7147-07-1

Basic information

• Product Name: 2-(dibenzo[b,e]borinin-5(10H)-yloxy)ethanamine
• CAS NO: 7147-07-1
• Molecular Formula: C₁₅H₁₆BNO
• Molecular Weight: 237.1046
• Mol File: 7147-07-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 359.4°C at 760 mmHg
• Flash Point: 171.2°C
• Density: 1.11g/cm³
• Vapor Pressure: 2.38E-05mmHg at 25°C
• Refractive Index: 1.596
• CAS DataBase Reference: 2-(dibenzo[b,e]borinin-5(10H)-yloxy)ethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(dibenzo[b,e]borinin-5(10H)-yloxy)ethanamine(7147-07-1)
• EPA Substance Registry System: 2-(dibenzo[b,e]borinin-5(10H)-yloxy)ethanamine(7147-07-1)

Safety Data

• Hazardous Substances Data: 7147-07-1(Hazardous Substances Data)

Usage

General Description

2-(dibenzo[b,e]borinin-5(10H)-yloxy)ethanamine is a chemical compound with a complex molecular structure. It consists of a central boron atom bonded to two benzene rings, as well as an ethanamine group. 2-(dibenzo[b,e]borinin-5(10H)-yloxy)ethanamine belongs to the class of boron-containing chemicals and is often used in pharmaceutical and chemical research. It can be synthesized through a series of chemical reactions involving boron-containing compounds and ethanamine derivatives. The exact properties and uses of 2-(dibenzo[b,e]borinin-5(10H)-yloxy)ethanamine have not been widely documented, but it likely has potential applications in various fields such as medicine, materials science, and organic chemistry. However, further research and testing are necessary to fully understand its properties and potential uses.

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Relevant articles and documents

Methylene Bridging Effect on the Structures, Lewis Acidities and Optical Properties of Semi-planar Triarylboranes

Three synthetic methods towards semi-planar triarylboranes with two aryl rings connected by a methylene bridge have been developed. The fine-tuning of their stereoelectronic properties and Lewis acidities was achieved by introducing fluorine, methyl, methoxy, n-butyl and phenyl groups either at their exocyclic or bridged aryl rings. X-ray diffraction analysis and quantum-chemical calculations provided quantitative information on the structural distortion experienced by the near planar hydro-boraanthracene skeleton during the association with Lewis bases such as NH3 and F?. Though the methylene bridge between the ortho-positions of two aryl rings of triarylboranes decreased the Gibbs free energies of complexation with small Lewis bases by less than 5 kJ mol?1 relative to the classical Lewis acid BAr3, the steric shielding of the CH2 bridge is sufficient to avoid the formation of Lewis adducts with larger Lewis bases such as triarylphosphines. A newly synthesized spirocyclic amino-borane with a long intramolecular B?N bond that could be dissociated under thermal process, UV-irradiation, or acidic conditions might be a potential candidate in Lewis pairs catalysis.