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(4-methylphenylthio)diphenylphosphane, also known as 4-methylphenylthio-diphenylphosphane, is an organophosphorus compound characterized by a phosphorus atom bonded to two phenyl groups and a 4-methylphenylthio group. (4-methylphenylthio)diphenylphosphan is a colorless solid with a molecular formula of C19H17PS. It is an important intermediate in the synthesis of various organophosphorus compounds, such as pesticides and flame retardants, due to its unique structure and reactivity. The compound is also used in the preparation of ligands for transition metal complexes, which have applications in catalysis and materials science. Its chemical properties include reactivity towards nucleophiles and electrophiles, making it a versatile building block in organic synthesis.

58558-57-9

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58558-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58558-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,5 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58558-57:
(7*5)+(6*8)+(5*5)+(4*5)+(3*8)+(2*5)+(1*7)=169
169 % 10 = 9
So 58558-57-9 is a valid CAS Registry Number.

58558-57-9Relevant academic research and scientific papers

Visible-Light-Promoted Photoredox Dehydrogenative Coupling of Phosphines and Thiophenols

Wang, Xianya,Xia, Chungu,Wu, Lipeng

, p. 7373 - 7377 (2020)

Herein, by applying visible-light photoredox catalysis, we have now achieved the first example of catalytic dehydrogenative coupling of phosphines and thiophenols that proceeds at room temperature. Key to our success is the use of benzaldehyde as a soft oxidant, which avoids the issue of phosphine oxidation. Furthermore, we observed the unexpected dealkylative coupling of secondary and tertiary alkylphosphine with thiophenols.

Metal-free electrophilic phosphination of electron-rich arenes, arenols and aromatic thiols with diarylphosphine oxides

Yuan, Tao,Huang, Shenlin,Cai, Chun,Lu, Guo-Ping

supporting information, p. 30 - 33 (2017/12/27)

A new protocol for achieving the phosphination of arenes, arenols and thiols has been disclosed. This chemistry, in which diaryl(((trifluoromethyl)sulfonyl)oxy)phosphines as a kind of electrophilic phosphination reagents are in situ generated from diarylp

The Kinetics and Mechanism of the Reaction of Tricoordinate Phosphorus Compounds with Diaryl Trisulfides

Hall, C. Dennis,Tweedy, Bruce R.,Kayhanian, Robert,Lloyd, John R.

, p. 775 - 779 (2007/10/02)

Kinetic data and activation parameters are reported for the reaction of a series of tricoordinate phosphorus compounds, , with diaryl trisulfides.The second-order rate coefficients for series of arylphosphines, phosphinites and phosphonites, correlate with the Hammett ? constants of the aryl substituents with ρ values of -1.1, -1.1 and -1.1 respectively and these results are discussed in terms of a biphilic mechanism analogous to that proposed for the reaction of tricoordinate phosphorus with S8.

SYNTHESE VON BIS(ALKYLTRITHIOCARBONATO)ORGANYL- UND MONO(ALKYLTRITHIOCARBONATO)- DIORGANYL-PHOSPHANEN

Wieber, Markus,Bauer, Bernd

, p. 93 - 98 (2007/10/02)

Compounds of the type RP(S2CSR')2 with R=CH3, C(CH3)3, C6H5 and of the type R2PS2CSR' with R=C(CH3)3, C6H5; R'=C2H5, CH(CH3)2 are obtained by reaction of organylchlorophosphanes with sodium alkyl trihiocarbonates.Ir, NMR and mass spectra have been assigned.

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