709022-63-9

Basic information

• Product Name: 9-Anthraceneboronic acid piacol ester
• Synonyms: 9-Anthraceneboronic acid piacol ester;2-(anthracen-9-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;2-(9-Anthryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• CAS NO: 709022-63-9
• Molecular Formula: C₂₀H₂₁BO₂
• Molecular Weight: 304.19054
• Mol File: 709022-63-9.mol
• Article Data: 2

Chemical Properties

• Melting Point: 139.0 to 143.0 °C
• Boiling Point: 465.5±14.0 °C(Predicted)
• Appearance: /
• Density: 1.11±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 9-Anthraceneboronic acid piacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: 9-Anthraceneboronic acid piacol ester(709022-63-9)
• EPA Substance Registry System: 9-Anthraceneboronic acid piacol ester(709022-63-9)

Safety Data

• Hazardous Substances Data: 709022-63-9(Hazardous Substances Data)

Usage

Uses

9-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)anthracene is a reactant in the synthesis of a series of luminescent compounds.

Upstream product

• 1564-64-3 9-Bromoanthracene 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 

Downstream Products

• 1238752-20-9 2,4-bis[3-(9-anthryl)phenyl]-6-phenyl-1,3,5-triazine 
• 1279603-64-3 [5,15-bis(anthracen-9-yl)-10,20-diphenylporphyrinato]nickel(II) 
• 1279603-50-7 [5-(anthracen-9-yl)-10,20-bis(3,5-di-tert-butylphenyl)-15-phenylporphyrinato]nickel(II) 
• 1279603-55-2 [5-(anthracen-9-yl)-15-bromo-10,20-bis(3,5-di-tert-butylphenyl)porphyrinato]nickel(II) 
• 349666-30-4 1-(anthracen-9-yl)-3,5-dibromobenzene 
• 1644567-18-9 C₆₀H₃₈ 
• 1644567-19-0 C₆₀H₃₇Br 
• 102183-23-3 2-(9-anthryl)benzothiazole 
• 41857-56-1 4-(anthracen-9-yl)aniline 
• 1268251-20-2 2-[3,5-di(9-anthryl)phenyl]-4,6-di-p-tolyl-1,3,5-triazine 
• 1268250-83-4 2-[5-(9-anthryl)-4'-(2-pyridyl)biphenyl-3-yl]-4,6-diphenyl-1,3,5-triazine 
• 1380444-38-1 C₃₅H₂₂BrN₃ 
• 1268251-17-7 2-[3,5-di(9-anthryl)phenyl]-4,6-diphenyl-1,3,5-triazine 

Relevant articles and documents

Synthesis and characterization of 6,6″′-bis(anthracen-9-yl)-2, 2′;6′,2″;6″,2″′-quaterpyridine

New bianthracene-quaterpyridine ligand 6,6″′-bis(anthracen-9- yl)-2,2′;6′,2″;6″,2″′-quaterpyridine L has been obtained in a multistep synthesis using Suzuki-Miyaura and Stille-type coupling reactions. The dianthracene ligand L has four nitrogen-donor atoms and can form different supramolecular architectures with transition metal ions. Ligand L and intermediate compounds have been characterized by spectroscopic methods and elemental analyses. 2-(Anthracen-9-yl)-6-bromopyridine and 6-(anthracen-9-yl)-6′-bromo-2,2′-bipyridine have been also characterized by X-ray crystallography.