1133798-41-0

Basic information

• Product Name: 2,4,6-Tris(3,4-dichlorophenyl)boroxin
• Synonyms: 2,4,6-Tris(3,4-dichlorophenyl)boroxin;3,4-Dichlorophenylboronic Anhydride;Tris(3,4-dichlorophenyl)cycloboroxane;Tris(3,4-dichlorophenyl)cycloboroxane 3,4-Dichlorophenylboronic Anhydride
• CAS NO: 1133798-41-0
• Molecular Formula: C₁₈H₉B₃Cl₆O₃
• Molecular Weight: 516
• Product Categories: B (Classes of Boron Compounds);Boronic Acids
• Mol File: 1133798-41-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Solubility: soluble in Methanol
• CAS DataBase Reference: 2,4,6-Tris(3,4-dichlorophenyl)boroxin(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-Tris(3,4-dichlorophenyl)boroxin(1133798-41-0)
• EPA Substance Registry System: 2,4,6-Tris(3,4-dichlorophenyl)boroxin(1133798-41-0)

Safety Data

• Hazardous Substances Data: 1133798-41-0(Hazardous Substances Data)

Usage

General Description

2,4,6-Tris(3,4-dichlorophenyl)boroxin is a chemical compound with the molecular formula C18H9BCl6O3. It is a boronic acid derivative that contains three 3,4-dichlorophenyl groups attached to a boron atom. 2,4,6-Tris(3,4-dichlorophenyl)boroxin is used in organic synthesis as a reagent for the preparation of functionalized molecules. It is also known for its potential application in the development of new drugs and pharmaceuticals. 2,4,6-Tris(3,4-dichlorophenyl)boroxin is a stable and crystalline solid under normal conditions and is considered to be relatively non-toxic. However, its specific properties and potential hazards require careful handling and storage.

Upstream product

• 151169-75-4 3,4-dichlophenylboronic acid 

Downstream Products

• 1133798-33-0 methyl 2-(3,4-dichlorophenyl)-2-p-tolylacetate 
• 55039-68-4 4-(3,4-dichlorophenyl)morpholine 
• 80576-51-8 N,N-dibenzyl-3,4-dichloroaniline 
• 1380035-68-6 C₂₂H₂₀Cl₂O₃S 
• 1358750-87-4 9-[4-(3,4-dichlorophenoxy)phenyl]-3,4,6,7,8,9-hexahydropyrido[2,1-c][1,2,4]thiadiazine 2,2-dioxide 
• 1354729-12-6 C₂₃H₂₀Cl₂O 

Relevant articles and documents

Scalable synthesis of oxazolones from propargylic alcohols through multistep palladium(II) catalysis: β-selective oxidative heck coupling of cyclic sulfonyl enamides and aryl boroxines

A whale of a scale: The title oxidative Heck coupling proceeded with unusual β selectivity to generate a variety of branched substituted oxazolones (see scheme; Ts=p-toluenesulfonyl). The three-step synthesis from readily available starting materials with a simple palladium catalyst and inexpensive reagents could be carried out in a single reaction vessel or scaled up for the preparation of large amounts of these amino acid precursors. Copyright

Arylation and vinylation of α-diazocarbonyl compounds with boroxines

An alternative approach for α-arylation and α-vinylation of carbonyl compounds is described: reaction between aryl-or vinylboroxines with α-diazocarbonyl compounds leads to the formation of α-arylated or α-vinylated carbonyl compounds under mild conditions.