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Silanediamine, N,N',1,1-tetraphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15403-12-0

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15403-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15403-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,0 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15403-12:
(7*1)+(6*5)+(5*4)+(4*0)+(3*3)+(2*1)+(1*2)=70
70 % 10 = 0
So 15403-12-0 is a valid CAS Registry Number.

15403-12-0Relevant academic research and scientific papers

Si-N Heterodehydrocoupling with a Lanthanide Compound

Cibuzar, Michael P.,Waterman, Rory

supporting information, p. 4395 - 4401 (2019/01/03)

[La{N(SiMe3)2}3THF2] (1) is an effective precatalyst for the heterodehydrocoupling of silanes and amines. Coupling of primary and secondary amines with aryl silanes was achieved with a loading of 0.8 mol % of [L

Alkaline-Earth-Catalysed Cross-Dehydrocoupling of Amines and Hydrosilanes: Reactivity Trends, Scope and Mechanism

Bellini, Clément,Dorcet, Vincent,Carpentier, Jean-Fran?ois,Tobisch, Sven,Sarazin, Yann

, p. 4564 - 4583 (2016/03/22)

Alkaline-earth (Ae=Ca, Sr, Ba) complexes are shown to catalyse the chemoselective cross-dehydrocoupling (CDC) of amines and hydrosilanes. Key trends were delineated in the benchmark couplings of Ph3SiH with pyrrolidine or tBuNH2. Ae{

Catalytic dehydrogenative Si-N coupling of pyrroles, indoles, carbazoles as well as anilines with hydrosilanes without added base

K?nigs, C. David F.,Müller, Maria F.,Aiguabella, Nuria,Klare, Hendrik F. T.,Oestreich, Martin

supporting information, p. 1506 - 1508 (2013/03/13)

A base-free, catalytic protocol for the dehydrogenative Si-N coupling of weakly nucleophilic N-H groups of heteroarenes or aryl-substituted amines with equimolar amounts of hydrosilanes is reported. Cooperative Si-H bond activation at a Ru-S bond generates a silicon electrophile that forms a Si-N bond prior to the N-H deprotonation by an intermediate Ru-H complex, only releasing H 2. The Royal Society of Chemistry 2013.

New diazasilaphosphetidines and their precursors

Eichhorn, Bettina,Noeth, Heinrich

, p. 352 - 360 (2007/10/03)

A series of aminosilanes (R′HN)2SiR2 have been prepared. In case of bulky substituents R1 the aminolysis of Ph2SiCl2 stops at the (R′HN)ClSiPh2 stage. Replacement of the Cl atom is achieved with LiNHR′ which allows the synthesis of mixed bisaminosilanes (R′HN)(R″HN)SiPh2. The X-ray structures of three of these compounds have been determined. There are no intermolecular N-H...N hydrogen bonds in these compounds in the solid state. Several 1,3,2,4-diazaphosphetidines have been synthesized using bis(N-lithioamino)silanes and bis(N-lithioamino)phosphanes . Amongst these the heterocycle 18 possesses an almost planar four membered N2SiP ring system.

Synthesis and application of some dianilinosilanes, bis (trimethylsilyl) phenylenediamines and dialkyl benzo-1,3,2-diazasilolines as antioxidants

Ali, Hussein M.,El-Qurashi, Mohamed A. M.

, p. 521 - 529 (2007/10/03)

A number of dialkyl or diphenyl dianilinosilanes, bis (trimethylsilyl) phenylenediamines and dialkyl benzo-1,3,2-diazasilolines were synthesized and used as antioxidants for lubricating base oils. Thermal analysis methods (DSC, TG and DTG) and IR techniqu

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