13711-39-2 Usage
Chemical structure
A derivative of naphthalene with a chlorine atom and an amino group attached to adjacent carbon atoms in the naphthalene ring.
Usage
a. Synthesis of various organic compounds
b. Synthesis of pharmaceuticals
Mutagenic
Capable of causing genetic mutations
Carcinogenic
Known to cause or contribute to the development of cancer
Health risks
Exposure to 1-amino-2-chloronaphthalene should be minimized to avoid potential health risks.
Industrial importance
Versatile chemical compound used in the production of various organic compounds and pharmaceuticals.
Toxicological importance
Recognized for its mutagenic and carcinogenic properties, highlighting the need for proper handling and safety measures.
Check Digit Verification of cas no
The CAS Registry Mumber 13711-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,1 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13711-39:
(7*1)+(6*3)+(5*7)+(4*1)+(3*1)+(2*3)+(1*9)=82
82 % 10 = 2
So 13711-39-2 is a valid CAS Registry Number.
13711-39-2Relevant articles and documents
PHOTOCHEMICAL DECOMPOSITION OF 2-AZIDOPHENAZINE IN ALCOHOLS AND IN THE PRESENCE OF CYANIDE ION
Albini, Angelo,Bettinetti, Gian Franco,Fasani, Elisa,Pietra, Silvio
, p. 13 - 18 (2007/10/02)
The photochemical decomposition of 2-azidophenazine in alcoholic solvents has been investigated. 1-Amino-2-alkoxyphenazines are formed in neutral and (in higher yield and together with 2-amino-1-chlorophenazine) in acidic conditions, while the azepinoquinoxaline 7 is formed in basic conditions.With cyanide ion nucleophilic attack takes place giving 1-amino-2-phenazine carbonitrile.To allow comparison, 2-azidonaphthalene, 2-azidoanthracene and 2-azidoanthraquinone have also been photodecomposed in the conditions in which the most interesting results are obtained from 2-azidophenazine.The mechanism of these reactions is briefly discussed.
