60418-61-3 Usage
Phenylamine class
The compound belongs to the phenylamine class of chemicals, which are derivatives of aniline and have a wide range of applications in pharmaceuticals, agrochemicals, and materials science.
Pyrazole ring
The presence of a pyrazole ring in the structure of the compound, which is a five-membered heterocyclic ring containing two nitrogen atoms and one oxygen atom. This ring contributes to the compound's unique properties and potential applications.
Trifluoromethyl group
The presence of a trifluoromethyl (CF3) group, which is an electron-withdrawing group that can influence the compound's reactivity, stability, and solubility in various solvents.
Dimethyl groups
The presence of two dimethyl (CH3) groups, which are electron-donating groups that can affect the compound's reactivity and stability.
Unique properties
The combination of trifluoromethyl and dimethyl groups in the compound's structure gives it unique properties, such as increased lipophilicity and potential for hydrogen bonding, which can be useful in various applications.
Potential applications
2-(3,5-Dimethyl-pyrazol-1-yl)-5-trifluoromethyl-phenylamine may be used in pharmaceutical research, organic synthesis, or other chemical processes due to its unique properties and structure.
Context-dependent uses
The specific uses and properties of the compound may vary depending on the context and intended application, such as its use as an intermediate in the synthesis of other compounds or as a pharmaceutical agent with specific therapeutic effects.
Check Digit Verification of cas no
The CAS Registry Mumber 60418-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,1 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60418-61:
(7*6)+(6*0)+(5*4)+(4*1)+(3*8)+(2*6)+(1*1)=103
103 % 10 = 3
So 60418-61-3 is a valid CAS Registry Number.
60418-61-3Relevant academic research and scientific papers
Competitive Cyclisations of Singlet and Triplet Nitrenes. Part 8. The 1-(2-Nitrenophenyl)pyrazoles and Related Systems
Lindley, John M.,McRobbie, Ian M.,Meth-Cohn, Otto,Suschitzky, Hans
, p. 982 - 994 (2007/10/02)
The title nitrenes, derived by nitro-group deoxygenation with triethyl phosphite or by thermolysis or photolysis of the corresponding azide, have been studied.The effect of substituents (Cl, Br, OMe, NMe2, Me, CF3, and NO2) both meta and para to the nitrene has been examined as a determinant of the preferred mode of cyclisation to either a pyrazolobenzotriazole or a pyrazoloquinoxaline.Similarly, the role of solvents, sensitisers, and quenchers has been studied.Routes to the isomeric 1- and 2-(2-nitrophenyl)-4,5,6,7-tetrahydroindazoles have been defined and the literature corrected by studing the nitrene-mediated cyclisation of these products.The chemistry of the analogous 1-(2-carbenophenyl)- and the 1-(2-nitrenosulphonylphenyl)-3,5-dimethylpyrazoles has also been examined, the former giving 2-(3,5-dimethylpyrazol-1-yl)-benzaldazine and -benzyl alcohol while the latter gave products of intramolecular nitrene attack (a pyrazolobenzothiatriazine) and intermolecular reaction.Rationalisations for all the reaction pathways have been advanced.
