25843-74-7 Usage
General Description
2-[(4-methoxyphenyl)amino]benzohydrazide is a chemical compound that belongs to the class of hydrazides. It is also known as N?-(4-methoxyphenyl)benzohydrazide. 2-[(4-methoxyphenyl)amino]benzohydrazide is commonly used in the field of medicinal chemistry due to its potential pharmaceutical properties. It has been studied for its antimicrobial, anti-inflammatory, and anticancer activities. Additionally, it has shown potential as an inhibitor of enzymes involved in the production of reactive oxygen species, making it a promising candidate for the development of new therapeutic agents. The compound's structure and properties make it a subject of interest for further research and potential applications in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 25843-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,4 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25843-74:
(7*2)+(6*5)+(5*8)+(4*4)+(3*3)+(2*7)+(1*4)=127
127 % 10 = 7
So 25843-74-7 is a valid CAS Registry Number.
25843-74-7Relevant academic research and scientific papers
COMPOSES SULFURES HETEROCYCLIQUES. XCVI. REACTION DE L'HYDRAZINE SUR LES DIHYDRO-1,2 BENZOTHIAZINE-3,1 THIONES-4
Legrand, Louis,Lozac'H, Noel
, p. 139 - 143 (2007/10/02)
1-Alkyl-1,2-dihydro-3,1-benzothiazine-4-thiones 1, when reacting with hydrazine, give with a good yield a 1-alkyl-3-amino-2,3-dihydro-1H-quinazoline-4-thione-2, often together with a derivative of 1,3,4-thiadiazole-3. With 1-aryl-1,2-dihydro-3,1-benzothiazine-4-thiones, the main product of the reaction with hydrazine appears to be a 1-aryl-4-hydrazono-1,4-dihydro-2H-3,1-benzothiazine 4, sometimes with some amount of 3.On the contrary, when reacting with hydrazine, 1-alkyl (or 1-aryl)-1,2-dihydro-3,1-benzothiazin-4-ones lead to a 2-alkylamino (or arylamino)-benzohydrazide 5. By thermolysis 4 isomerizes into 2 which is accompanied by derivatives (3 and 7) of 1,3,4-thiadiazole.The structures of compounds 2, 4 and 7 have been studied by NMR and UV spectrometry.
