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Tris(2-(methylthio)phenyl)arsane is an organoarsenic compound with the chemical formula C18H15AsS3. It is a colorless, crystalline solid that is soluble in organic solvents. tris(2-(methylthio)phenyl)arsane is characterized by its three phenyl rings, each substituted with a methylthio group at the 2-position and an arsenic atom at the para-position. The arsenic atom is bonded to all three phenyl rings, forming a tris-chelate structure. Tris(2-(methylthio)phenyl)arsane is of interest in organometallic chemistry and may have potential applications in materials science and pharmaceuticals due to its unique structure and properties. However, it is important to note that organoarsenic compounds can be toxic, and their handling should be done with appropriate safety measures.

18281-89-5

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18281-89-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18281-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,8 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18281-89:
(7*1)+(6*8)+(5*2)+(4*8)+(3*1)+(2*8)+(1*9)=125
125 % 10 = 5
So 18281-89-5 is a valid CAS Registry Number.

18281-89-5Upstream product

18281-89-5Downstream Products

18281-89-5Relevant academic research and scientific papers

Carbonylative C?C Bond Activation of Electron-Poor Cyclopropanes: Rhodium-Catalyzed (3+1+2) Cycloadditions of Cyclopropylamides

Dalling, Andrew G.,Yamauchi, Takayuki,McCreanor, Niall G.,Cox, Lydia,Bower, John F.

, p. 221 - 225 (2019)

Rh-catalyzed carbonylative C?C bond activation of cyclopropylamides generates configurationally stable rhodacyclopentanones that engage tethered alkenes in (3+1+2) cycloadditions. These studies provide the first examples of multicomponent cycloadditions t

Trigonal-bipyramidal nickel(II) complexes containing sulfur ligand atoms

Dyer,Meek, Devon W.

, p. 1398 - 1402 (1965)

A new tetradentate ligand, tris(o-methylthiophenyl)phosphine, P(o-C6H4SCH3)3 (TSP, I), forms a series of crystalline, intensely-colored, trigonal-bipyramidal nickel(II) complexes containing the species [Ni(TSP)X]+ (X = I, Br, Cl, or NCS) or [Ni(TSP)L]2+ (L = thiourea, triphenylphosphine, or methyldiphenylphosphine). The two lowest energy electronic absorption bands in the visible and ultraviolet spectra have been assigned to the two 1A, → 1E(D) transitions. Under similar conditions, the analogous arsine compound, tris(o-methylthiophenyl)arsine, As(o-C6H4SCH3)3 (TSA), did not react with nickel(II) salts.

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