500729-87-3 Usage
Uses
Used in Organic Synthesis:
2,4-Dimethyl-3,5-dinitroaniline is used as a reagent in organic synthesis for the preparation of various organic chemicals. Its presence of both nitro and aniline functional groups makes it a versatile building block in the synthesis of a wide range of compounds.
Used in Dye and Pigment Production:
DMA is utilized in the production of dyes and pigments due to its yellow color. Its chemical properties allow it to be incorporated into various formulations, contributing to the coloration of different materials.
Used in Pharmaceutical Industry:
2,4-Dimethyl-3,5-dinitroaniline is used as a precursor in the synthesis of pharmaceuticals. Its unique chemical structure enables the development of new drugs with potential therapeutic applications.
Used as a Pesticide and Herbicide:
In agriculture, DMA is employed as a pesticide and herbicide, particularly for the control of broadleaf weeds in crops such as wheat, maize, and barley. Its effectiveness in controlling unwanted plant growth contributes to improved crop yields and quality.
However, it is important to note that 2,4-dimethyl-3,5-dinitroaniline is considered toxic and potentially harmful to human health and the environment. Therefore, proper safety measures should be taken when handling, storing, and using this chemical to minimize any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 500729-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,7,2 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 500729-87:
(8*5)+(7*0)+(6*0)+(5*7)+(4*2)+(3*9)+(2*8)+(1*7)=133
133 % 10 = 3
So 500729-87-3 is a valid CAS Registry Number.
500729-87-3Relevant academic research and scientific papers
Thermal Stability Studies on a Homologous Series of Nitroarenes
Oxley, Jimmie C.,Smith, James L.,Ye, Hong,McKenney, Robert L.,Bolduc, Paul R.
, p. 9593 - 9602 (2007/10/02)
The thermal stabilities of a number of nitroarenes were examined in solution and in condensed phase.In general, increasing the number of nitro groups decreased thermal stability.Changing the substituent on 1-X-2,4,6-trinitrobenzene from X = H to NH2 to CH3 to OH accelerated decomposition; this effect was attributed to increased ease of intramolecular proton transfer to an ortho nitro group, thus weakening the carbon-nitrogen bond.In solution, the effect of increasing substitution from n = 1 to n = 3 on Xn(NO2)3C6H3-n was uniformly that of decreasing the thermal stability of the species.However, in condensed phase, results suggested that crystal habit may be more important than molecular structure; for X = Br, CH3, and NH2, the more substituted species was the more stable.
