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Diphenylphosphino-N-phenyl(thioformamido)triphenyltin is a complex organotin compound with the chemical formula C36H30NPSn. It is characterized by a central tin (Sn) atom, which is bonded to three phenyl groups and a diphenylphosphino-N-phenyl(thioformamido) ligand. The ligand itself consists of a diphenylphosphino group, a phenyl group, and a thioformamido group. {diphenylphosphino-N-phenyl(thioformamido)}triphenyltin is of interest in organometallic chemistry and may have potential applications in various fields, such as catalysis and material science, due to its unique structure and properties.

4546-00-3

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4546-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4546-00-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,4 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4546-00:
(6*4)+(5*5)+(4*4)+(3*6)+(2*0)+(1*0)=83
83 % 10 = 3
So 4546-00-3 is a valid CAS Registry Number.

4546-00-3Downstream Products

4546-00-3Relevant academic research and scientific papers

Investigation of Isomer Formation of Triorganotin(IV) Complexes Involving Diorganophosphino-N-phenyl(thioformamide) Ligands: The Crystal and Molecular Structure of triphenyltin, Ph3Sn

Dakternieks, Dainis,Hoskins, Bernard F.,Rolls, Carolyn L.

, p. 195 - 202 (2007/10/02)

The isomer of Ph3Sn formed depends on the method of preparation.The crystal and molecular structure of the tin(IV) complex Ph3Sn has been established by single-crystal X-ray diffraction technique.The crystals are monoclinic, space group P21/n, a 12.620(2), b 10.541(2), c 24.294(4) Angstroem, β 96.90(1) with Z 4; R and Rw were 0.031 and 0.034 respectively for 5632 unique reflections with I 3?(I).The crystals consist of discrete Ph3Sn molecules.There is a tetrahedral environment about the tin atom formed by the three phenylic carbons and a sulfur atom of the - ligand.Comparisons are made with the structurally similar compound Ph3Sn.On the basis of these comparisons and on earlier n.m.r. data, a favoured four-centered mechanism for insertion of dipolar PhNCS into the tin-phosphorus bond of Ph3SnPPh2 is inferred.Differences in reactivity of Ph2PC(S)N(H)Ph and (c-C6H11)2PC(S)N(H)Ph appear to result from electronic rather than steric effects.

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