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302554-81-0

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  • High Quality 99% 302554-81-0 2-(9,9-Dioctyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Manufacturer

    Cas No: 302554-81-0

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302554-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 302554-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,5,5 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 302554-81:
(8*3)+(7*0)+(6*2)+(5*5)+(4*5)+(3*4)+(2*8)+(1*1)=110
110 % 10 = 0
So 302554-81-0 is a valid CAS Registry Number.
InChI:InChI=1S/C35H55BO3/c1-7-9-11-13-15-19-25-35(26-20-16-14-12-10-8-2)31-22-18-17-21-29(31)30-24-23-28(27-32(30)35)36(38)39-34(5,6)33(3,4)37/h17-18,21-24,27,37-38H,7-16,19-20,25-26H2,1-6H3

302554-81-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H51953)  9,9-Di-n-octylfluorene-2-boronic acid pinacol ester, 95%   

  • 302554-81-0

  • 1g

  • 414.0CNY

  • Detail
  • Alfa Aesar

  • (H51953)  9,9-Di-n-octylfluorene-2-boronic acid pinacol ester, 95%   

  • 302554-81-0

  • 5g

  • 1725.0CNY

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  • Aldrich

  • (723630)  9,9-Dioctylfluorene-2-boronic acid pinacol ester  95%

  • 302554-81-0

  • 723630-1G

  • 1,185.21CNY

  • Detail
  • Aldrich

  • (723630)  9,9-Dioctylfluorene-2-boronic acid pinacol ester  95%

  • 302554-81-0

  • 723630-5G

  • 3,628.17CNY

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302554-81-0SDS

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-dioctylfluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names RB2069

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:302554-81-0 SDS

302554-81-0Relevant articles and documents

Conjugated diene monomer 9-9 - dialkyl fluorene as structural unit and synthesis method thereof

-

, (2021/10/05)

The invention relates to a conjugated diene monomer 9-9 - dialkyl fluorene as a structural unit and a synthesis method thereof, and belongs to the technical field of organic synthesis. 9, 9 - Dialkyl fluorene is the structural unit of the conjugated diene monomer. Herein R is a linear or branched alkyl group having a different number (6 - 30) of carbon atoms, n Shows functional groups of each intermediate, and a functional ethylenic monomer with Suzuki and 9 dialkyl fluorene as a core with different conjugation lengths can be obtained by repeating the bromination and acetylation reduction of the fluorene or 9 - fluorene oligomer. The problem of flexible expansion of chemical reaction of organic small molecules of fluorene units can be solved.

Bipolar small-molecule luminescent material adopting aromatic heterocyclicindenofluorene unit as core as well as preparation method and application of bipolar small-molecule luminescent material

-

, (2017/08/19)

The invention discloses a bipolar small-molecule luminescent materialadopting an aromatic heterocyclicindenofluorene unit as a core as well as a preparation method and an application of the bipolar small-molecule luminescent material. The bipolar small-molecule luminescent material adopting the aromatic heterocyclicindenofluorene unit as the core is prepared through a Suzuki polymerization reaction, the synthetic method is simple, purification is easy, and industrial application is facilitated. The bipolar small-molecule luminescent material adopting the aromatic heterocyclicindenofluorene unit as the core is better in aromatic heterocyclicindenofluorene planarity and has higher fluorescence quantum yield; meanwhile, the bipolar small-molecule luminescent material adopting the aromatic heterocyclicindenofluorene unit as the core has good solubility, film-forming property and film morphology stability, is suitable for solution processing and printing display and is used for preparation of a luminescent layer of an organic light emitting diode, and annealing treatment is not needed when the luminescent layer based on the bipolar small-molecule luminescent material is used for preparing a device, so that the preparation process is simple.

Benzobisoxazole cruciforms: A tunable, cross-conjugated platform for the generation of deep blue OLED materials

Chavez, Ramiro,Cai, Min,Tlach, Brian,Wheeler, David L.,Kaudal, Rajiv,Tsyrenova, Ayuna,Tomlinson, Aimée L.,Shinar, Ruth,Shinar, Joseph,Jeffries-El, Malika

, p. 3765 - 3773 (2016/05/24)

Four new cross-conjugated small molecules based on a central benzo[1,2-d:4,5-d′]bisoxazole moiety possessing semi-independently tunable HOMO and LUMO levels were synthesized and the properties of these materials were evaluated experimentally and theoretically. The molecules were thermally stable with 5% weight loss occurring well above 350 °C. The cruciforms all exhibited blue emission in solution ranging from 433-450 nm. Host-guest OLEDs fabricated from various concentrations of these materials using the small molecule host 4,4′-bis(9-carbazolyl)-biphenyl (CBP) exhibited deep blue-emission with Commission Internationale de L'Eclairage (CIE) coordinates of (0.15 ≤ x ≤ 0.17, 0.05 ≤ y ≤ 0.11), and maximum luminance efficiencies as high as ~2 cd A-1. These results demonstrate the potential of benzobisoxazole cruciforms as emitters for developing high-performance deep blue OLEDs.

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