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2,2'-(9,9-Didecyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a complex organic chemical compound characterized by its long molecular structure. It features fluorene and tetramethyl-1,3,2-dioxaborolane moieties, which are aromatic organic compounds. The incorporation of boron in the dioxaborolane groups endows the compound with unique chemical properties, such as the capability to engage in Suzuki coupling reactions. The extended didecyl chains attached to the fluorene group render 2,2'-(9,9-Didecyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl-1,3,2-dioxaborolane suitable for applications as a polymeric material or in organic electronic devices. This chemical may have potential uses in various fields, including organic synthesis, materials science, and electronics.

711026-06-1

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  • 2-[9,9-didecyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)fluoren-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

    Cas No: 711026-06-1

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    Cas No: 711026-06-1

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711026-06-1 Usage

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Used in Organic Synthesis:
2,2'-(9,9-Didecyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure and reactivity make it a valuable building block in the synthesis of complex organic molecules.
Used in Materials Science:
In the field of materials science, 2,2'-(9,9-Didecyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a component in the development of polymeric materials. The presence of long didecyl chains and aromatic moieties contributes to the compound's potential for creating materials with specific properties, such as improved thermal stability or enhanced mechanical strength.
Used in Electronics:
2,2'-(9,9-Didecyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a material in the fabrication of organic electronic devices. Its electronic properties, such as charge transport and light-emitting capabilities, make it a promising candidate for applications in organic light-emitting diodes (OLEDs), organic solar cells, and other electronic components.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, the unique chemical properties and structural features of 2,2'-(9,9-Didecyl-9H-fluorene-2,7-diyl)bis[4,4,5,5-tetramethyl-1,3,2-dioxaborolane may also find applications in the pharmaceutical industry. It could potentially be used as a starting material for the synthesis of novel pharmaceutical compounds or as a component in drug delivery systems, leveraging its ability to participate in Suzuki coupling reactions for the creation of diverse molecular structures with potential therapeutic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 711026-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,1,0,2 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 711026-06:
(8*7)+(7*1)+(6*1)+(5*0)+(4*2)+(3*6)+(2*0)+(1*6)=101
101 % 10 = 1
So 711026-06-1 is a valid CAS Registry Number.

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  • TCI America

  • (B4588)  2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9-didecylfluorene  >98.0%(HPLC)

  • 711026-06-1

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  • 2,390.00CNY

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711026-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[9,9-didecyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)fluoren-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 9,9-Didecylfluorene-2,7-diboronic Acid Bis(pinacol) Ester

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:711026-06-1 SDS

711026-06-1Downstream Products

711026-06-1Relevant articles and documents

An all-small-molecule organic solar cell derived from naphthalimide for solution-processed high-efficiency nonfullerene acceptors

Yadagiri,Narayanaswamy,Revoju, Srikanth,Eliasson, Bertil,Sharma, Ganesh D.,Singh, Surya Prakash

supporting information, p. 709 - 717 (2019/01/24)

Two small molecules BYG-1 and BYG-2 with fluorene donor and benzothiadiazole acceptor units connected to the terminal naphthamide group via ethyne linker were designed and synthesized. In this work we have discussed the effect of fluorine atoms connected with electron withdrawing benzothiadiazole unit to the fluorene core (BYG-1). In this study, we have fabricated solar cells with small-molecular donor and acceptor materials in the device architecture of bulk-heterojunction, using highly conjugated BYG-1 and BYG-2 as electron acceptors along with an appropriate small molecule donor (SMD). After improving the device architecture of the active layer using a suitable donor-to-acceptor weight ratio with solvent vapour annealing, we achieved power conversion efficiencies of 8.67% and 7.12% for BYG-1 and BYG-2, respectively. The superior photovoltaic performance of the fluorine-substituted BYG-1 can be attributed to its higher crystallinity, more balanced charge transport mobilities and efficient exciton dissociation.

Synthesis and characterization of violet light emitting polymer based on fluorene and dimethylsilane

Bae, Dong-Soo,Lee, Dong-Hyun,Eim, Don-Eon,Hu, Seung-Eun,Jung, Shihaw,Kim, Ran,Hwang, Jaeyoung,Kim, Yun-Hi

, p. 26 - 32 (2013/10/01)

New fluorene based light emitting polymer, poly[(4-(9,9-didecyl-9H-fluoren- 2-yl) phenyl)dimethyl(phenyl)silane] (PFDPS), was synthesized by palladium-catalzed Suzuki coupling reaction. The obtained copolymer was characterized by 1H-NMR, and IR-spectrosco

ORGANIC SEMICONDUCTOR MATERIAL, PREPARATION METHODS AND USES THEREOF

-

Paragraph 0049; 0050; 0079-0081, (2013/11/19)

Disclosed are organic semiconductor material, preparation methods and uses thereof. The organic semiconductor material is shown as the following formula (P), in which R1, R2, R3, m, n, x and y are defined as the description. The said organic semiconductor material can be used in organic solar cell, organic field effect transistor, organic electroluminescence element, organic optical storage, organic non-linear material or organic laser element.

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