2217-45-0 Usage
Uses
Used in Chemical Synthesis Industry:
2,3,4,5-tetramethylaniline is used as an intermediate for the production of dyes, pharmaceuticals, and other organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of various specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2,3,4,5-tetramethylaniline serves as a key intermediate in the synthesis of certain drugs. Its presence in the molecular structure of these compounds contributes to their therapeutic properties, highlighting its importance in medicinal chemistry.
Used in Dye Industry:
2,3,4,5-tetramethylaniline is utilized as a precursor in the manufacturing process of dyes. Its chemical properties enable the creation of a wide range of colorants used in various applications, such as textiles, plastics, and printing inks.
Safety and Handling:
Due to its potential to cause skin and eye irritation, as well as respiratory and other serious health effects, 2,3,4,5-tetramethylaniline should be handled and stored with caution. Proper safety measures, including the use of personal protective equipment and adherence to safety protocols, are essential to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 2217-45-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2217-45:
(6*2)+(5*2)+(4*1)+(3*7)+(2*4)+(1*5)=60
60 % 10 = 0
So 2217-45-0 is a valid CAS Registry Number.
2217-45-0Relevant academic research and scientific papers
REDUCTION OF AROMATIC NITRO COMPOUNDS WITH SODIUM TELLURIDE
Suzuki, Hitomi,Manabe, Hajime,Inouye, Masahiko
, p. 1671 - 1674 (2007/10/02)
Sodium telluride, prepared by heating tellurium with Rongalite in aqueous sodium hydroxide, easily reduces aromatic nitro compounds to the corresponding amines in good yields.The reduction can be carried out using a catalytic amount of tellurium, since sodium telluride is readily regenerated in the presence of excess Rongalite.
Onium Ions. 26. Aminodiazonium Ions: Preparation, 1H, 13C, and 15N NMR Structural Studies, and Electrophilic Amination of Aromatics
Mertens, Alfred,Lammerstma, Koop,Arvanaghi, Massoud,Olah, George A.
, p. 5657 - 5660 (2007/10/02)
Protonation of hydrazoic acid and alkyl azides with FSO3/SbF5, HF/SbF5, or HF/BF3 results in the formation of stable aminodiazonium ions as shown by 1H, 13C, and 15N NMR spectroscopic studies.Molecular orbital calculations of the thermodynamics of the protonation of hydrazoic acid also support preferential formation of the aminodiazonium ion.The aminodiazonium ion was also prepared in situ from NaN3/AlCl3/HCl or (CH3)3SiN3/AlCl3/HCl .Aminodiazonium salts were found to affect electrophilic amination of aromatics in high yields, with generally high regioselectivity and low substrate selectivity.
