Boronic acid, 2-triphenylenyl-

Boronic acid, 2-triphenylenyl- - Names and Identifiers

Name	Boronic acid, 2-triphenylenyl-
Synonyms	2-Triphenylene boronic acid Triphenylen-2-ylboronic acid triphenylene-2-ylboronic acid B-2-Triphenylenylboronic acid triphenylene-2-yl boronic acid Boronic acid, 2-triphenylenyl- Boronic acid, B-2-triphenylenyl- 9,10-BenzophenanthreN-2-ylboronicacid
CAS	654664-63-8

Boronic acid, 2-triphenylenyl- - Physico-chemical Properties

Molecular Formula	C18H13BO2
Molar Mass	272.11
Density	1.30
Boling Point	565.5±33.0 °C(Predicted)
pKa	8.53±0.30(Predicted)
Storage Condition	under inert gas (nitrogen or Argon) at 2-8°C

Boronic acid, 2-triphenylenyl- - Introduction

Boronic acid, 2-triphenylenyl-is an organic compound with the chemical formula C24H17BO2. It is a derivative of benzimidazole ligands and has many important properties and applications. The following is a description of its nature, use, preparation and safety information:

Nature:
Boronic acid, 2-triphenylenyl-is a solid with white or light yellow crystal form. It has a relatively high melting and boiling point. This compound is relatively good in solubility and can be dissolved in an organic solvent.

Use:
Boronic acid, 2-triphenylyl-is an important intermediate in organic synthesis. It is often used as a ligand in metal-catalyzed reactions and participates in important catalytic reactions in organic synthesis, such as asymmetric synthesis and cross-coupling reactions. In addition, it can also be used to prepare fluorine intermediates, fluorescent dyes, photosensitive materials, etc.

Preparation Method:
The preparation of Boronic acid, 2-triphenylenyl-is usually achieved by a metal-catalyzed coupling reaction. One common method is the base-catalyzed reaction of a borate ester with an aromatic aldehyde. Preparative processes often require precise control of reaction conditions and purity requirements.

Safety Information:
Boronic acid, 2-triphenylenyl-No significant toxicity or danger has been reported under normal operating conditions. However, as a chemical, it is still necessary to follow laboratory safety procedures. Contact with skin and eyes should be avoided and it should be ensured that the operation is carried out in a well-ventilated environment. During use and storage, care needs to be taken to prevent the risk of fire and explosion and to avoid exceeding the limits of its stability and compatibility. The conditioned scale-up reaction is carried out under the guidance of a professional. If the compound is inhaled or ingested, seek medical attention immediately.

Last Update：2024-04-10 22:29:15