622-74-2 Usage
Description
(1E)-1-(4-methylphenyl)-3-phenyltriaz-1-ene, also known as 1-phenyl-3-(4-tolyl)-1H-triazene, is a triazene compound characterized by a triazene ring attached to a phenyl group and a methylphenyl group. It has been studied for its potential as an anticancer agent and its ability to undergo photochemical reactions. The specific properties and applications of this compound would depend on its individual characteristics and potential reactivity, which may require further research and testing to fully understand.
Uses
Used in Pharmaceutical Industry:
(1E)-1-(4-methylphenyl)-3-phenyltriaz-1-ene is used as a potential anticancer agent for its ability to target and inhibit the growth of cancer cells. Its triazene structure and reactivity may contribute to its potential effectiveness in treating various types of cancer.
Used in Chemical Research:
(1E)-1-(4-methylphenyl)-3-phenyltriaz-1-ene is used as a subject of study in chemical research for its photochemical properties and reactivity. Understanding its behavior in different conditions can provide insights into the development of new compounds and applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 622-74-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 622-74:
(5*6)+(4*2)+(3*2)+(2*7)+(1*4)=62
62 % 10 = 2
So 622-74-2 is a valid CAS Registry Number.
622-74-2Relevant articles and documents
Metal-Free One-Pot Synthesis of N,N′-Diarylamidines and N-Arylbenzimidazoles from Arenediazonium Salts, Nitriles, and Free Anilines
Youn, So Won,Lee, Eun Mi
supporting information, p. 5728 - 5731 (2016/11/17)
A highly efficient and facile metal-free, one-pot reaction has been developed to afford diversely substituted N-arylbenzimidazoles through chemoselective in situ generation of N,N′-diarylamidines from arenediazonium salts, nitriles, and free anilines. The advantages of this protocol consist of the operationally easy and simple one-pot procedure under metal-free and mild conditions, the direct use of inexpensive and commercially available chemicals, and thus, a cost-effective and greener process.
Pd-catalyzed C-H activation/C-N bond formation: A new route to 1-aryl-1H-benzotriazoles
Kumar, Rapolu Kiran,Ali, Md Ashif,Punniyamurthy, Tharmalingam
supporting information; experimental part, p. 2102 - 2105 (2011/06/25)
A method for the C-H activation of aryl triazene compounds followed by intramolecular amination is described. It involves the use of a catalytic amount of Pd(OAc)2 that efficiently effects the cyclization to provide 1-aryl-1H-benzotriazoles at moderate temperature.
