26687-12-7 Usage
Chemical structure
1-acridin-9-yl-3-phenylthiourea is a derivative of acridine, a heterocyclic organic compound, and contains a thiourea group.
Potential applications
The compound has potential biological and pharmaceutical applications.
Cytotoxic and antitumor properties
The presence of an acridine moiety suggests potential for this compound to exhibit cytotoxic and antitumor properties, as acridine derivatives have been studied for their potential as anticancer agents.
Interaction with biological targets
The thiourea group may contribute to the compound's ability to interact with biological targets.
Pharmaceutical drug development
1-acridin-9-yl-3-phenylthiourea is a potential candidate for pharmaceutical drug development.
Further research needed
Further research is needed to fully understand the biological and pharmacological properties of 1-acridin-9-yl-3-phenylthiourea and its potential applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 26687-12-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,8 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26687-12:
(7*2)+(6*6)+(5*6)+(4*8)+(3*7)+(2*1)+(1*2)=137
137 % 10 = 7
So 26687-12-7 is a valid CAS Registry Number.
26687-12-7Relevant articles and documents
KINETICS OF REACTIONS OF 9-ISOTHIOCYANATOACRIDINE WITH AROMATIC AND ALIPHATIC AMINES AND FLUORESCENCE PROPERTIES OF THE 1-ACRIDIN-9-YL-3-ALKYL(ARYL)THIOUREAS OBTAINED
Mazagova, Dana,Kristian, Pavol,Suchar, Gejza,Imrich, Jan,Antalik, Marian
, p. 2632 - 2640 (2007/10/02)
Kinetics of nucleophilic addition reaction of 9-isothiocyanatoacridine with seventeen aliphatic and aromatic amines in organic solvents has been studied by the VIS spectroscopic method. 9-Isothiocyanatoacridine reacted by about two orders of magnitude faster than phenyl isothiocyanate.The reaction rates of aliphatic amines were markedly affected by steric effects.Excepting 1-acridin-9-yl-3-butylthiourea (IIIo), the products obtained exhibited weaker fluorescence than the starting 9-isothiocyanatoacridine.
