3830-64-6 Usage
Uses
Used in Pharmaceutical Industry:
3-Chloro-N-[2-(trifluoroMethyl)phenyl]benzaMide, 97% is used as an intermediate or active pharmaceutical ingredient for the development of new drugs, particularly in the treatment of various diseases and conditions. Its unique chemical structure may offer specific therapeutic properties, making it a valuable compound in drug discovery and design.
Used in Agrochemical Industry:
3-Chloro-N-[2-(trifluoroMethyl)phenyl]benzaMide, 97% is used as a precursor or active ingredient in the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties may contribute to the development of effective and targeted agrochemicals for crop protection and management.
Used in Materials Science:
3-Chloro-N-[2-(trifluoroMethyl)phenyl]benzaMide, 97% is used as a building block or functional component in the development of advanced materials with specific properties. Its unique structure and reactivity may enable the creation of new materials with applications in various industries, such as electronics, coatings, and polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 3830-64-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,3 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3830-64:
(6*3)+(5*8)+(4*3)+(3*0)+(2*6)+(1*4)=86
86 % 10 = 6
So 3830-64-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H9ClF3NO/c15-10-5-3-4-9(8-10)13(20)19-12-7-2-1-6-11(12)14(16,17)18/h1-8H,(H,19,20)
3830-64-6Relevant academic research and scientific papers
Visible-Light Mediated ortho-Trifluoromethylation of Aniline Derivatives
Tian, Chao,Wang, Qiyue,Wang, Xueqi,An, Guanghui,Li, Guangming
, p. 14241 - 14247 (2019/10/16)
A general visible-light mediated ortho-C-H trifluoromethylation of aniline derivatives by using a low-cost and stable Langlois reagent (CF3SO2Na) as the "CF3" source has been developed. In contrast to previous reports, this strategy allowed access to elusive trifluoromethyl lactams. Furthermore, mechanism experiments revealed that a copper/photoredox dual catalytic mechanism enabled general trifluoromethylation of aniline derivatives.
