58347-22-1

Basic information

• Product Name: 2-(phenylethynyl)benzo[d][1,3,2]dioxaborole
• Synonyms: 2-(phenylethynyl)benzo[d][1,3,2]dioxaborole
• CAS NO: 58347-22-1
• Molecular Weight: 220.035
• Mol File: 58347-22-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(phenylethynyl)benzo[d][1,3,2]dioxaborole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(phenylethynyl)benzo[d][1,3,2]dioxaborole(58347-22-1)
• EPA Substance Registry System: 2-(phenylethynyl)benzo[d][1,3,2]dioxaborole(58347-22-1)

Safety Data

• Hazardous Substances Data: 58347-22-1(Hazardous Substances Data)

Upstream product

• 1086138-68-2 C₁₀H₇BO₃ 
• 536-74-3 phenylacetylene 
• 55718-76-8 2-chloro-1,3,2-benzodioxaborole 
• 1199-95-7 1-(trimethylstannyl)-2-phenylethyne 

Downstream Products

• 809277-80-3 3-(1,3,2-benzodioxaborolyl)-4-phenyl-1,2-bis(tricarbonylcobalta)tetrahedrane 
• 885333-59-5 closo-1-phenylethynyl-2,3-diethyl-2,3-dicarbaheptaborane⁽⁷⁾ 

Relevant articles and documents

Boron Recycling in the Metal-Free Transfer C-H Borylation of Terminal Alkynes and Heteroarenes

Transfer C-H borylation is an isodesmic approach to the borylation reaction using B-C-containing molecules as boron sources. In this work, we report that 2-mercaptothiazole and other analogues are active for the metal-free borylation of heterocycles and t

Cobalt-mediated cyclooligomerization reactions of borylacetylenes

Reaction of bis(diethylamino) acetylene (1) with lithium and chlorobis(dimethylamino)borane yields 1-[bis(dimethylamino)boryl]-2- (diethylamino)acetylene (2). Treatment of 1-aryl-2-(trimethylstannyl)acetylenes 3 with chlorobis(diisopropylamino)borane results in the quantitative formation of 1-aryl-2-[bis(diisopropylamino)boryl]acetylene compounds 4. The 1-aryl-2-borylacetylene derivatives 5, 6, and 7 are obtained by the reaction of 3 with the appropriate haloborane, or by reacting 4 with two equivalents of HCl and one equivalent of catechol, dithiocatechol and 2-hydroxythiophenol. The catalytic cyclotrimerizations of 5a-d with [CpCo(CO)2] or [Co 2(CO)8] lead to isomeric mixtures of the triborylbenzene derivatives 8a-d and 8a′-d′, whereas 6a-d and 7a-b undergo cyclotrimerization only with catalytic amount of [Co2(CO) 8], to give isomeric mixtures of the triborylbenzene derivatives 12a-d/12a′-d′ and 13a-b/13a′-b′, respectively. The reaction of 2 with a stoichiometric amount of (η5- cyclopentadienyl)bis(ethene)cobalt leads to (η5-cyclopentadienyl) (η4-cyclobutadiene)cobalt complexes 9. The analogous complexes 10 and 11 are obtained by the reactions of 6 and 7 with a stoichiometric amount of (η5-cyclopentadienyl)dicarbonylcobalt. Treatment of Co 2(CO)8 with 5a, 6a, and 7a yields the dicobaltatetrahedranes 14a, 15a and 16a. Compound 15a reacts with two equivalents of diphenylacetylene and 1-(1,3,2-benzodioxaborolyl)-2- phenylacetylene (5a), to furnish (1,3,2-benzodithiaborolyl)pentaphenylbenzene (17) and bis(1,3,2-benzodioxaborolyl)(1,3,2-benzodithiaborolyl)triphenylbenzene (18), respectively. The new compounds have been characterized by NMR spectroscopy and mass spectrometry, as well as by X-ray structural analyses for 4a, 5a, 6a, and 10a. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.