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ChemicalBook--->CAS DataBase List--->866100-14-3

866100-14-3

866100-14-3 Structure

866100-14-3 Structure
IdentificationBack Directory
[Name]

(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid
[CAS]

866100-14-3
[Synonyms]

(9,9-Dimethyl-9H-flu
9,9-diMethyl-9H-fluorene-2,7-diyldiboronic acid
Boronicacid,(9,9-dimethyl-9H-fluorene-2,7-diyl)b
(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid
(9,9-diMethyl-9H-fluoren-2,7-diyl)bisboronic acid
(9,9-dimethyl-9H-fluorene-2,7-diyl)bisboronic acid
(9,9-DIMETHYL-9H-FLUOROENE-2,7-DIYL)BISBORONIC ACID
(9,9-dimethy)-9H-flourene-2,7-diyl)-bisboronic acid
9,9-Dimethyl-9H-fluoren-2,7-diyl-2,7-diboronic acid
BORONIC ACID, (9,9-DIMETHYL-9H-FLUORENE-2,7-DIYL)BIS
BORONIC ACID,B,B'-(9,9-DIMETHYL-9H-FLUORENE-2,7-DIYL)BIS-
BORONIC ACID, (9,9-DIMETHYL-9H-FLUORENE-2,7-DIYL)BIS- (9CI)
(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid ISO 9001:2015 REACH
(9,9-Dimethyl-9H-fluorene-2,7-diyl)diboronic Acid (contains varying amounts of Anhydride)
[EINECS(EC#)]

805-314-9
[Molecular Formula]

C15H16B2O4
[MDL Number]

MFCD08704228
[MOL File]

866100-14-3.mol
[Molecular Weight]

281.91
Chemical PropertiesBack Directory
[storage temp. ]

Store at room temperature
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[HS Code ]

2931900090
Hazard InformationBack Directory
[Chemical Properties]

Off-white powder
[Synthesis]

Triisopropyl borate

5419-55-6

2,7-Dibromo-9,9-dimethylfluorene

28320-32-3

(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid

866100-14-3

The general procedure for the synthesis of 9,9-dimethylfluorene-2,7-diboronic acid from triisopropyl borate and 2,7-dibromo-9,9-dimethylfluorene was as follows: 2,7-dibromo-9,9-dimethylfluorene (14.8 g, 42.4 mmol) was placed in a three-necked flask, 100 mL of tetrahydrofuran (THF) was added, and the reaction was cooled under nitrogen protection to -78 °C and maintained for 30 min. Subsequently, 21 mL of n-butyllithium (2.5 M) solution was added slowly and reacted for 1 hour. Next, triisopropyl borate (14 g) was added and the reaction was continued at low temperature for 1 hour, after which it was gradually warmed to room temperature. After completion of the reaction, the pH was adjusted to 4-5 by adding 2 M hydrochloric acid to the reaction mixture. the aqueous layer was extracted with ethyl acetate, the organic layers were combined and dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give Intermediate A1 (9.5 g, 80% yield).

[References]

[1] Patent: CN106699780, 2017, A. Location in patent: Paragraph 0047; 0048; 0049; 0050
[2] Patent: US8058450, 2011, B2. Location in patent: Page/Page column 43-44
[3] Luminescence, 2015, vol. 30, # 5, p. 549 - 555
Spectrum DetailBack Directory
[Spectrum Detail]

(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid(866100-14-3)1HNMR
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