Identification | Back Directory | [Name]
1,3,5-Phenyltriboronic acid, pinacol ester | [CAS]
365564-05-2 | [Synonyms]
5-Phenyltriboronic acid 1,3,5-Benzenetriboronic Acid Tris(pinacoL 1,3,5-Phenyltriboronic acid, pinacol ester 1,3,5-Phenyltriboronic acid, tris(pinacol) ester 1,3,5-Benzenetriboronic Acid Tris(pinacol) Ester benzene-1,3,5-triyltriboronic acid pinacol ester 2-[3,5-Bis(tetramethyl-1,3,2-dioxaborolan-2-yl)phen 1,3,5-Phenyltriboronic acid, tris(pinacol) ester >=97% 1,3,5-Phenyltriboronicacid,Tris(Pinacol)Esteraldrichcpr 1,3,5-Tris(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzene OC1418, 1,3,5-Tris(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene 2,2',2''-(1,3,5-Benzenetriyl)tris(4,4,5,5-tetramethyl-1,3,2-dioxaborolane) 1,3,2-Dioxaborolane, 2,2',2''-(1,3,5-benzenetriyl)tris[4,4,5,5-tetramethyl- 2-[3,5-Bis(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | [Molecular Formula]
C24H39B3O6 | [MDL Number]
MFCD17167305 | [MOL File]
365564-05-2.mol | [Molecular Weight]
309.724 |
Chemical Properties | Back Directory | [Melting point ]
286-287°C | [Boiling point ]
555.6±45.0 °C(Predicted) | [density ]
1.05±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
powder or crystals |
Hazard Information | Back Directory | [Uses]
1. Fabricated a 2D COF which when deposited onto a Gold electrode increases the hydrogen evolution reaction(HER) activity by up to three times compared with bare Gold. 2. Used as an aromatic linker to synthesise a twisted Perylenediimide (PDI) base multimer that has potential applications in organic photovoltaics. |
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