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203927-98-4

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203927-98-4 Usage

Description

9,9-Dihexyfluorene-2,7-diboronic acid is an organic compound that features a fluorene core with two boronic acid groups attached at the 2 and 7 positions. This molecule is known for its unique chemical properties and potential applications in various fields due to its ability to form stable covalent bonds with other molecules.

Uses

Used in Chemical Synthesis:
9,9-Dihexyfluorene-2,7-diboronic acid is used as a reactant for Rhodium-catalyzed hydroarylation, a chemical reaction that involves the addition of an aromatic ring to an unsaturated compound, facilitated by a rhodium catalyst.
Used in Nanotechnology:
In the field of nanotechnology, 9,9-dihexyfluorene-2,7-diboronic acid is used for molecular bridging of silicon nanogaps. This application takes advantage of the compound's ability to form strong bonds, allowing for the creation of stable connections between nanoscale structures.
Used in Polymer Science:
9,9-Dihexyfluorene-2,7-diboronic acid is utilized in the preparation of boronate ester coordinated polymer and macrocycle for sensing and storing of benzene. The compound's chemical properties make it suitable for creating materials with specific sensing capabilities, which can be useful in various industrial applications.
Used in Material Science:
In material science, 9,9-dihexyfluorene-2,7-diboronic acid is employed in the synthesis of light-emitting carbazole-based copolymers bearing cyano-substituted arylenevinylene chromophore. These copolymers have potential applications in the development of advanced optoelectronic devices, such as organic light-emitting diodes (OLEDs).
Used in Pharmaceutical Industry:
9,9-Dihexyfluorene-2,7-diboronic acid is used as a reactant for Rhodium-catalyzed arylation, a chemical process that can lead to the synthesis of various pharmaceutical compounds with potential therapeutic applications. The versatility of this compound in chemical reactions makes it a valuable tool in the development of new drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 203927-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,9,2 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 203927-98:
(8*2)+(7*0)+(6*3)+(5*9)+(4*2)+(3*7)+(2*9)+(1*8)=134
134 % 10 = 4
So 203927-98-4 is a valid CAS Registry Number.
InChI:InChI=1/C25H36B2O4/c1-3-5-7-9-15-25(16-10-8-6-4-2)23-17-19(26(28)29)11-13-21(23)22-14-12-20(27(30)31)18-24(22)25/h11-14,17-18,28-31H,3-10,15-16H2,1-2H3

203927-98-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H55817)  9,9-Di-n-hexylfluorene-2,7-diboronic acid, 97%   

  • 203927-98-4

  • 250mg

  • 1852.0CNY

  • Detail
  • Alfa Aesar

  • (H55817)  9,9-Di-n-hexylfluorene-2,7-diboronic acid, 97%   

  • 203927-98-4

  • 1g

  • 5758.0CNY

  • Detail

203927-98-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (7-borono-9,9-dihexylfluoren-2-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 9,9-dihexylfluoren-2,7-yldiboronic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:203927-98-4 SDS

203927-98-4Relevant articles and documents

Synthesis and nearly monochromatic photoluminescence properties of conjugated copolymers containing fluorene and rare earth complexes

Ling,Kang,Neoh,Huang, Wei

, p. 6995 - 7003 (2003)

A series of novel conjugated copolymers containing 9,9-dihexylfluorene and europium complex-chelated benzoate units in the main chain had been synthesized through a three-step process, involving Suzuki coupling copolymerization, hydrolysis of benzoate units, and postchelation. The chemical structures of the copolymers were characterized by FT-IR, 1H NMR, 13C NMR, GPC, and ToF-SIMS. The copolymers exhibited relatively high glass transition temperatures after incorporation of the rare earth complexes. The photoluminescence (PL) properties of the copolymer complexes in solution and in film form were investigated. Intramolecular energy transfer from the fluorene groups to the europium complex occurred in diluted solutions of the copolymer. The efficiency of this process depended strongly on the structure of the ligands for the europium complex and the composition of the copolymers. The PL spectra of the copolymer complexes consisted of two emission bands, one in the 350-550 nm region and another at around 612 nm, corresponding to the π* → π transitions of the fluorene moieties and the f-f transitions of the europium ions, respectively. In the copolymer films cast from solutions, emission from the fluorene groups could be suppressed, and the absorbed excitation energy was transferred effectively to the europium complexes in the copolymer. Nearly monochromatic red emission (with a line width of about 4 nm) was detected under UV excitation at room temperature.

New pyrimidine- and fluorene-containing oligo(arylene)s: Synthesis, crystal structures, optoelectronic properties and a theoretical study

Hughes, Gregory,Wang, Changsheng,Batsanov, Andrei S.,Fern, Michael,Frank, Stephen,Bryce, Martin R.,Perepichka, Igor F.,Monkman, Andrew P.,Lyons, Benjamin P.

, p. 3069 - 3077 (2003)

New pyrimidine containing oligo(arylene)s, notably the pyrimidine-fluorene hybrid systems 13-16, have been synthesised by Suzuki cross-coupling methodology. An efficient synthesis of the key reagent 9,9-dihexylfluorene-2,7-diboronic acid 10 from 2,7-dibro

Synthesis and Two-Photon Properties of Multi-Branched Fluorophores Composed of Ladder-Type Conjugated Cores and Functionalized Diquinoxalinylamino Peripheries

Lin, Tzu-Chau,Li, Mei-Ling,Liu, Che-Yu,Tsai, Ming-Yu,Lee, Ying-Hsuan,Febriani, Yuyun,Lin, Ja-Hon,Shen, Yu-Kai

, p. 1615 - 1621 (2015/10/05)

Two multipolar fluorophores using ladder-type oligo-(p-phenylene) units as the central π-bridges and functionalized diquinoxalinylamino moieties as the peripheral groups have been synthesized and experimentally shown to manifest strong two-photon absorpti

Multi-Functional Copolymers Comprising Rare Earth Metal Complexes and Devices Thereof

-

, (2008/06/13)

The invention relates to copolymer complexes of the formula (I): wherein [Ax-[B(C)]y-Dz] denotes a single unit of the copolymer complex that is repeated n times, wherein n is an integer greater than one, and wherein the single unit comprises a conjugated backbone coordinated to a complex (C) comprising rare earth metal(s); x, y and z are numbers greater than zero such that x=y+z; A is independently selected from a group consisting of: fluorene, carbazole, oxadiazole, triphenylamine or derivatives thereof; B is a functional ligand selected from the group consisting of: benzoic acid, 1,3-diphenylpropane-1,3-dione, 1,10-phenanthroline, 2,2-bipyridine, or derivatives thereof; and D is independently selected from a group consisting of: fluorene, carbazole, oxadiazole, triphenylamine or derivatives thereof.

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