42955-73-7 Usage
General Description
4-Nitroacridine is a chemical compound with the molecular formula C13H8N2O2. It is a derivative of acridine and contains a nitro group, which gives it a yellow color. 4-Nitroacridine is mainly used in the synthesis of dyes, pigments, and pharmaceuticals. It has also been studied for its potential applications in organic light-emitting diodes (OLEDs) and as an antitumor agent due to its reported cytotoxic properties. Additionally, it has been investigated for its antimicrobial and antiviral activities. However, 4-Nitroacridine is also known to be toxic and may cause harm if ingested, inhaled, or absorbed through the skin, and should be handled with caution in a laboratory setting.
Check Digit Verification of cas no
The CAS Registry Mumber 42955-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,5 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42955-73:
(7*4)+(6*2)+(5*9)+(4*5)+(3*5)+(2*7)+(1*3)=137
137 % 10 = 7
So 42955-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H8N2O2/c16-15(17)12-7-3-5-10-8-9-4-1-2-6-11(9)14-13(10)12/h1-8H
42955-73-7Relevant articles and documents
1,2-Dihydro-1-hydroxy-2,3,1-benzodiazaborine Bearing an Acridine Moiety as a Circular Dichroism Probe for Determination of Absolute Configuration of Mono-Alcohols
Shimo, Shunsuke,Takahashi, Kohei,Iwasawa, Nobuharu
supporting information, p. 3790 - 3794 (2019/02/26)
A new chiral probe molecule for mono-alcohols is developed by using 1,2-dihydro-1-hydroxy-2,3,1-benzodiazaborine (DAB) bearing an acridine moiety 1. In the presence of mono-alcohols, DAB 1 forms borate 2 by boronic ester formation, followed by coordination of the acridine moiety to the boron atom. Borate 2 has a chiral center on the boron atom and works as a stereodynamic circular dichroism (CD) probe molecule for chiral mono-alcohols based on the π–π interaction between the acridine moiety and the carbon–carbon unsaturated moiety on mono-alcohols.
