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9-Phenanthracenylboronic acid is an organic compound characterized by its unique boron-containing structure, which is derived from phenanthrene. 9-Phenanthracenylboronic acid exhibits fluorescent properties and is known for its reactivity in chemical reactions, particularly in the field of organic synthesis.

68572-87-2

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68572-87-2 Usage

Uses

Used in Analytical Chemistry:
9-Phenanthracenylboronic acid is used as a fluorescent analytical reagent for glucose-specific detection in sensing systems. Its fluorescent properties allow for the selective and sensitive detection of glucose, making it a valuable tool in analytical chemistry for monitoring glucose levels in various applications.
Used in Organic Synthesis:
In the field of organic synthesis, 9-Phenanthracenylboronic acid is utilized as a reagent in the Suzuki reaction. The Suzuki reaction is a widely used cross-coupling reaction in organic chemistry that facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules. The use of 9-Phenanthracenylboronic acid in this reaction highlights its importance in the synthesis of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 68572-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,5,7 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68572-87:
(7*6)+(6*8)+(5*5)+(4*7)+(3*2)+(2*8)+(1*7)=172
172 % 10 = 2
So 68572-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H11BO2/c16-15(17)14-9-10-5-1-2-6-11(10)12-7-3-4-8-13(12)14/h1-9,16-17H

68572-87-2 Well-known Company Product Price

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  • TCI America

  • (P1093)  9-Phenanthreneboronic Acid (contains varying amounts of Anhydride)  

  • 68572-87-2

  • 1g

  • 350.00CNY

  • Detail
  • TCI America

  • (P1093)  9-Phenanthreneboronic Acid (contains varying amounts of Anhydride)  

  • 68572-87-2

  • 5g

  • 850.00CNY

  • Detail
  • Alfa Aesar

  • (H52546)  Phenanthrene-9-boronic acid, 97%   

  • 68572-87-2

  • 1g

  • 348.0CNY

  • Detail
  • Alfa Aesar

  • (H52546)  Phenanthrene-9-boronic acid, 97%   

  • 68572-87-2

  • 5g

  • 1389.0CNY

  • Detail

68572-87-2SDS

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 9-Phenanthreneboronic Acid

1.2 Other means of identification

Product number -
Other names phenanthren-9-ylboronic 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:68572-87-2 SDS

68572-87-2Relevant academic research and scientific papers

Synthesis and luminescent properties of poly(9-(3-Vinyl-phenyl)-phenanthrene)

Yang, Garam,Lee, Hayoon,Lee, Suji,Jung, Hyocheol,Shin, Hwangyu,Lee, Jaehyun,Park., Jongwook

, p. 1748 - 1751 (2016)

Recently, interest of polymer light-emitting diode (PLED) fabricated from conjugated polymer has augmented because PLED has advantage property that is well-suited to flexible lighting and solution processed device. In this presentation, we suggest a new polymer host based on phenanthrene, poly(9-(3-Vinyl-phenyl)-phenanthrene) (PVPP). It can be easily synthesized through simple synthetic methods which are Suzuki and Wittig reactions. PVPP film can be obtained from spin coating with solution used by common solvent. It exhibited PL maximum value of 381 nm and broad PL spectrum. Energy transfer smoothly occurred when the three dopants for green, red and yellow were used in PVPP.

Preparation method of dibenzo [g,p] condensed naphthalene compound

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Paragraph 0108-0111, (2020/03/25)

The invention relates to the field, of organic synthesis, and particularly relates to a preparation method [g,p] of a dibenzo. condensed naphthalene compound 1, and the preparation method, of the compound of Formula: comprises 7 reacting the compound of Formula, in the presence of an inorganic Lewis acid and an oxidizing agent to obtain a compound 1 of Formula. The present invention provides a method for preparing a dibenzo [g,p] fused bicyclic naphthalene compound according to the present invention by using an inorganic Lewis acid and an oxidizing agent to, prepare a compound of, the, present invention having a high overall, conversion rate, and, a high efficiency . industrial production operation .

Aromatic amine derivatives having fluorenyl moiety and organic light-emitting diode including the same

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Paragraph 0215-0221, (2020/03/24)

The present invention relates to aromatic amine derivatives with a fluorene structure and a light-emitting element including the same, and more specifically, to an organic light-emitting compound expressed as [Formula A] and a light-emitting element containing the same. [Formula A] In [Formula A], X1 or X8 and Ar1, Ar2 are specifically defined in the description of the invention.

