63113-39-3 Usage
Uses
Used in Pharmaceutical Synthesis:
[1,1'-Biphenyl]-3-amine, N,N,6-trimethylis used as a key intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure and reactivity allow for the creation of a wide range of therapeutic compounds, contributing to the development of novel medications.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, [1,1'-Biphenyl]-3-amine, N,N,6-trimethylserves as a vital building block for the synthesis of complex organic compounds. Its presence in these compounds can significantly influence their properties and potential applications, making it an essential component in organic synthesis.
Used in Research and Development:
[1,1'-Biphenyl]-3-amine, N,N,6-trimethylis also extensively utilized in research and development, where it aids in the exploration of new chemical reactions, mechanisms, and the development of innovative synthetic routes. Its unique properties and reactivity make it a valuable tool for scientists and researchers in the field of organic chemistry.
Used in Specialty Chemicals Production:
[1,1'-Biphenyl]-3-amine, N,N,6-trimethylis employed in the production of specialty chemicals, where its unique structure and properties contribute to the development of high-value products with specific applications in various industries, such as materials science, electronics, and coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 63113-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,1 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63113-39:
(7*6)+(6*3)+(5*1)+(4*1)+(3*3)+(2*3)+(1*9)=93
93 % 10 = 3
So 63113-39-3 is a valid CAS Registry Number.
63113-39-3Relevant academic research and scientific papers
Acid-Catalyzed Reactions of N-Arylhydroxylamines and Related Compounds with Benzene. Iminium-Benzenium Ions
Shudo, Koichi,Ohta, Toshiharu,Okamoto, Toshihiko
, p. 645 - 653 (2007/10/02)
N-Arylhydroxylamines react with benzene in the presence of trifluoroacetic acid (TFA) at room temperature to give diphenylamines.When TFA was replaced by a strong acid, trifluoromethanesulfonic acid (TFSA), the major products were aminobiphenyls.The nature of the reaction was explored by reactions of 4-substituted phenylhydroxylamines and dialkylaniline N-oxides with benzene.Thus, it was demonstrated that the reactive intermediates are onium-benzenium dications which are trapped by benzene to give aminobiphenyls by a mechanism similar to the Friedel-Krafts alkylation.Further evidence for the proposed reaction mechanism was the observation that nitrosobenzene and azoxybenzene reacted with benzene to give analogous products in the presence of the stronger acid.
