89566-59-6

Basic information

• Product Name: Borinic acid, bis(4-chlorophenyl)-
• CAS NO: 89566-59-6
• Molecular Formula: C12H9BCl2O
• Molecular Weight: 250.92
• Mol File: 89566-59-6.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Borinic acid, bis(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Borinic acid, bis(4-chlorophenyl)-(89566-59-6)
• EPA Substance Registry System: Borinic acid, bis(4-chlorophenyl)-(89566-59-6)

Safety Data

• Hazardous Substances Data: 89566-59-6(Hazardous Substances Data)

Upstream product

• 873-77-8 (4-chlorphenyl)magnesium bromide 
• 13195-76-1 triisobutyl borate 
• 637-87-6 1-Chloro-4-iodobenzene 
• 18494-92-3 (diethylamino)borane 
• 7732-18-5 water 
• 61733-90-2 B-(2-aminoethoxy)bis(4-chlorophenyl)borane 
• 106-39-8 bromochlorobenzene 
• 102-24-9 cyclotriboric acid trimethyl ester 
• 121-43-7 Trimethyl borate 

Downstream Products

• 188425-85-6 boscalid 
• 1204-44-0 2-(4-chlorophenyl)aniline 
• 19482-11-2 4-chloro-4'-methylbiphenyl 
• 7012-37-5 2,4,4'-Trichlorobiphenyl 
• 2050-68-2 4,4'-dichlorobiphenyl 
• 23055-77-8 4'-chloro-4-bromo-biphenyl 
• 5002-07-3 4'-(4-chlorophenyl)acetophenone 
• 30894-93-0 2-chloro-4-(4-chlorophenyl)-6-phenyl-1,3,5-triazine 
• 10202-46-7 2,4-dichloro-6-(4-chlorophenyl)-[1,3,5]triazine 
• 276671-67-1 [(CH₃)Co((ONC(CH₃)C(CH₃)NOB(C₆H₄Cl)2)2)(H₂O)] 
• 276671-65-9 [(H₃C)Co((ONC(CH₃)C(CH₃)NOB(C₆H₄Cl)2)2)(C₅H₅N)] 
• 276671-81-9 [(C₆H₅)Co((ONC(CH₃)C(CH₃)NOB(C₆H₄Cl)2)2)(C₃H₃N₂CH₃)] 
• 276671-79-5 [(H₃C)Co((ONC(CH₃)C(CH₃)NOB(C₆H₄Cl)2)2)(C₃H₃N₂CH₃)] 
• 872044-92-3 bis(4-chlorophenyl)borinic acid 4-(hydroxymethyl)imidazole ester 

Relevant articles and documents

Palladium-catalyzed B-diarylation of diethylaminoborane for the synthesis of diarylborinic acids

The palladium-catalyzed synthesis of diarylborinic acid derivatives by intermolecular cross-coupling between aryl iodides and (amino)dihydrideborane is reported. The key to success of the reaction is the use of a less bulky diethylaminoborane reagent, which facilitates the second B-arylation.

Borinic acid catalysed peptide synthesis

The catalytic synthesis of peptides is a major challenge in the modern organic chemistry hindered by the well-established use of stoichiometric coupling reagents. Herein, we describe for the first time that borinic acid is able to catalyse this reaction under mild conditions with an improved activity compared to our recently developed thiophene-based boronic acid. This catalyst is particularly efficient for peptide bond synthesis affording dipeptides in good yields without detectable racemization.

Anti-viral uses of borinic acid complexes

Compositions and methods of use of borinic acid complexes, especially hydroxyquinoline, imidazole and picolinic acid derivatives, as anti-viral agents as well as therapeutic agents for the treatment of diseases caused by viruses are described.