Phosphorescence host material and application thereof in organic electroluminescence devices

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Paragraph 0052; 0054-0057, (2019/10/15)

The invention relates to an organic compound; the organic compound is as shown in a formula (1), and the formula (1) is described in the description, wherein the dotted circle represents a benzene ring structure, and indole derivative groups positioned at the two sides of the benzene ring structure are fused into indolocarbazole derivatives by means of the benzene ring structure; X1-X8 is CR or N;one of Ar1 and Ar2 is selected from pi-absence electron-type aromatic groups of C3-C30; R is selected from hydrogen, aliphatic hydrocarbon groups of C1-C4, aryl groups of C6-C30 and heteroaryl groupsof C3-C30; when multiple Rs exist, all the Rs can be the same or different; m and n are respectively integers within a range of 1-4; p is 1 or 2; L1 and L2 are respectively and independently selectedfrom a single bond, arylene groups of C6-C12 or hetero-arylene groups of C3-C12; when substituents exist in the groups, the substituents are respectively and independently selected from halogen, alkyl or cycloalkyl groups of C1-C10, alkenyl or cycloalkenyl groups of C2-C6, alkoxy or thioalkoxy groups of C1-C6, monocyclic aryl or fused ring aryl groups of C6-C30, monocyclic heteroaryl or fused ring heteroaryl groups of C3-C30, or a combined structure of the groups.

Naphtho-fluorene carbazole compound and application thereof

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Paragraph 0086; 0089-0091, (2018/03/26)

The invention belongs to the field of organic electroluminescence, and in particular relates to a naphtho-fluorene carbazole compound and application thereof. An OLED device manufactured by taking thesynthesized organic compound as a main body light-emitting material can be applied in the fields of AM drive OLED display, PM drive OLED display or OLED illumination. The external quantum efficiency,the power efficiency and the current efficiency of the device are greatly improved, and the service life of the device is obviously prolonged, so that the naphtho-fluorene carbazole compound has thegood market prospect.

aromatic compound having fused cyclic substituent in aromatic ring and organic light-emitting diode including the same

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Paragraph 0412-0417, (2019/01/06)

The present invention relates to a compound having a cyclic substituent fused with a cyclic ring and an organic light emitting diode including the same, and more particularly, to a compound for an organic light emitting diode represented by chemical formula A and an organic light emitting diode including the same. In chemical formula A, X is a substituent having structural formula X, Y is a substituent of structural formula Y1, n is an integer from 1 to 4, and structural formulas X and Y1 are the same as described in detailed description of the present invention.

Pyrene-contained compound and organic light-emitting device

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Paragraph 0037; 0038; 0039; 0040, (2017/12/27)

The invention provides a pyrene-contained compound and an organic light-emitting device prepared therefrom, belongs to the technical field of organic photoelectric materials, and solves the technical problems in the prior art that the organic photoelectric materials have poor light-emitting properties such as low light-emitting efficiency, relatively high driving voltage, short service life and the like. Compared with the prior art, the organic light-emitting device prepared from the pyrene-contained compound provided by the invention has the advantage of obviously improved light-emitting properties; the pyrene-contained compound is an excellent OLED (organic light-emitting device) material.

4 containing substituent at the 2 - (2' - hydroxy phenyl) benzoxazole compound and its preparation and use (by machine translation)

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Paragraph 0040; 0044, (2017/07/11)

The invention relates to the organic semiconductor field of photoelectric technology, provides a 4 containing substituent at the 2 - (2' - hydroxy phenyl) benzoxazole compound and its preparation and use. The 4 containing substituent at the 2 - (2' - hydroxy phenyl) benzoxazole compounds of the general formula: Wherein X is S, O or NH, Ar containing aromatic conjugated structure unit. The compound is 2 - (2' - 4 - bromophenol) benzoxazole with belt bromine of the polycyclic aromatic hydrocarbon compound prepared by Suzuki reaction. The invention compounds of this invention have potentional intramolecular proton transfer compound four-level transition fluorescent nature, can be used as a luminescent material, is used for the light-emitting diode component in machine is white. The compounds of the invention has: a large storck displacement, the good light-emitting quantum efficiency, simple preparation, synthetic high yield and the like. (by machine translation)

BLUE FLUORESCENT HOST MATERIALS, AND ORGANIC THIN FILM AND ORGANIC LIGHT EMITTING DEVICES COMPRISING THE SAME

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Paragraph 0123-0121, (2017/06/19)

The present invention provides an organic compound represented by chemical formula 1, and an organic electroluminescent device comprising the same. The present invention comprises a blue fluorescent host material, thereby providing the organic electroluminescent device having improved driving voltage, light-emitting efficiency, and light-emitting lifespan.COPYRIGHT KIPO 2017

Phosphoryl substituted triazine derivatives and organic electroluminescent device including the same

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Paragraph 0105-0107, (2017/01/26)

The present invention relates to phosphoryl group bonded triazine derivatives represented by chemical formulas 1 and 2. In the chemical formulas 1 and 2, the definitions of the substituent groups are the same as defined in the specification. The triazine derivatives have excellent current density and durability in comparison to a conventional material. The organic electroluminescent device has reduced driving voltage, improved luminous efficiency, and extended lifespan.COPYRIGHT KIPO 2016

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