1078145-13-7

Basic information

• Product Name: (CH₃C₅H₄N)2BC₄(C₆H₅)4⁽¹⁺⁾*B(C₆H₃(CF₃)2)4^(1-)=[(CH₃C₅H₄N)2BC₄(C₆H₅)4][B(C₆H₃(CF₃)2)4]
• Synonyms: (CH₃C₅H₄N)2BC₄(C₆H₅)4⁽¹⁺⁾*B(C₆H₃(CF₃)2)4^(1-)=[(CH₃C₅H₄N)2BC₄(C₆H₅)4][B(C₆H₃(CF₃)2)4]
• CAS NO: 1078145-13-7
• Molecular Weight: 1416.75
• Mol File: 1078145-13-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (CH₃C₅H₄N)2BC₄(C₆H₅)4⁽¹⁺⁾*B(C₆H₃(CF₃)2)4^(1-)=[(CH₃C₅H₄N)2BC₄(C₆H₅)4][B(C₆H₃(CF₃)2)4](CAS DataBase Reference)
• NIST Chemistry Reference: (CH₃C₅H₄N)2BC₄(C₆H₅)4⁽¹⁺⁾*B(C₆H₃(CF₃)2)4^(1-)=[(CH₃C₅H₄N)2BC₄(C₆H₅)4][B(C₆H₃(CF₃)2)4](1078145-13-7)
• EPA Substance Registry System: (CH₃C₅H₄N)2BC₄(C₆H₅)4⁽¹⁺⁾*B(C₆H₃(CF₃)2)4^(1-)=[(CH₃C₅H₄N)2BC₄(C₆H₅)4][B(C₆H₃(CF₃)2)4](1078145-13-7)

Safety Data

• Hazardous Substances Data: 1078145-13-7(Hazardous Substances Data)

Upstream product

• 108-89-4 picoline 
• 79060-88-1 sodium tetrakis[(3,5-di-trifluoromethyl)phenyl]borate 
• 62707-11-3 1-chloro-2,3,4,5-tetraphenylborole 
• 1078145-08-0 (CH₃C₅H₄N)ClBC₄(C₆H₅)4 

Relevant articles and documents

Direct functionalization at the boron center of antiaromatic chloroborole

The presence of a reactive B-Cl bond allowed for the direct functionalization of the boron center in antiaromatic chloroborole ClBC 4Ph4, thus allowing for a selective fine tuning of the optical properties of borole derivatives and facilitating a potential new approach toward the introduction of borole moieties into the backbone of organic π-conjugated frameworks. The Royal Society of Chemistry.