676593-23-0 Usage
Chemical class
Dioxaborinane compounds
It belongs to a class of compounds that contain a boron atom bonded to two oxygen atoms and a five-membered ring.
Structure
Dioxaborinane ring with a phenyl group and two methyl groups
The compound has a dioxaborinane ring structure, which includes a phenyl group with an ethenyl substituent and two methyl groups attached to the boron atom.
Reactivity
Versatile in chemical reactions
Due to its structure, the compound is reactive and can participate in various chemical reactions, making it a useful building block in organic synthesis.
Applications
Organic synthesis, pharmaceuticals, and material science
It is commonly used in the creation of organic compounds and complex molecules, particularly in the fields of pharmaceuticals and material science.
Precursor potential
Development of new materials
The compound has the potential to be used as a precursor in the development of new materials with unique properties and functions.
Molecular weight
Approximately 169.03 g/mol
The molecular weight is an estimate of the mass of one mole of the compound, which can be useful for determining the concentration of a solution or the amount of compound needed for a specific reaction.
Stability
Stable under normal conditions
The compound is generally stable under normal laboratory conditions, making it suitable for use in various chemical reactions and applications.
Solubility
Soluble in organic solvents
It is soluble in common organic solvents, such as dichloromethane, tetrahydrofuran, and dimethyl sulfoxide, which facilitates its use in chemical reactions.
Safety precautions
Handle with care due to potential hazards
As with any chemical compound, it is essential to follow proper safety protocols when handling 1,3,2-Dioxaborinane, 2-(4-ethenylphenyl)-5,5-dimethyl-, including wearing appropriate personal protective equipment and working in a well-ventilated area.
Check Digit Verification of cas no
The CAS Registry Mumber 676593-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,5,9 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 676593-23:
(8*6)+(7*7)+(6*6)+(5*5)+(4*9)+(3*3)+(2*2)+(1*3)=210
210 % 10 = 0
So 676593-23-0 is a valid CAS Registry Number.
676593-23-0Relevant articles and documents
Ruthenium-Catalyzed Carbonylative Coupling of Anilines with Organoboranes by the Cleavage of Neutral Aryl C-N Bond
Xu, Jian-Xing,Zhao, Fengqian,Yuan, Yang,Wu, Xiao-Feng
supporting information, p. 2756 - 2760 (2020/03/30)
Herein, we report the first ruthenium-catalyzed Suzuki-type carbonylative reaction of electronically neutral anilines via C(aryl)-N bond cleavage. Without any ligand and base, diaryl ketones can be obtained in moderate to high yields by using Ru3/su
Selective Monoarylation of Aromatic Ketones and Esters via Cleavage of Aromatic Carbon-Heteroatom Bonds by Trialkylphosphine Ruthenium Catalysts
Kondo, Hikaru,Kochi, Takuya,Kakiuchi, Fumitoshi
supporting information, p. 794 - 797 (2017/03/01)
We report here the ruthenium-catalyzed selective monoarylation of aromatic ketones bearing two ortho carbon-heteroatom (O or N) bonds. Under the newly developed catalyst system consisting of RuHCl(CO)(PiPr3)2, CsF, and sty
Copper(I)-catalyzed carboxylation of aryl- and alkenylboronic esters
Takaya, Jun,Tadami, Satoshi,Ukai, Kazutoshi,Iwasawa, Nobuharu
supporting information; experimental part, p. 2697 - 2700 (2009/05/26)
(Chemical Equation Presented) The copper(I)-catalyzed carboxylation reaction of aryl- and alkenylboronic esters proceeded smoothly under CO 2 to give the corresponding carboxylic acid in good yield. This reaction showed wide generality with higher functional group tolerance compared to the corresponding Rh(I)-catalyzed reaction.
