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349545-06-8

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349545-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 349545-06-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,9,5,4 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 349545-06:
(8*3)+(7*4)+(6*9)+(5*5)+(4*4)+(3*5)+(2*0)+(1*6)=168
168 % 10 = 8
So 349545-06-8 is a valid CAS Registry Number.

349545-06-8Downstream Products

349545-06-8Relevant academic research and scientific papers

Synthesis and X-ray Crystal Structures of Ga-substituted Distibenes [L(X)GaSb]2

Krüger, Julia,Schoening, Juliane,Ganesamoorthy, Chelladurai,John, Lukas,W?lper, Christoph,Schulz, Stephan

, p. 1028 - 1033 (2018)

The reactions of two equivalents of LGa {L = HC[C(Me)N(2,6-iPr2C6H3)]2} with SbX3 (X = Br, I, OEt) proceed with elimination of LGaX2 and formation of Ga-substituted distibenes [L(X)GaSb]su

Addressing the chemical sorcery of "GaI": Benefits of solid-state analysis aiding in the synthesis of P→Ga coordination compounds

Malbrecht, Brian J.,Dube, Jonathan W.,Willans, Mathew J.,Ragogna, Paul J.

, p. 9644 - 9656 (2015/02/19)

The differing structures and reactivities of "GaI" samples prepared with different reaction times have been investigated in detail. Analysis by FT-Raman spectroscopy, powder X-ray diffraction, 71Ga solid-state NMR spectroscopy, and 127I nuclear quadrupole

Synthesis and characterization of HC{C(Me)N(C6H3-2,6-i-Pr2)}2 MX2 (M = Al, X = Cl, I; M = Ga, In, X = Me, Cl, I): Sterically encumbered β-diketiminate group 13 metal derivatives

Stender,Eichler,Hardman,Power,Prust,Noltemeyer,Roesky

, p. 2794 - 2799 (2008/10/08)

A series of group 13 metal complexes featuring the β-diketiminate ligand [{(C6H3-2,6-i-Pr2)NC(Me)}2CH] - (i.e., [Dipp2nacnac]-, Dipp = C6H3-2,6-i-Pr2) have been prepared and spectroscopically and structurally characterized. The chloride derivatives Dipp2nacnacMCl2 (M = Al (3), Ga (5), In (8)) were isolated in good yield by the reaction of 1 equiv of Dipp2nacnacLi·Et2O (2) and the respective metal halides. The iodide derivatives Dipp2nacnacMl2 (M = Al (4), Ga (6), In (9)), which are useful for reduction to afford M(I) species, were made by a variety of routes. Thus, 4 was obtained by treatment of the previously reported Dipp2nacnacAlMe2 with I2, whereas the gallium analogue 6 was obtained as a product of the reaction of GaI with Dipp2nacnacLi·EtzO, and 9 was obtained by direct reaction of InI3 and the lithium salt. The methyl derivatives Dipp2nacnacMMe2 (M = Ga (7), In (10)), which are analogous to the previously reported Dipp2nacnacAlMe2, were synthesized by the reaction of GaMe3 with Dipp2nacnacH (1) or by reaction of the indium chloride derivative 8 with 2 equiv of MeMgBr in diethyl ether. The compounds 3-10 exist as colorless, air- and moisture-sensitive crystalline solids. Their X-ray crystal structures feature nearly planar C3N2 arrays in the Dipp2nacnac ligand backbone with short C-C and C-N distances that are consistent with a delocalized structure. However, there are large dihedral angles between the C3N2 plane and the N2M metal coordination plane which have been attributed mainly to steric effects. The relatively short M-N distances are consistent with the coordination numbers of the metals and the normal/dative character of the nitrogen ligands. The compounds were also characterized by 1H and 13C NMR spectroscopy. 1H NMR data for 7 revealed equivalent methyl groups whereas the spectrum of 10 displayed two In-Me signals which indicated that ring wagging was slow on the 1H NMR time scale.

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