71507-04-5 Usage
Derivative of acridine
It is a modified version of the acridine compound, which is an organic compound with a tricyclic structure.
Nitroarenes class
1-Nitro-9-oxo-4-acridinecarboxylic acid belongs to the nitroarenes class of compounds, which are characterized by the presence of a nitro group (-NO2) attached to an aromatic ring.
Bright yellow to orange color
1-Nitro-9-oxo-4-acridinecarboxylic acid is known for its vivid color, which can range from yellow to orange depending on the conditions.
pH indicator
1-Nitro-9-oxo-4-acridinecarboxylic acid changes color in response to pH changes, making it useful for indicating the acidity or alkalinity of a solution.
Organic synthesis
1-Nitro-9-oxo-4-acridinecarboxylic acid is used in organic synthesis, which involves the formation of new chemical bonds and the transformation of chemical structures.
Precursor for pharmaceuticals and dyes
1-Nitro-9-oxo-4-acridinecarboxylic acid serves as a starting material for the production of various pharmaceuticals and dyes, showcasing its versatility in chemical applications.
Potential anti-tumor and anti-bacterial properties
Research has been conducted on 1-Nitro-9-oxo-4-acridinecarboxylic acid for its possible use in treating tumors and bacterial infections, highlighting its potential for medicinal applications.
Importance in organic chemistry
Due to its chemical properties and potential applications, 1-Nitro-9-oxo-4-acridinecarboxylic acid is a significant and versatile chemical in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 71507-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,0 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71507-04:
(7*7)+(6*1)+(5*5)+(4*0)+(3*7)+(2*0)+(1*4)=105
105 % 10 = 5
So 71507-04-5 is a valid CAS Registry Number.
71507-04-5Relevant academic research and scientific papers
Synthesis of Substituted 9-Oxo-9,10-dihydroacridine-4-carboxylic Acids. I. Factors Affecting the Direction of Ring Closure of Substituted N-(2-Carboxyphenylamino)benzoic Acids
Stewart, Georgina M.,Rewcastle, Gordon W.,Denny, William A.
, p. 1939 - 1950 (2007/10/02)
The cyclodehydration of 16 substituted N-(2-carboxyphenylamino)benzoic acids to substituted 9-oxo-9,10-dihydroacridine-4-carboxylic acids with conc.H2SO4, POCl3 and ethyl polyphosphate (epp) has been studied by h.p.l.c.Direction of ring closure can be qua
