26223-16-5 Usage
Chemical structure
A heterocyclic organic compound containing a five-membered ring with three nitrogen atoms and one selenium atom.
Family
A member of the selenadiazole family.
Structural similarity
Similar to other nitrogen-containing heterocycles such as pyrazole and triazole.
Chemical and biological properties
Exhibits a range of interesting chemical and biological properties.
Field of interest
A topic of interest in medicinal chemistry and material science.
Potential applications
a. Building block in the synthesis of novel pharmaceuticals.
b. Ligand in coordination chemistry.
Potential applications
Has potential applications in various fields, including pharmaceuticals and materials science.
Investigated properties
a. Antioxidant properties.
b. Anti-cancer properties.
Versatility
A versatile compound in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 26223-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,2 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26223-16:
(7*2)+(6*6)+(5*2)+(4*2)+(3*3)+(2*1)+(1*6)=85
85 % 10 = 5
So 26223-16-5 is a valid CAS Registry Number.
26223-16-5Relevant articles and documents
2-METHYLENE-1,3-DISELENOLE:A PRECURSOR OF TETRASELENAFULVALENE (TSeF)
Jackson, Yvette A.,White, Christy L.,Lakshmikantham, M. V.,Cava, Michael P.
, p. 5635 - 5636 (1987)
The preparation of methylene-1,3-diselenole and its ready conversion to TSeF are discussed.
Synthesis of sym-(E/Z)-Diselenadithiafulvalene
Lakshmikantham, M.V.,Cava, Michael P.
, p. 2632 - 2636 (2007/10/02)
sym-Diselenadithiafulvalene (3) has been synthesized as an inseparable E,Z isomer mixture by two fundamentally different routes.The first synthesis proceeds via ethylene diselenocyanate (9), ethane-1,2-diselenol (8), 1,3-Diselenolane-2-thione (7), 4,5-bis(carbomethoxy)-1,3-thiaselenole-2-selone (12),and tetrakis(carbomethoxy)-sym-diselenadithiafulvalene (13).The second synthesis,which involves a greatly improved route to 1,3-thiaselenole-2-selone (18),provides the most practical method available for the preparation of larger quantities of 3.
