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Phosphinic amide, N,N-dimethyl-P,P-bis(trifluoromethyl)-, also known as bis(trifluoromethyl)-N,N-dimethylphosphinic amide, is a chemical compound with the molecular formula C3H3F6NP. It is a colorless liquid at room temperature and is soluble in common organic solvents. phosphinic amide, N,N-dimethyl-P,P-bis(trifluoromethyl)- is an important reagent in organic synthesis, particularly in the formation of carbon-phosphorus bonds and as a ligand in transition metal-catalyzed reactions. It is also used as a precursor for the synthesis of various phosphorus-containing compounds, such as phosphine oxides and phosphinates. Due to its unique structure and reactivity, bis(trifluoromethyl)-N,N-dimethylphosphinic amide has attracted significant interest in the field of organophosphorus chemistry and has potential applications in the development of new pharmaceuticals and agrochemicals.

3331-12-2

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3331-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3331-12-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,3 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3331-12:
(6*3)+(5*3)+(4*3)+(3*1)+(2*1)+(1*2)=52
52 % 10 = 2
So 3331-12-2 is a valid CAS Registry Number.

3331-12-2Relevant academic research and scientific papers

Some reactions of bis(trifluoromethyl)phosphines, -phosphine oxides, and -phosphine sulfides with alcohols and mercaptans. Preparation, characterization, and NMR spectra of a homologous series of esters and thioesters

Cavell, Ronald G.,Pinkerton, A. Alan,Sim, William,Tomlinson, Adrian J.

, p. 2901 - 2908 (2007/10/12)

The esters (CF3)2POR and thioesters (CF3)2PSR (R = CH3, C2H5, CH(CH3)2, and C(CH3)3) of trivalent phosphorus have been synthesized. Previously unknown esters in the series have been characterized and NMR parameters of all the above esters recorded. Synthesis of phosphinous esters and thioesters is aided by the presence of amine which is mandatory in the case of the reaction of tert-butyl alcohol with (CF3)2PCl. In the absence of amine, (CF3)2PCl reacted with tert-butyl alcohol to give (CF3)2P(O)C(CH3)3 and HCl. Separate reactions showed that (CF3)2POC(CH3)3 reacted with HCl to yield (CF3)2POH and (CH3)3CCl and that (CF3)2POH and (CH3)3CCl reacted to form (CF3)2P(O)C(CH3)3 and HCl. These reactions provide a basis for the detailed understanding of the reaction of (CF3)2PCl and related systems with tert-butyl alcohol. The oxy- and thioesters of pentavalent phosphorus, (CF3)2P(O)OR, (CF3)2P(O)SR, (CF3)2P(S)OR, and (CF3)2P(S)SR (R = CH3, C2H5, CH(CH3)2), were prepared by reactions analogous to those used to prepare the phosphinous esters; however, the competitive reaction of salt formation with amines in the case of the tert-butyl and, to a lesser extent, methyl esters requires use of alternate synthetic routes. In the case of tert-butyl esters, isobutene was also obtained in addition to the amine salt due to the instability of the tert-butylammonium salt. The tert-butyl thioester (CF3)2P(S)SC(CH3)3 was obtained from tert-butyl iodide and the appropriate phosphorus acid salt, (CF3)2PS2-. In contrast the dioxo and oxythioesters could not be prepared in this way. NMR parameters are recorded for all esters of pentavalent phosphorus and the new esters of pentavalent phosphorus have been characterized. Separate reaction of the esters of pentavalent phosphorus with trimethylamine gave R′(CH3)3N+(CF3) 2PXY- (X, Y = O, S) salts. In the case of esters of trivalent phosphorus, only (CF3)2POCH3 formed a 1:1 adduct with trimethylamine which may be the salt (CH3)4N+(CF3)2PO - NMR parameters of the tert-butylphosphine oxide (CF3)2P(O)C4H4 are also given.

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