1538-63-2 Usage
Uses
Used in Organic Synthesis:
Chloro(triphenyl)-lambda~5~-stibanyl hydrate is used as a reagent for facilitating various chemical reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its unique structure and properties make it a valuable component in the synthesis of complex organic molecules.
Used in Coordination Chemistry:
Chloro(triphenyl)-lambda~5~-stibanyl hydrate is used as a ligand in coordination chemistry. Its ability to form stable complexes with metal ions makes it a useful component in the development of new coordination compounds with potential applications in various fields.
Used in Catalysis:
Chloro(triphenyl)-lambda~5~-stibanyl hydrate has been studied for its potential applications in catalysis. Its ability to facilitate chemical reactions makes it a promising candidate for use as a catalyst in various industrial processes.
Used as a Precursor for Organostibine Compounds:
Chloro(triphenyl)-lambda~5~-stibanyl hydrate is used as a precursor for the synthesis of other organostibine compounds. Its unique structure and reactivity make it a valuable starting material for the development of new organostibine compounds with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1538-63-2 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, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1538-63:
(6*1)+(5*5)+(4*3)+(3*8)+(2*6)+(1*3)=82
82 % 10 = 2
So 1538-63-2 is a valid CAS Registry Number.
1538-63-2Relevant academic research and scientific papers
Structural characterization of some novel oxidation products of triphenylstibine
Effendy,Grigsby, Warren J.,Hart, Robert D.,Raston, Colin L.,Skelton, Brian W.,White, Allan H.
, p. 675 - 681 (2007/10/03)
Room-temperature single-crystal X-ray structural characterizations of two oxidation products of triphenylstibine of the form XPh3SbOSbPh3X are recorded for X = Cl, NO3. ClPh3SbOSbPh3Cl is monoclinic, P21/c, Z = 4 f.u., a 9.109(4), b 19.809(8), c 19.30(2) A, β 109.27(5)°, conventional R on |F| being 0.038 for No 4431 'observed' (I > 3σ(I)) independent reflections. In this complex, Sb-O-Sb is quasi-linear, 173.1(3)°, in contrast to the previously recorded benzene solvate, in which it is 139.0(3)°; in the nitrate, [(O2NO)Ph3SbOSbPh3(ONO2)], triclinic, P1, Z = 2 f.u., a 15.609(5), b 13.238(4), c 10.140(2) A, α 87.11(2), β 88.46(7), γ 72.93(2)°, R 0.036 for No 5275, it is also bent (137.0(2)°). The anionic substituent is opposed to the oxo bridge in the trigonal bipyramidal five-coordinate array about the metal in both complexes. A redetermination of the structure of Ph8Sb4O6 is recorded, presenting a non-disordered model in a triclinic P1 cell, a 19.698(3), b 11.635(2), c 9.739(2) A, α 92.28(1), β 98.98(1), γ 99.74(1)°, Z = 2 f.u., R 0.046 for No 3578. A new ('β') phase of triphenylstibine, crystallized from hexane/toluene is also recorded: monoclinic, P21/c, a 15.386(8), b 11.304(5), c 19.078(8) A, β 111.64(4)°, Z = 8, R 0.045 for No 3393.
