75616-92-1 Usage
Uses
Used in Pharmaceutical Applications:
(Phenanthro[9,10-e][1,2,4]triazin-3-ylsulfanyl)acetic acid is used as an anti-inflammatory agent for its potential to alleviate inflammation, which can be beneficial in treating various conditions characterized by inflammation.
(Phenanthro[9,10-e][1,2,4]triazin-3-ylsulfanyl)acetic acid is used as an antioxidant agent for its potential to neutralize harmful free radicals, which can contribute to the prevention or treatment of oxidative stress-related diseases.
Used in Cancer Therapy:
(Phenanthro[9,10-e][1,2,4]triazin-3-ylsulfanyl)acetic acid is used as a cytotoxic agent for its demonstrated effects on certain cancer cell lines, potentially making it a valuable compound in the development of novel cancer treatments.
Used in Research and Development:
(Phenanthro[9,10-e][1,2,4]triazin-3-ylsulfanyl)acetic acid is used as a compound of interest in the field of medical research for its potential therapeutic applications in various medical fields, including the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 75616-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,1 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75616-92:
(7*7)+(6*5)+(5*6)+(4*1)+(3*6)+(2*9)+(1*2)=151
151 % 10 = 1
So 75616-92-1 is a valid CAS Registry Number.
75616-92-1Relevant academic research and scientific papers
Condensed 1,2,4-Triazines, III
Ram, Vishnu Ji,Pandey, Hrishi Kesh
, p. 465 - 471 (2007/10/02)
Alkylation of 3-mercaptophenanthreno-1,2,4-triazine (1b) yielded the S-alkyl derivatives 2a-d.Amination of 1a afforded the 3-amino derivatives 3a-h.Reaction of 1a with hydrazine hydrate gave 3-hydrazinophenanthreno-1,2,4-triazine (4) which underwent cyclisation with nitrous, formic or acetic acids giving the phenanthreno-1,2,4-triazino-1,2,3,4-tetrazole (5) and the phenanthreno-1,2,4-triazino-3H-methyl-1,2,4-triazoles 6, 7.Compound 4 also reacted with methyl cyanoacetate, ethyl acetoacetate, ethoxymethylenemalononitrile, ethyl ethoxymethylencyanoacetate or acetyl acetone to yield the 3-(pyrazol-1-yl)-phenanthreno-1,2,4-triazines 8-12.
