118947-63-0 Usage
Uses
Used in Coordination Chemistry:
[(3-cyano-6,3'-bipyridin-2-yl)sulfanyl]acetic acid is used as a ligand for forming coordination complexes with metal ions. The presence of the sulfanyl group allows for the creation of stable complexes, which can be useful in various chemical and material applications.
Used in Organic Synthesis:
[(3-cyano-6,3'-bipyridin-2-yl)sulfanyl]acetic acid is used as a versatile building block in organic synthesis. The cyano group can participate in nucleophilic substitution reactions, enabling the synthesis of a wide range of organic compounds with different functional groups.
Used in Pharmaceutical Industry:
[(3-cyano-6,3'-bipyridin-2-yl)sulfanyl]acetic acid has potential applications in the pharmaceutical industry, where it can be used as a starting material for the development of new drugs. Its unique structure and reactivity make it a promising candidate for the synthesis of bioactive molecules with potential therapeutic properties.
Used in Material Science:
In the field of material science, [(3-cyano-6,3'-bipyridin-2-yl)sulfanyl]acetic acid can be used to develop new materials with specific properties. The ability of the compound to form coordination complexes with metal ions can be exploited to create materials with tailored characteristics, such as improved conductivity or magnetic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 118947-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,9,4 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 118947-63:
(8*1)+(7*1)+(6*8)+(5*9)+(4*4)+(3*7)+(2*6)+(1*3)=160
160 % 10 = 0
So 118947-63-0 is a valid CAS Registry Number.
118947-63-0Relevant academic research and scientific papers
CYCLIZATION REACTIONS OF NITRILS. 29. REGIOSELECTIVE SYNTHESIS OF 6-ARYL-3-CYANO-2(1H)-PYRIDINETHIONES AND THE CORRESPONDING SELENONES AND THEIR CHARACTERISTICS
Rodinovskaya, L.A.,Sharanin, Yu.A.,Shestopalov, A.M.,Litvinov, V.P.
, p. 658 - 664 (2007/10/02)
The condensation of cyanothio- and cyanoselenoacetamide with 3-aryl-3-oxo-1-piperidino-1-propene or sodium 3-aryl-3-oxo-1-propen-1-olate takes place regioselectively with the formation of the 6-aryl-3-cyano-2(1H)-pyridinethiones or the corresponding selenones.Thienopyridines, thiazolopyridinium salts, and other annellated heterocycles were obtained from the 6-aryl-3-cyano-2(1H)-pyridinethiones.
