dinitrois utilized as a building block for the synthesis of complex organic molecules. Its versatile reactivity allows for the formation of various functional groups and the construction of intricate molecular architectures.
Used in High-Energy Materials:
2,5-Cyclohexadien-1-one, 4-methyl-2,4-dinitrois employed as a key component in the development of high-energy materials. Its explosive and oxidizing properties make it suitable for applications in propellants, explosives, and other energetic systems, where high energy release is required.
Used in Explosive Manufacturing:
Due to its high reactivity and energy content, 2,5-Cyclohexadien-1-one, 4-methyl-2,4-dinitrois used in the manufacture of various types of explosives. Its incorporation into explosive formulations enhances their performance, making it a valuable component in the production of military and industrial explosives.
Check Digit Verification of cas no
The CAS Registry Mumber 125065-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,0,6 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 125065-88:
(8*1)+(7*2)+(6*5)+(5*0)+(4*6)+(3*5)+(2*8)+(1*8)=115
115 % 10 = 5
So 125065-88-5 is a valid CAS Registry Number.
125065-88-5Relevant academic research and scientific papers
The Nitration of 4-Methylphenol, 3,4-Dimethylphenol and 3,4,5-Trimethylphenol with Nitrogen Dioxide
Hartshorn, Michael P.,Judd, Maurice C.,Vannoort, Richard W.,Wright, Graeme J.
, p. 689 - 697 (2007/10/02)
Reaction of 4-methylphenol (1a) with excess nitrogen dioxide in either benzene or dichloromethane gives the 4-nitro dienone (2a) and the 2,6-dinitrophenol (5).Similar reactions of 3,4-dimethylphenol (1b) yields the 4-nitro dienone (2b), the 2,6-dinitrophe
