63333-31-3 Usage
Description
2,4-dinitro-N-phenyl-6-(trifluoromethyl)aniline is an organic compound that serves as an intermediate in the synthesis of various chemical compounds. It is characterized by the presence of nitro and trifluoromethyl groups, which contribute to its chemical properties and potential applications.
Uses
Used in Pesticide Synthesis:
2,4-dinitro-N-phenyl-6-(trifluoromethyl)aniline is used as an intermediate in the synthesis of Bromethalin (B633330), a pesticide that protects plants from insect pests. It acts as an attractant, chemosterilant, and rodenticide for effective mice pest control, ensuring the health and productivity of crops.
Used in Chemical Research:
In addition to its role in pesticide synthesis, 2,4-dinitro-N-phenyl-6-(trifluoromethyl)aniline can be utilized in chemical research for the development of new compounds with potential applications in various industries. Its unique structure and functional groups make it a valuable building block for the creation of novel molecules with specific properties and functions.
Check Digit Verification of cas no
The CAS Registry Mumber 63333-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,3 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63333-31:
(7*6)+(6*3)+(5*3)+(4*3)+(3*3)+(2*3)+(1*1)=103
103 % 10 = 3
So 63333-31-3 is a valid CAS Registry Number.
63333-31-3Relevant articles and documents
Kinetics of the reaction of 2-chloro-3,5-dinitrobenzotriflouride with aniline in toluene and methanol-toluene mixed solvents
Fathalla, Magda F.
, p. 109 - 114 (2012)
Kinetics of the reaction of 2-chloro-3,5-dinitrobenzotriflouride with aniline were studied in toluene, methanol-toluene binary solvents, benzene and chloroform. The reaction in toluene exhibits third-order kinetics consistent with aggregates of aniline. Thermodynamic parameters ΔH#, ΔS# and ΔG#are calculated and discussed for the reaction of 2-chloro-3,5-dinitrobenzotriflouride with aniline in methanol-toluene. Molecular complexes between aniline and the substrate are rejected spectrophotometricaly. The mechanism is studied and compared with the reaction in presence of pyridine. It shows an amine dependence and formation of homo and/or hetero mixed aggregates between aniline and pyridine i.e. dimer mechanism. Copyright
