7461-24-7 Usage
Uses
Used in Organic Synthesis:
(1E)-2,3-dihydro-1H-inden-1-one semicarbazone is used as a reagent in organic synthesis for the preparation of various heterocyclic compounds. Its unique structure allows it to participate in a range of chemical reactions, contributing to the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
(1E)-2,3-dihydro-1H-inden-1-one semicarbazone is used as a compound with potential pharmacological activities in pharmaceutical research. Its antimicrobial and anti-inflammatory properties make it a candidate for the development of new therapeutic agents.
Used in Antimicrobial Applications:
In the field of antimicrobial applications, (1E)-2,3-dihydro-1H-inden-1-one semicarbazone is used for its potential to combat various microorganisms, which could be beneficial in the development of new antibiotics or antifungal agents.
Used in Anti-inflammatory Applications:
(1E)-2,3-dihydro-1H-inden-1-one semicarbazone is also used in anti-inflammatory applications due to its potential to reduce inflammation, which may lead to its use in the treatment of inflammatory diseases.
Used in Therapeutic Agent Development:
(1E)-2,3-dihydro-1H-inden-1-one semicarbazone is used as a starting point for the development of therapeutic agents for various diseases, given its pharmacological potential and the ongoing research into its properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 7461-24-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7461-24:
(6*7)+(5*4)+(4*6)+(3*1)+(2*2)+(1*4)=97
97 % 10 = 7
So 7461-24-7 is a valid CAS Registry Number.
7461-24-7Relevant academic research and scientific papers
Dimmock, J. R.,Pandeya, S. N.,Quail, J. W.,Pugazhenthi, U.,Allen, T. M.,et al.
, p. 303 - 314 (1995)
A number of aryl alicyclic ketones were converted to their corresponding semicarbazones, thiosemicarbazones and bis-carbohydrazones.Anticonvulsant activity was displayed by most of the compounds in the maximal electroshock (MES) and subcutaneous pentylenetetrazole (scPTZ) screens when given intraperitoneally to mice.However, on oral administration to rats, a marked selective activity in the MES screen only was noted.X-ray crystallography on five semicarbazones was undertaken in order to find correlations between the shapes of these molecules and anticonvulsant properties.The thiosemicarbazones displayed greater cytotoxicity to P388D1 and L1210 cells than the semicarbazones while a number of human tumors and different viruses were, in general, insensitive to representative compounds.semicarbazone/ thiosemicarbazone/ anticonvulsant agent/ X-ray crystallography/ cytotoxic agent
