14575-21-4 Usage
General Description
The chemical compound (1E)-1-(4-methylphenyl)-3-(4-nitrophenyl)triaz-1-ene, also known by its IUPAC name 1-(4-methylphenyl)-3-(4-nitrophenyl)-1H-1,2,4-triazole, is a triazole derivative with a molecular formula C15H12N4O2. It consists of a triazole ring with a 4-methylphenyl group at one end and a 4-nitrophenyl group at the other. (1E)-1-(4-methylphenyl)-3-(4-nitrophenyl)triaz-1-ene has potential applications in pharmaceutical and agricultural industries due to its diverse biological activities, such as anti-inflammatory, antimicrobial, and antifungal properties. Its unique structure and functional groups make it of interest for research and development in the synthesis of new organic compounds with potential therapeutic and agricultural uses.
Check Digit Verification of cas no
The CAS Registry Mumber 14575-21-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,7 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14575-21:
(7*1)+(6*4)+(5*5)+(4*7)+(3*5)+(2*2)+(1*1)=104
104 % 10 = 4
So 14575-21-4 is a valid CAS Registry Number.
14575-21-4Relevant articles and documents
2-Methoxy-4-nitrobenzenediazonium salt as a practical diazonium-transfer agent for primary arylamines via tautomerism of 1,3-diaryltriazenes: Deaminative iodination and arylation of arylamines without direct diazotization
Saeki, Tomoyuki,Son, Eun-Cheol,Tamao, Kohei
, p. 1654 - 1658 (2007/10/03)
1,3-Diaryltriazenes, prepared from a 2-methoxy-4-nitrobenzenediazonium salt and primary arylamines, exist as "azo-transfer" tautomers in which the 2-methoxy-4-nitrophenyl group is present on the saturated nitrogen atom and forms a hydrogen bond between the 2-methoxy group and the N-H moiety. The synthetic utility of the diazonium salt as a practical diazonium-transfer agent for primary arylamines via tautomerism of the 1,3-diaryltriazenes has been demonstrated by the deaminative iodination and arylation of the arylamines without direct diazotization. The starting 2-methoxy-4-nitrophenylamine can be easily recovered after the reactions.
