98317-60-3 Usage
Uses
Used in Pharmaceutical Industry:
(6-methyl-2-oxo-2H-chromen-4-yl)methanaminium chloride is used as a potential active pharmaceutical ingredient due to its chromen ring structure, which is prevalent in various natural products and pharmaceuticals. (6-methyl-2-oxo-2H-chromen-4-yl)methanaminium chloride's potential biological activities make it a candidate for further research and development in the pharmaceutical field.
Used in Chemical Research:
In the field of chemical research, (6-methyl-2-oxo-2H-chromen-4-yl)methanaminium chloride serves as a subject for investigation into its stability, solubility, and possible interactions with other molecules. Understanding these properties can help researchers explore its potential applications in various chemical processes and reactions.
Used in Material Science:
The unique structure of (6-methyl-2-oxo-2H-chromen-4-yl)methanaminium chloride may offer novel properties that could be beneficial in material science. It can be used as a component in the development of new materials with specific characteristics, such as improved stability or solubility, depending on the requirements of various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 98317-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,3,1 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98317-60:
(7*9)+(6*8)+(5*3)+(4*1)+(3*7)+(2*6)+(1*0)=163
163 % 10 = 3
So 98317-60-3 is a valid CAS Registry Number.
98317-60-3Relevant academic research and scientific papers
Synthesis and Biological Activity of 4-(Sulphonamidomethyl)coumarins
Hanmantgad, Hrikant S.,Kulkarni, Manohar V.,Patil, Vemanna D.
, p. 459 - 461 (2007/10/02)
Various sulphanilamidomethylcoumarins (III a-w) have been synthesised by a four-step route.These sulphonamides have been characterised by their spectral data and some of them show better antibacterial activity against Staph. aureus and Esch. coli than the standard (sulphanilamide).Structure activity relationship has also been studied.
