3411-49-2 Usage
Uses
Used in Coordination Chemistry:
Trinaphthalen-1-ylphosphane sulfide is used as a ligand for the synthesis of organophosphorus compounds, leveraging its strong electron-donating properties to form stable complexes with transition metals.
Used in Chemical Reactions:
Due to its high thermal stability and resistance to oxidation, trinaphthalen-1-ylphosphane sulfide is used as a valuable reagent in various chemical reactions, enhancing the efficiency and selectivity of the processes.
Used in Catalysis:
Trinaphthalen-1-ylphosphane sulfide is employed in catalysis, where its unique properties can improve the performance of catalytic systems, potentially leading to more effective and sustainable chemical transformations.
Used in Materials Science:
trinaphthalen-1-ylphosphane sulfide is also studied for its potential applications in materials science, where it could contribute to the development of new materials with enhanced properties, such as improved conductivity or stability.
Check Digit Verification of cas no
The CAS Registry Mumber 3411-49-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,1 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3411-49:
(6*3)+(5*4)+(4*1)+(3*1)+(2*4)+(1*9)=62
62 % 10 = 2
So 3411-49-2 is a valid CAS Registry Number.
3411-49-2Relevant academic research and scientific papers
Polarity and Conformational Analysis of Tri(1-naphthyl)phosphine, Tri(2-naphthyl)phosphine, and Their Chalcogenides
Kuznetsova,Chachkov,Belogorlova,Kuimov,Malysheva,Vereshchagina, Ya. A.
, p. 1245 - 1255 (2021/09/30)
Abstract: The polarity and structure of tri(1- or 2-naphthyl)phosphines and their chalcogenides were determined by the methods of dipole moments, IR spectroscopy, and DFT quantum-chemical calculations at the B3PW91/6-311++G(df,p) level of theory. In solution, tri(1-naphthyl)phosphine prefers a single conformer with a gauche,gauche,gauche orientation of the substituents at the phosphorus. Tri(2-naphthyl)phosphine, as well as both phosphine chalcogenides exist as equilibrium mixtures of several forms with a propeller arrangement of the substituents and a cis or gauche orientation of the Csp2?Csp2 and P=X (X = LEP, O, S, Se) bonds.
X-ray structures and oxidative electrochemistry of phosphine sulfides and phosphine selenides
Tiedemann, Margaret A.,Mandell, Chelsea L.,Chan, Benny C.,Nataro, Chip
, p. 193 - 201 (2015/01/08)
A variety of mono- and bisphosphine sulfides and selenides were synthesized and structurally characterized by NMR spectroscopy. In addition, the X-ray crystal structures were determined for eleven of these compounds. The percent buried volume was determin
