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(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 866100-14-3 Structure
  • Basic information

    1. Product Name: (9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid
    2. Synonyms: BORONIC ACID, (9,9-DIMETHYL-9H-FLUORENE-2,7-DIYL)BIS;(9,9-dimethyl-9H-fluorene-2,7-diyl)bisboronic acid;Boronicacid,(9,9-dimethyl-9H-fluorene-2,7-diyl)b;(9,9-DIMETHYL-9H-FLUOROENE-2,7-DIYL)BISBORONIC ACID;(9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid;BORONIC ACID, (9,9-DIMETHYL-9H-FLUORENE-2,7-DIYL)BIS- (9CI);9,9-Dimethyl-9H-fluoren-2,7-diyl-2,7-diboronic acid;(9,9-Dimethyl-9H-flu
    3. CAS NO:866100-14-3
    4. Molecular Formula: C15H16B2O4
    5. Molecular Weight: 281.91
    6. EINECS: 1312995-182-4
    7. Product Categories: Boron Compounds;Electronic Chemicals;OLED materials,pharm chemical,electronic;OLED materrials
    8. Mol File: 866100-14-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 569.7 °C at 760 mmHg
    3. Flash Point: 298.3 °C
    4. Appearance: /
    5. Density: 1.32 g/cm3
    6. Vapor Pressure: 8.12E-14mmHg at 25°C
    7. Refractive Index: 1.635
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: (9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid(866100-14-3)
    12. EPA Substance Registry System: (9,9-Dimethyl-9H-fluoren-2,7-diyl)diboronic acid(866100-14-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 866100-14-3(Hazardous Substances Data)

866100-14-3 Usage

Chemical Properties

Off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 866100-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,1,0 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 866100-14:
(8*8)+(7*6)+(6*6)+(5*1)+(4*0)+(3*0)+(2*1)+(1*4)=153
153 % 10 = 3
So 866100-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H16B2O4/c1-15(2)13-7-9(16(18)19)3-5-11(13)12-6-4-10(17(20)21)8-14(12)15/h3-8,18-21H,1-2H3

866100-14-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (9,9-Dimethyl-9H-fluorene-2,7-diyl)diboronic acid

1.2 Other means of identification

Product number -
Other names (7-borono-9,9-dimethylfluoren-2-yl)boronic 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:866100-14-3 SDS

866100-14-3Downstream Products

866100-14-3Relevant articles and documents

Dibenzocarbazole fused ring compound and organic electroluminescent device thereof

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Paragraph 0093-0095, (2018/03/06)

The invention provides a dibenzocarbazole fused ring compound and an organic electroluminescent device thereof, and relates to the technical field of an organic optoelectronic material. A carbazoles structure is relatively high in redox potential value and excellent in stability in an air or lighting condition. Through introduction of a fused-ring rigid asymmetric and dense structure, the obtainedaromatic amines derivative is improved in thermal stability. The compound is used to prepare an organic electroluminescent device. Specifically, when the compound is taken as a main material in the organic electroluminescent device, the carbazoles main material having a rigid structure is high in glass-transition temperature, which is beneficial for prolonging the life of the organic electroluminescent device. The organic electroluminescent device shows high efficiency and low driving voltage, is not prone to crystallize, and is superior to a common OLED device.

Aromatic amine derivative as well as preparation method and application thereof

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Paragraph 0047; 0048; 0049; 0050, (2017/07/19)

The invention provides an aromatic amine derivative as well as a preparation method and application thereof, and relates to the technical field of organic photoelectric materials. By introducing a fluorenylidene, subindenofluorene or spirobifluorene structure, the conjugation degree of a system is improved, and the thermal stability of the aromatic amine derivative obtained by the invention is enabled to be high; the aromatic amine derivative can be used for producing an organic electroluminescence device, particularly can serves as a hole-transport material in the organic electroluminescence device and shows the advantages of high luminous efficiency and long service life; the organic electroluminescence device produced by using the aromatic amine derivatives is superior to a common OLED (Organic Light Emitting Diode) device. The invention also provides the preparation method of the aromatic amine derivatives, which is simple; raw materials are easy to obtain.

Fluorene-based boronic acids as fluorescent chemosensor for monosaccharides at physiological pH

Hosseinzadeh, Rahman,Mohadjerani, Maryam,Pooryousef, Mona

, p. 549 - 555 (2015/12/04)

Two fluorene-based boronic acids, 9,9-dimethyl-9H-fluoren-2-yl-2-boronic acid (1) and 9,9-dimethyl-9H-fluoren-2,7-diyl-2,7-diboronic acid (2), were synthesized and their sensing abilities for detection of D-monosaccharides were investigated by fluorescence at physiological pH. It was found that both boronic acids 1 and 2 have high selectivity and sensitivity for D-fructose with stability constant of 47.2 and 412.9, respectively. The sensor 2 showed a linear response toward D-fructose in the concentration range from 5 × 10-5 to 10-1 mol L-1 with the detection limit of 2 × 10-5 mol L-1.

Nitrogenous heterocyclic derivative and organic electroluminescence device making use of the same

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Page/Page column 43-44, (2011/11/30)

A novel nitrogen-containing heterocyclic compound having a specific structure and an organic electroluminescence device comprising an anode, a cathode and an organic thin film layer which comprises a single layer or a plurality of layers comprising at least a light emitting layer and is disposed between the anode and the cathode, wherein at least one layer in the organic thin film layer comprises the above nitrogen-containing heterocyclic derivative singly or as a component of a mixture. The organic electroluminescence device exhibits a great luminance of emitted light and a great efficiency of light emission even under application of a low voltage.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENCE DEVICE UTILIZING THE SAME

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Page/Page column 21; 22, (2008/06/13)

Provided is a novel aromatic amine derivative with specified structure. Also provided is an organic electroluminescence device having one or more organic thin-film layers including at least a luminescent layer interposed between a cathod and an anode, in which at least one of the organic thin-film layers contains the above aromatic amine derivative alone or as a component of mixture. As a result, there is provided an organic electroluminescence device that has high emission luminance and high heat resistance, excelling in high-temperature storage ability and has long life, and provided an aromatic amine derivative for realizing the organic electroluminescence device.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENCE DEVICE UTILIZING THE SAME

-

Page/Page column 32; 33, (2008/06/13)

A novel aromatic amine derivative with specified structure. Further, there is provided an organic electroluminescence device having one or more organic thin-film layers including at least a luminescent layer interposed between a negative electrode and a positive electrode, wherein at least one of the organic thin-film layers contains the above aromatic amine derivative alone or as a component of mixture. As a result, there is provided an organic electroluminescence device that has high emission luminance and high heat resistance, excelling in high-temperature storability and has long life, and provided an aromatic amine derivative for realization of the organic electroluminescence device.

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