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Phenyl-phenylethinyl-phosphinigsaeure-diethylamid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

146286-07-9

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146286-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146286-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,2,8 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 146286-07:
(8*1)+(7*4)+(6*6)+(5*2)+(4*8)+(3*6)+(2*0)+(1*7)=139
139 % 10 = 9
So 146286-07-9 is a valid CAS Registry Number.

146286-07-9Relevant academic research and scientific papers

Experimental and DFT study of the tautomeric behavior of cobalt-containing secondary phosphine oxides

Wei, Chu-Hung,Wu, Cheng-En,Huang, Yi-Luen,Kultyshev, Roman G.,Hong, Fung-E.

, p. 1583 - 1593 (2007)

New cobalt-containing secondary phosphine oxides [(μ-PPh 2CH2PPh2)Co2(CO)4{μ, η-PhC≡C-P(=O)(H)(R)}] (8a: R = tBu; 8b: R = Ph) were prepared by reaction of secondary phosphine oxides PhC≡CP-(=O)(H)(R)

First Synthesis of Secondary P-Alkenyl and P-Alkynyl Phosphine Oxides

Baba, Gnon,Pilard, Jean-Francois,Tantaoui, Khalid,Gaumont, Annie-Claude,Denis, Jean-Marc

, p. 4421 - 4424 (2007/10/02)

A general method for preparing secondary P-alkenyl and P-alkynyl phosphine oxides, compounds unknown so far, involves the condensation of the vinyl Grignard reagent or lithium acetylide on P-chloroaminophosphines followed by acidic hydrolysis of the corresponding vinyl or ethynylaminophosphines on a solid acid (Amberlyst 15).The few reported chemical properties are mainly related to the strong PH bond activation.Of special interest is the addition of a secondary vinylphosphine oxide derivative on methyl acrylate which occurs at room temperature without any catalyst.

THIAZAPHOSPHOLIDINE. IV. THIAZAPHOSPHOLIDINSULFIDE UND -OXIDE, ETHINYLAMINOPHOSPHANE

Fluck, Ekkehard,Bieger, Klaus,Heckmann, Gernot,Weller, Frank,Boegge, Hartmut

, p. 59 - 78 (2007/10/02)

The synthesis of the ethinylaminophosphanes 1-5 from substituted alkinylmagnesium bromides and halogenoaminophosphanes is described.Reaction of 1 with various derivatives of urea yields the thiazaphospholidines 6, 7, 11-13, 2 reacts with thiouracil

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