1538-59-6 Usage
Uses
Used in Organic Synthesis:
Triphenylantimony dibromide is used as a catalyst in the production of plastics, resins, and pharmaceuticals. Its catalytic activity facilitates the synthesis of these materials, making it an essential component in the chemical industry.
Used in Flame Retardants:
In some applications, triphenylantimony dibromide is used as a flame retardant to enhance the fire resistance of materials. Its ability to slow down the combustion process makes it a valuable additive in certain industries.
Used in Research and Development:
Due to its unique chemical properties, triphenylantimony dibromide is also utilized in research and development for the discovery of new chemical reactions and the synthesis of novel compounds.
However, it is important to note that triphenylantimony dibromide is a toxic compound that can cause skin and eye irritation. It may also have harmful effects on aquatic life. Therefore, proper handling, storage, and disposal measures should be strictly followed to ensure the safety of both individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 1538-59-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,3 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1538-59:
(6*1)+(5*5)+(4*3)+(3*8)+(2*5)+(1*9)=86
86 % 10 = 6
So 1538-59-6 is a valid CAS Registry Number.
InChI:InChI=1/3C6H5.2BrH.Sb/c3*1-2-4-6-5-3-1;;;/h3*1-5H;2*1H;/q;;;;;+2/p-2/rC18H15Br2Sb/c19-21(20,16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
1538-59-6Relevant academic research and scientific papers
Synthesis and Structure of Triarylantimony Bis(arenesulfonates)
Sharutin,Sharutina,Platonova,Pakusina,Panova,Fukin,Zakharov
, p. 354 - 357 (2007/10/03)
Triarylantimony bis(arenesulfonates) were prepared by reaction of triarylantimonies with hydrogen peroxide in the presence of arenesulfonic acids. The steric structure of the products was assessed. Triarylantimony bis(arenesulfonates) were reacted with so
Structural Investigations of the Organoantimony(V) Halides Ph4SbX and Ph3SbX2 (X = Cl, Br or I) in the Solid State and in Solution
Baker, Lisa-Jane,Rickard, Clifton E. F.,Taylor, Michael J.
, p. 2895 - 2900 (2007/10/03)
X-Ray crystallography revealed a distorted trigonal-bipyramidal structure for Ph4SbI, with Sb-Cax 2.141(3), Sb-Ceq 2.103(3)-2.117(3) Angstroem and a long Sb-I distance of 3.341(1) Angstroem in monoclinic crystals of P21/n symmetry.Consideration of the weak Sb-X bonds in Ph4SbX (X = Cl, Br or I) leads to reassignment of their Raman spectra; Ph4SbI ionises forming (1+) in acetonitrile, as shown by 13C and 121Sb NMR spectra.The halide Ph3SbI2 is reported in two phases, yellow, orthorombic (Fdd2) crystals isomorphous with Ph3SbBr2 and off-white, cubic (P4332) crystals.In each the molecule is trigonal-bipyramidal, with axial Sb-I bonds of 2.865(1) Angstroem in the former and 2.885(1) Angstroem in the latter, and small differences in their respective bond angles.The phenyl groups of the cubic form are in the regular propeller arrangement whereas one group of the orthorhombic form has a reversed orientation.The vibrational spectra of the two forms differ slightly.
