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Diethyl(phenylethynyl)phosphine is an organophosphorus compound with the chemical formula C12H13P. It is a colorless liquid at room temperature and is characterized by its unique structure, which includes a phosphorus atom bonded to two ethyl groups and a phenylethynyl group. diethyl(phenylethynyl)phosphine is an important intermediate in the synthesis of various phosphorus-containing organic compounds and is used in the preparation of phosphine ligands for transition metal complexes. Diethyl(phenylethynyl)phosphine is also employed in the production of specialty chemicals, agrochemicals, and pharmaceuticals. Due to its reactivity and potential toxicity, it is essential to handle diethyl(phenylethynyl)phosphine with care and in accordance with proper safety protocols.

7528-15-6

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7528-15-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7528-15-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,2 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7528-15:
(6*7)+(5*5)+(4*2)+(3*8)+(2*1)+(1*5)=106
106 % 10 = 6
So 7528-15-6 is a valid CAS Registry Number.

7528-15-6Relevant academic research and scientific papers

Unprecedented synthesis of alkynylphosphine-boranes through room-temperature oxidative alkynylation

Jouvin, Kevin,Veillard, Romain,Theunissen, Cedric,Alayrac, Carole,Gaumont, Annie-Claude,Evano, Gwilherm

, p. 4592 - 4595 (2013/09/24)

An original and user-friendly synthesis of alkynylphosphine-boranes, useful building blocks in organic synthesis, based on an oxidative P-alkynylation reaction with readily available copper acetylides is reported. The ability of a secondary phosphine protected with a borane to undergo oxidative coupling without oxidation of the P-moiety is demonstrated for the first time. The reaction, which proceeds at room temperature, is applicable to the preparation of enantioenriched and structurally complex alkynylphosphine-boranes.

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