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1-Phenyl-3-methyl-3-phospholene 1-sulfide is a complex organic compound with the molecular formula C9H11PS. It is a derivative of phospholene, which is a heterocyclic compound containing a phosphorus atom in a five-membered ring. This specific compound features a phenyl group (C6H5) attached to the 1-position of the phospholene ring, a methyl group (CH3) at the 3-position, and a sulfide group (S) also at the 1-position. The presence of these functional groups imparts unique chemical properties to the molecule, making it a potential candidate for various applications in the fields of organic chemistry, materials science, and pharmaceuticals. Due to its structural complexity, 1-phenyl-3-methyl-3-phospholene 1-sulfide may exhibit interesting reactivity patterns and could be further explored for its potential use in the synthesis of more complex molecules or as a building block in the development of new materials.

5958-61-2

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5958-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5958-61-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,5 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5958-61:
(6*5)+(5*9)+(4*5)+(3*8)+(2*6)+(1*1)=132
132 % 10 = 2
So 5958-61-2 is a valid CAS Registry Number.

5958-61-2Downstream Products

5958-61-2Relevant academic research and scientific papers

The deoxygenation of phosphine oxides under green chemical conditions

Keglevich, Gy?rgy,Kovcs, Tamara,Csatls, Flra

, p. 199 - 205 (2015/05/19)

The deoxygenation of a few diaryl-phenylphosphine oxides, dimethyl-phenylphosphine oxide, and 3-methyl-1-phenyl-3-phospholene 1-oxide was studied by phenylsilane, tetramethyldisiloxane (TMDS), and polymethylhydrosiloxane (PMHS) under conventional or microwave (MW) heating, in toluene or in the absence of any solvent at different temperatures. It was found that the deoxygenation with TMDS or PMHS under MW and solvent-free conditions may be the method of choice and provides a green chemical approach.

Alkylation and cyclopentannulation of phospholene derivatives

Pakulski, Zbigniew,Kwiatosz, Renata,Micha? Pietrusiewicz

, p. 1481 - 1492 (2007/10/03)

The deprotonation of 1-phenyl-3-phospholene 1-oxide, 1-sulfide or 1-borane with 1 or 2 equiv of LDA, followed by quenching with electrophiles gave a range of 2-mono- or 2,5-disubstituted phospholene derivatives in good yield. Only trans substitution in re

Synthesis of functionalized P-heterocycles including phosphine-borane complexes

Keglevich, Gyoergy,Toke, Laszlo,Ujszaszy, Kalman,Szollosy, Aron

, p. 457 - 460 (2007/10/03)

Preparation of phosphinic chlorides, amides, and sulfide derivatives, as well as phosphine-borane complexes of P-heterocycles is described.

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