65456-35-1 Usage
General Description
5-(4-chlorophenyl)-1,3-thiaselenole-2-thione, also known as 4-Chlorophenyl-1,3-benzisoselenazol-2(3H)-thione, is a chemical compound belonging to the class of organoselenium compounds. It contains a thiaselenole ring, which is a five-membered heterocycle containing both a selenium and a sulfur atom. 5-(4-chlorophenyl)-1,3-thiaselenole-2-thione has potential applications in the field of organic synthesis and medicinal chemistry due to its unique structure and reactivity. It may have pharmacological properties and can be used as a building block for the synthesis of more complex organic molecules. Additionally, it may have potential as a starting material for the development of new materials and pharmaceuticals. Further research is needed to fully understand the potential uses and properties of 5-(4-chlorophenyl)-1,3-thiaselenole-2-thione.
Check Digit Verification of cas no
The CAS Registry Mumber 65456-35-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,5 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65456-35:
(7*6)+(6*5)+(5*4)+(4*5)+(3*6)+(2*3)+(1*5)=141
141 % 10 = 1
So 65456-35-1 is a valid CAS Registry Number.
65456-35-1Relevant academic research and scientific papers
UNSATURATED THIOLATES AND THEIR ANALOGS IN CYCLOADDITION REACTIONS. XIII. REACTIONS OF POTASSIUM 2-ARYL- AND 2-ALKYLETHYNESELENOLATES WITH HETEROCUMULENES
Laishev, V. Z.,Petrov, M. L.,Petrov, A. A.
, p. 450 - 454 (2007/10/02)
Potassium 2-aryl- and 2-alkylethyneselenolates, obtained by the decomposition of 4-substituted 1,2,3-selenadiazoles, enter into a cyclization reaction with phenyl isothiocyanate to form isomeric N-(5-R-1,3-thiaselenol-2-ylidene)phenylamines.Measurement of the relative rate constants for cyclization of 2-(p-R-aryl)ethyneselenolates at the thione bond shows that the reaction is accelerated by donating substituents and retarded by withdrawing substituents.
