24341-84-2

Basic information

• Product Name: 2-phenyl-1,2-dihydrobenzo[e][1,2]azaborinine
• Synonyms: 2-phenyl-1,2-dihydrobenzo[e][1,2]azaborinine
• CAS NO: 24341-84-2
• Molecular Weight: 205.067
• Mol File: 24341-84-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-phenyl-1,2-dihydrobenzo[e][1,2]azaborinine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-1,2-dihydrobenzo[e][1,2]azaborinine(24341-84-2)
• EPA Substance Registry System: 2-phenyl-1,2-dihydrobenzo[e][1,2]azaborinine(24341-84-2)

Safety Data

• Hazardous Substances Data: 24341-84-2(Hazardous Substances Data)

Upstream product

• 3867-18-3 2-vinylaniline 
• 67114-34-5 2-chloro-1,2-dihydro-1,2-benzaborine 
• 5339-85-5 2-aminophenethyl alcohol 
• 934-56-5 trimethyl(phenyl)stannane 
• 100123-15-7 chloro-phenoxy-phenyl-borane 
• 960-71-4 triphenylborane 
• 591-50-4 iodobenzene 
• 3262-89-3 triphenylboroxine 
• 71-43-2 benzene 
• 100-58-3 phenylmagnesium bromide 
• 2622-55-1 bis(1,2-azabora-2-naphtyl)-oxide 
• 873-51-8 phenylborondichloride 

Downstream Products

• 1105696-59-0 tricarbonyl[(4a,5,6,7,8,8a-η)-1,2-dihydro-2-phenyl-1,2-benzaborine]chromium 
• 1105696-61-4 tricarbonyl[1,2-dihydro-2-(η6-phenyl)-1,2-benzaborine]chromium 
• 1616635-46-1 3-(N-Boc-indol-5-yl)-2-phenyl-2,1-borazaronaphthalene 
• 1616635-45-0 3-(3,5-dimethylisoxazol-4-yl)-2-phenyl-2,1-borazaronaphthalene 
• 1616635-44-9 3-(3-furanyl)-2-phenyl-2,1-borazaronaphthalene 
• 1616635-43-8 2-phenyl-3-(3-thienyl)-2,1-borazaronaphthalene 
• 1616635-42-7 3-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2-phenyl-2,1-borazaronaphthalene 
• 1616635-41-6 3-(3-nitrophenyl)-2-phenyl-2,1-borazaronaphthalene 
• 1616635-40-5 3-(4-fluorophenyl)-2-phenyl-2,1-borazaronaphthalene 
• 1616634-74-2 2,3-diphenyl-2,1-borazaronaphthalene 
• 1616634-99-1 3-bromo-2-phenyl-1,2-dihydrobenzo[e][1,2]azaborinine 

Relevant articles and documents

Rhodium-catalyzed boron arylation of 1,2-azaborines

A Sn-phony in B! BN isosteres of biphenyl compounds are prepared through Rh-catalyzed cross-coupling between 2-chloro-1,2-azaborines and arylstannanes (see scheme). The synthetic method should enable investigations of structure-activity relationships (SAR

Accessing Elaborated 2,1-Borazaronaphthalene Cores Using Photoredox/Nickel Dual-Catalytic Functionalization

A highly effective method for derivatizing 2,1-borazaronaphthalene cores using ammonium alkylbis(catecholato)silicates via photoredox/nickel dual catalysis is reported. By forging Csp3-Csp2 bonds via this approa

Tricarbonylchrommm complexes of 1,2-Dihydro-1,2-benzazaborines

l,2-Dihydro-2-phenyl-1,2-benzazaborine reacts with Cr(CO) 3(CH3CN)3 in THF at 140 °C to form complex 18, in which the phenyl is >n6-bound to chromium. 1,2-Dihydro-2-methyl-1,2-benzazaborine reacts with Cr(CO)su