203710-89-8 Usage
Uses
Used in Pharmaceutical Industry:
N-(4-bromophenyl)-3-methyl-N-(m-tolyl)aniline is utilized as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Dye Industry:
N-(4-broMophenyl)-3-Methyl-N-(M-tolyl)aniline serves as an intermediate in the production of dyes, playing a crucial role in the creation of colorants for various applications, including textiles, plastics, and printing inks.
Used in Agrochemical Industry:
N-(4-bromophenyl)-3-methyl-N-(m-tolyl)aniline is employed in the synthesis of agrochemicals, aiding in the development of pesticides and other agricultural chemicals to enhance crop protection and productivity.
Used in Organic Chemistry Research:
Due to its unique structure and reactivity, N-(4-broMophenyl)-3-Methyl-N-(M-tolyl)aniline is valuable in organic chemistry research, facilitating the exploration of new chemical reactions and the synthesis of novel organic compounds.
Used in Specialty Chemicals Production:
N-(4-bromophenyl)-3-methyl-N-(m-tolyl)aniline is also used in the production of certain specialty chemicals, where its specific properties are leveraged to create high-value products for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 203710-89-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,7,1 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 203710-89:
(8*2)+(7*0)+(6*3)+(5*7)+(4*1)+(3*0)+(2*8)+(1*9)=98
98 % 10 = 8
So 203710-89-8 is a valid CAS Registry Number.
203710-89-8Relevant academic research and scientific papers
Kanazawa, Yoshinori,Yokota, Tomo,Ogasa, Hiroshi,Watanabe, Hirotaka,Hanakawa, Taisyun,Soga, Shinichi,Kawatsura, Motoi
, p. 1395 - 1402 (2015)
We report the chemoselective amination of bromoiodobenzenes with diarylamines by palladium/Xantphos or a ligand-free copper catalyst. The reactions by these two types of catalysts proceeded with a high chemoselectivity and afforded monobrominated triarylamines in good yields. These products are useful intermediates for the synthesis of unsymmetrical bistriarylamines.
