41512-62-3 Usage
Uses
Used in Agrochemicals and Pharmaceuticals:
3-Trifluoromethyl-N,N-dimethyl-4-nitroaniline is utilized as a key intermediate in the manufacturing process of agrochemicals and pharmaceuticals. Its unique structure allows for the development of compounds with specific biological activities, contributing to its importance in these industries.
Used as a Dye Intermediate:
In the dye industry, 3-Trifluoromethyl-N,N-dimethyl-4-nitroaniline serves as an intermediate for the production of various dyes. Its chemical properties facilitate the creation of dyes with distinct color characteristics and stability.
Used in the Preparation of Other Organic Compounds:
3-Trifluoromethyl-N,N-dimethyl-4-nitroaniline is also employed in the synthesis of a range of other organic compounds, showcasing its adaptability in organic chemistry and its potential for use in multiple applications across different fields.
Used as an Intermediate for Biologically Active Compounds:
Recognizing its potential, 3-Trifluoromethyl-N,N-dimethyl-4-nitroaniline is used as an intermediate in the synthesis of biologically active compounds. Its incorporation into these compounds can lead to the development of new pharmaceuticals and other bioactive substances with potential therapeutic or commercial value.
Check Digit Verification of cas no
The CAS Registry Mumber 41512-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,5,1 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41512-62:
(7*4)+(6*1)+(5*5)+(4*1)+(3*2)+(2*6)+(1*2)=83
83 % 10 = 3
So 41512-62-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9F3N2O2/c1-13(2)6-3-4-8(14(15)16)7(5-6)9(10,11)12/h3-5H,1-2H3
41512-62-3Relevant academic research and scientific papers
Photoassisted Charge Transfer Between DMF and Substrate: Facile and Selective N,N-Dimethylamination of Fluoroarenes
Ansari, Tharique N.,Sharma, Sudripet,Bora, Pranjal P.,Ogulu, Deborah,Parmar, Saurav,Gallou, Fabrice,Kozlowski, Pawel M.,Handa, Sachin
, p. 2704 - 2709 (2021/06/09)
A reversible Van der Waals complex formation between the electron-deficient fluorinated aromatic ring and N,N-dimethylformamide (DMF) molecules followed by light irradiation resulted in charge transfer (CT) process. The complex was stabilized by ammonium formate and further decomposed to form the C?N bond. Control experiments revealed that the simultaneous SNAr pathway also contributes to product formation. This methodology is mild, metal-free, and effective for the amination of a variety of substrates. The reproducibility of this methodology was also verified on gram-scale reactions. The CT states were supported by control UV/Vis spectroscopy and computational studies.
Unusual aminations with tetramethylguanidine
Gabbutt, Christopher D.,Heron, B. Mark,McCreary, Janice M.,Thomas, David A.
, p. 69 - 71 (2007/10/03)
Heating activated halobenzenes with 1,1,3,3-tetramethylguanidine affords mixtures of dimethylaminobenzenes and 2-aryl-1,1,3,3-tetramethylguanidines.
