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Tris(4-iodophenyl)boroxine is a complex organic compound with the chemical formula C18H12BINO3. It is a derivative of boroxine, which is a boron-containing heterocyclic compound. The molecule consists of a boron atom at the center, bonded to three 4-iodophenyl groups, which are phenyl rings with an iodine atom attached at the para position. tris(4-iodo phenyl)boroxine is known for its unique electronic properties and potential applications in materials science, particularly in the development of organic semiconductors and as a precursor in the synthesis of other complex molecules. Due to the presence of the heavy iodine atoms, it may also be of interest in studies involving halogen bonding or as a component in heavy atom effects.

7519-90-6

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7519-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7519-90-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7519-90:
(6*7)+(5*5)+(4*1)+(3*9)+(2*9)+(1*0)=116
116 % 10 = 6
So 7519-90-6 is a valid CAS Registry Number.

7519-90-6Downstream Products

7519-90-6Relevant academic research and scientific papers

Polymorphism in Fe[(p-IC6H4)B(3-Mepz) 3]2 (pz = Pyrazolyl): Impact of supramolecular structure on an Iron(ll) electronic Spin-state crossover

Reger, Daniel L.,Gardinier, James R.,Smith, Mark D.,Shahin, Ahmed M.,Long, Gary J.,Rebbouh, Leila,Grandjean, Fernande

, p. 1852 - 1866 (2005)

The new ligands Na[(p-IC6H4)B(3-Rpz)3] (R = H, Me) have been prepared by converting I2C6H 4 to IC6H4SiMe3 with Li +Bu and SiMe3Cl, and then to IC6H 4BBr2 with BBr3 and subsequent reaction with 3 equiv of (un)substituted pyrazole and 1 equiv of NaO+Bu. These new ligands react with FeBr2 to give either purple, low-spin Fe[(p-IC6H4)B(pz)3]2 or colorless, high-spin Fe[(p-IC6H4)B(3-Mepz)3]2. Depending upon the crystallization conditions, Fe[(p-IC6H 4)B(3-Mepz)3]2 can exist both as two polymorphs and as a methylene chloride solvate. An examination of these polymorphs by variable-temperature X-ray crystallography, magnetic susceptibility, and Moessbauer spectroscopy has revealed different electronic spin-state crossover properties for each polymorph and yields insight into the influence of crystal packing, independent of other electronic perturbations, on the spin-state crossover. The first polymorph of Fe[(p-IC6H 4)B(3-Mepz)3]2 has a highly organized three-dimensional supramolecular structure and does not undergo a spin-state crossover upon cooling to 4 K. The second polymorph of Fe[(p-IC 6H4)B(3-Mepz)3]2 has a stacked two-dimensional supramolecular structure, a structure that is clearly less well organized than that of the first polymorph, and undergoes an abrupt iron(II) spin-state crossover from high spin to low spin upon cooling below ca. 130 K. The crystal structure of the methylene chloride solvate of Fe[(p-IC 6H4)B(3-Mepz)3]2 has a similar stacked two-dimensional supramolecular structure, but the crystals readily lose the solvate. The resulting desolvate undergoes a gradual spin-state crossover to the low-spin state upon cooling below ca. 235 K. It is clear from a comparison of the structures that the longrange solid-state organization of the molecules, which is controlled by noncovalent supramolecular interactions, has a strong impact upon the spin-state crossover, with the more highly organized structures having lower spincrossover temperatures and more abrupt spin-crossover behavior.

A process for preparing carboxyl boric acid

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Paragraph 0035; 0036, (2017/08/25)

The invention discloses a method for preparing carboxyl phenylboronic acid. The method comprises the following steps of starting from halogenated phenylboronic acid, heating, refluxing and dehydrating in a solvent to form a tripolymer; then forming a grignard reagent of corresponding tripolymer from tripolymer and magnesium metal or isopropyl magnesium chloride; then introducing a carbon dioxide gas at low temperature or adding dry ice for reaction; after the reaction is finished, adding hydrochloric acid, regulating till pH is equal to 2-3, and hydrolyzing; and precipitating carboxyl phenylboronic acid, filtering, and drying to obtain a pure product. The method disclosed by the invention can achieve good yield on ortho-position, meta-position and para-position carboxyl phenylboronic acid, is simple in used reagent and easy and convenient to operate and prevents the generation of a large quantity of solid wastes.

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