7497-52-1 Usage
Uses
Used in Anticancer Applications:
2-Chloroacridin-9(10H)-one is used as an anticancer agent for its in vitro activity against Ehrlich Ascites Carcinoma (EAC) cells. Its acridone structure contributes to its potential as a therapeutic compound in cancer treatment, targeting and inhibiting the growth of cancer cells.
Used in Fluorescent Markers:
As a fluorescent molecule, 2-chloroacridin-9(10H)-one can be used as a marker in various research and diagnostic applications. Its fluorescence property allows for the detection and tracking of specific biological processes or molecules of interest.
Used in Pharmaceutical Research:
2-Chloroacridin-9(10H)-one's unique chemical structure and properties make it a valuable compound for further research and development in the pharmaceutical industry. It can be used as a starting point for the synthesis of new drugs or as a tool to study the mechanisms of action of existing medications.
Used in Analytical Chemistry:
The fluorescent nature of 2-chloroacridin-9(10H)-one can be utilized in analytical chemistry for the detection and quantification of specific substances. It can be employed as a probe or label in various analytical techniques, such as high-performance liquid chromatography (HPLC) or mass spectrometry (MS), to enhance the sensitivity and specificity of these methods.
Check Digit Verification of cas no
The CAS Registry Mumber 7497-52-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7497-52:
(6*7)+(5*4)+(4*9)+(3*7)+(2*5)+(1*2)=131
131 % 10 = 1
So 7497-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H8ClNO/c14-8-5-6-12-10(7-8)13(16)9-3-1-2-4-11(9)15-12/h1-7H,(H,15,16)
7497-52-1Relevant academic research and scientific papers
Isolation and structure elucidation of novel products of the acidic degradation of diazepam
Nudelman,De Waisbaum
, p. 208 - 211 (2007/10/02)
The acidic degradation of diazepam in methanolic aqueous solution has been investigated. Apart from the known degradation products, 2-(N-methylamino)- 5-chlorobenzophenone and glycine, produced by the hydrolytic cleavage of the benzodiazepinone ring, five novel products were isolated and fully characterized by their spectroscopic features and independent synthesis. Substituted 2-amino-3,5-dichlorobenzophenones and 2,4-dichloroacridinones were found, the formation of which in the reaction media is mechanistically intriguing. The rule of these unexpected products in accelerated studies of diazepam stability is discussed.
