2,4,6-Tris(3,4,5-trifluorophenyl)boroxin

2,4,6-Tris(3,4,5-trifluorophenyl)boroxin - Names and Identifiers

Name	2,4,6-Tris(3,4,5-trifluorophenyl)boroxin
Synonyms	Tris(3,4,5-trifluorophenyl)boroxin 3,4,5-TRIFLUOROPHENYLBORONIC ANHYDRIDE 2,4,6-Tris(3,4,5-trifluorophenyl)boroxin TRIS(3,4,5-TRIFLUOROPHENYL)CYCLOBOROXANE 2,4,6-TRIS(3,4,5-TRIFLUOROPHENYL)BOROXIN Boroxin,tris(3,4,5-trifluorophenyl)- (9CI) Boroxin, 2,4,6-tris(3,4,5-trifluorophenyl)- 2,4,6-Tris(3,4,5-trifluorophenyl)-1,3,5,2,4,6-trioxatriborinane 3,4,5-Trifluorophenylboronic Anhydride Tris(3,4,5-trifluorophenyl)cycloboroxane
CAS	223440-94-6

2,4,6-Tris(3,4,5-trifluorophenyl)boroxin - Physico-chemical Properties

Molecular Formula	C18H6B3F9O3
Molar Mass	473.66
Density	1.49±0.1 g/cm3(Predicted)
Boling Point	375.9±52.0 °C(Predicted)
Storage Condition	Room Temprature
MDL	MFCD03844809

2,4,6-Tris(3,4,5-trifluorophenyl)boroxin - Introduction

2,4,6-Tris(3,4,5-trifluorophenyl)boroxin is an organic compound with the chemical formula C18H6BF9O. It is a solid with a white to yellowish color. The following is a description of some properties, uses, preparation and safety information about this compound:

Nature:
1. Appearance: 2,4,6-Tris(3,4,5-trifluorophenyl) is boroxin a solid, white to yellowish.
2. Melting point: Its melting point is usually in the range of 170-175°C.
3. Solubility: It can be dissolved in some organic solvents, such as dichloromethane, dimethyl sulfoxide and acetonitrile.

Use:
2,4,6-Tris(3,4,5-trifluorophenyl)boroxin has some important applications in organic synthesis:
1. Catalyst: It is an effective catalyst and can be used in various organic reactions, such as oxygen hybridization reactions, aromatic olefin ring insertion reactions, etc.
2. Ligand: It can form complexes with metals and is widely used in catalysts and drugs.

Preparation Method:
The synthesis of 2,4,6-Tris(3,4,5-trifluorophenyl)boroxin is usually carried out by the following steps:
1. Add phenylboronic acid and trifluorophenol to the reaction vessel.
2. Add a catalyst, usually an alkali metal to the blow of benzene boric acid or sodium hydroxide.
3. The reaction vessel is heated to produce a dehydration reaction of boron oxide.
4. After filtration and crystallization, 2,4,6-Tris(3,4,5-trifluorophenyl)boroxin was obtained.

Safety Information:
For the safety information of 2,4,6-Tris(3,4,5-trifluorophenyl)boroxin, due to insufficient relevant studies, specific data on its toxicity and safety are not clear. However, in general, appropriate protective measures such as gloves, goggles and laboratory suits should be taken when handling chemicals. Avoid contact with skin and eyes, avoid inhalation or ingestion. At the same time, when conducting chemical experiments, the laboratory safety operation procedures should be strictly observed.

Last Update：2024-04-09 21:11:58