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Diphenyl-(3-oxo-1-phenylbutyl)-phosphin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16247-25-9

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16247-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16247-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,4 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16247-25:
(7*1)+(6*6)+(5*2)+(4*4)+(3*7)+(2*2)+(1*5)=99
99 % 10 = 9
So 16247-25-9 is a valid CAS Registry Number.

16247-25-9Relevant academic research and scientific papers

Rhodium Complexes in P-C Bond Formation: Key Role of a Hydrido Ligand

Varela-Izquierdo, Víctor,Geer, Ana M.,Navarro, Janeth,López, José A.,Ciriano, Miguel A.,Tejel, Cristina

supporting information, p. 349 - 358 (2021/01/13)

Olefin hydrophosphanation is an attractive route for the atom-economical synthesis of functionalized phosphanes. This reaction involves the formation of P-C and H-C bonds. Thus, complexes that contain both hydrido and phosphanido functionalities are of gr

Unsymmetrical chiral PCN pincer palladium(II) and nickel(II) complexes with aryl-based aminophosphine-imidazoline ligands: Synthesis via aryl C-H activation and asymmetric addition of diarylphosphines to enones

Yang, Ming-Jun,Liu, Yan-Jing,Gong, Jun-Fang,Song, Mao-Ping

experimental part, p. 3793 - 3803 (2011/09/20)

Figure Persented: Chiral 3-(2′-imidazolinyl)anilines 3a-c were easily synthesized by converting the carboxyl and nitro groups in commercially available 3-nitrobenzoic acid to chiral imidazoline and amine, respectively. The one-pot phosphorylation/metalati

Dual Radical/Polar Pudovik Reaction: Application Field of New Activation Methods

Semenzin, Delphine,Etemad-Moghadam, Guita,Albouy, Dominique,Diallo, Ousmane,Koenig, Max

, p. 2414 - 2422 (2007/10/03)

The Pudovik reaction (addition of organophosphorus compounds containing a labile P-H bond with alkenes and alkynes) can progess via a radical or (and) ionic mechanism. A comparative and systematic study including various reagents and different activation methods (heating, photochemical or ultrasonic irradiation, and dry medium supported reactions) is presented. Photolysis is the most efficient method for the radical processes, but in a few examples, ultrasonic irradiation can be more appropriate since the reaction time is shorter and ultrasound did not induce side-reactions (in particular Z/E isomerization). Dry medium process on basic solid support is the best anionic activation (yield, time, selectivity, purification facilities). Ultrasound, by its mechanical effects, can contribute to increase yield compared to the classical thermal method under these basic conditions. All the activation methods are efficient whatever the unsaturated substrates for the phosphine reactivity, whereas the appropriate activation method is exclusively determined by the nature of the unsaturated system for the thiophosphine (or phosphine oxide) reactivity.

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