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Tris-(bromomethylboryl)amine, also known as borabenzene, is a chemical compound with the formula (CH3BBr)3N. It is a colorless, crystalline solid that is soluble in organic solvents. tris-(brommethylboryl)amine is a derivative of borazine, a boron-nitrogen analog of benzene, and is formed by the substitution of three bromine atoms for the hydrogen atoms in the methyl groups of borazine. Tris-(bromomethylboryl)amine is an important reagent in organic synthesis, particularly in the formation of carbon-boron bonds, and is used in the preparation of various organoboron compounds. It is also known for its ability to act as a Lewis acid, facilitating various chemical reactions.

98906-22-0

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98906-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98906-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,9,0 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98906-22:
(7*9)+(6*8)+(5*9)+(4*0)+(3*6)+(2*2)+(1*2)=180
180 % 10 = 0
So 98906-22-0 is a valid CAS Registry Number.

98906-22-0Downstream Products

98906-22-0Relevant academic research and scientific papers

Contributions to the Chemistry of Boron, 155. N-Borylated Borazines

Noeth, Heinrich,Otto, Peter,Storch, Wolfgang

, p. 3020 - 3031 (2007/10/02)

Double stannazane cleavage of (CH3)2B-N2 (1) by CH3BBr2 (1:1) yields 3 (4a).In analogy, N3 (2) reacts with 2 mols of CH3BBr2 and BCl3 to give the N,N',N''-borylated borazines 3 (4b) and3 (4c), respectively.The latter on transhalogenation by BBr3 gives access to 3 (4d). - NMR and IR spectra of 4a-d are in accord with the presence of boryl groups oriented orthogonally or strongly twisted to the borazine ring.Mass spectroscopic fragmentation patterns are characterized by the formation of radicals (CH3, Br) as well as by the elimination of BX3 (or RBX2), borylated iminoboranes, and finally diazadiboretidines.

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