23043-60-9 Usage
Type of compound
Heterocyclic compound
Structure
Planar
Function
Intercalates with DNA
Use
Staining and visualizing cellular nuclei and DNA in biological samples
Fluorescence
Emits blue fluorescence when bound to DNA
Detection
Detected and visualized under a fluorescence microscope
Applications
Molecular biology, cell imaging studies, fluorescence in situ hybridization (FISH), and immunofluorescence assays
Versatility
Can be used in combination with other dyes and stains for multi-color labeling of cellular components
Importance
A widely used tool for studying the structure and function of DNA and cellular nuclei in biological research.
Check Digit Verification of cas no
The CAS Registry Mumber 23043-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,4 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 23043-60:
(7*2)+(6*3)+(5*0)+(4*4)+(3*3)+(2*6)+(1*0)=69
69 % 10 = 9
So 23043-60-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H11N3/c14-9-5-3-7-11-12(9)13(15)8-4-1-2-6-10(8)16-11/h1-7H,14H2,(H2,15,16)
23043-60-9Relevant articles and documents
REDUCTION OF THE ANTICANCER DRUG "NITRACRINE". ACCESS TO DIHYDROPYRAZOLO- AND DIHYDROPYRIMIDINO-ACRIDINES
Cholody, W. M.,Lhomme, M. F.,Lhomme, J.
, p. 5029 - 5032 (1987)
Reduction of the anticancer drug nitracrine 1 leads to the dihydropyrazoloacridine 3 by heterocyclisation.New dihydropyrimidinoacridines 8, 9 and 10 are also described.