7297-95-2 Usage
Description
TRIMESITYLBORANE is a chemical compound with the molecular formula (C6H3Me2)3BH, where three mesityl groups are attached to a boron atom, which is connected to a hydrogen atom. It is an organoborane compound known for its unique properties and reactivity, making it a versatile compound in various chemical reactions and applications.
Uses
Used in Chemical Synthesis:
TRIMESITYLBORANE is used as a reactant for the synthesis of sandwich complex derivatives, such as fluoroborate and cyanoborate compounds. These complexes exhibit unique properties and can be utilized in various chemical applications.
Used in Suzuki-Miyaura Coupling:
TRIMESITYLBORANE is used as a reactant in the investigation of the reactivity of aryldimesitylboranes under Suzuki-Miyaura coupling conditions. This coupling reaction is a widely used method in organic chemistry for the formation of carbon-carbon bonds, particularly in the synthesis of biaryl compounds.
Used in Mass Spectrometry:
TRIMESITYLBORANE is employed in laser desorption ionization mass spectrometry investigations. This technique is used to analyze the molecular structure and composition of various compounds, including TRIMESITYLBORANE and its derivatives.
Used in Ion Conductive Materials:
TRIMESITYLBORANE is used in the study of ion conductive characteristics of boron-stabilized carbanions. These studies contribute to the development of new materials with improved ion conductivity, which can be applied in various industries, such as energy storage and electronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 7297-95-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7297-95:
(6*7)+(5*2)+(4*9)+(3*7)+(2*9)+(1*5)=132
132 % 10 = 2
So 7297-95-2 is a valid CAS Registry Number.
InChI:InChI=1/C27H33B/c1-16-10-19(4)25(20(5)11-16)28(26-21(6)12-17(2)13-22(26)7)27-23(8)14-18(3)15-24(27)9/h10-15H,1-9H3
7297-95-2Relevant articles and documents
Lewis Acidic Boranes, Lewis Bases, and Equilibrium Constants: A Reliable Scaffold for a Quantitative Lewis Acidity/Basicity Scale
Mayer, Robert J.,Hampel, Nathalie,Ofial, Armin R.
supporting information, p. 4070 - 4080 (2021/01/29)
A quantitative Lewis acidity/basicity scale toward boron-centered Lewis acids has been developed based on a set of 90 experimental equilibrium constants for the reactions of triarylboranes with various O-, N-, S-, and P-centered Lewis bases in dichloromethane at 20 °C. Analysis with the linear free energy relationship log KB=LAB+LBB allows equilibrium constants, KB, to be calculated for any type of borane/Lewis base combination through the sum of two descriptors, one for Lewis acidity (LAB) and one for Lewis basicity (LBB). The resulting Lewis acidity/basicity scale is independent of fixed reference acids/bases and valid for various types of trivalent boron-centered Lewis acids. It is demonstrated that the newly developed Lewis acidity/basicity scale is easily extendable through linear relationships with quantum-chemically calculated or common physical–organic descriptors and known thermodynamic data (ΔH (Formula presented.)). Furthermore, this experimental platform can be utilized for the rational development of borane-catalyzed reactions.
Derivative of tetra-substituted pyrrolo [3,2-b] pyrrole and organic electroluminescence device based on same
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Paragraph 0049; 0050, (2017/05/18)
The invention provides a derivative of 2,5-substituted 1,4-di(4-tert-butyl-phenyl) pyrrolo [3,2-b] pyrrole, and application of the derivative. The derivative has the following structural formula as shown in the specification; in the formula, R represents
