2876-23-5 Usage
Also Known As
10-Aminophenazine
Chemical Classification
Synthetic organic compound, derivative of phenazine
Physical State
Yellow crystalline solid
Solubility
Insoluble in water, soluble in organic solvents
Common Uses
Reagent in chemical research
Precursor in the synthesis of various organic compounds
Intermediate in the production of dyes, pharmaceuticals, and industrial chemicals
Potential Applications
Materials science
Nanotechnology
Unique Properties
Electronic properties
Optical properties
Check Digit Verification of cas no
The CAS Registry Mumber 2876-23-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2876-23:
(6*2)+(5*8)+(4*7)+(3*6)+(2*2)+(1*3)=105
105 % 10 = 5
So 2876-23-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H9N3/c13-8-5-6-11-12(7-8)15-10-4-2-1-3-9(10)14-11/h1-7H,13H2
2876-23-5Relevant 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.
