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9-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is a carbazole derivative featuring a carbazole core with two boronic acid pinacol ester groups at the 2nd and 7th positions. This chemical compound is known for its high thermal stability, good charge transport properties, and tunable energy levels, making it a promising candidate for applications in organic electronics and optoelectronics.

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  • 406726-92-9 Structure
  • Basic information

    1. Product Name: 9-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
    2. Synonyms: 9-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole;9-Octylcarbazole-2,7-diboronic acid dipinacol ester;N-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole;2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-N-9-octylcarbazole;9-Dioctylcarbazole-2,7-Bis(Bronic acid pinacol ester);9-n-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole;9-n-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole;9H-Carbazole, 9-octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
    3. CAS NO:406726-92-9
    4. Molecular Formula: C32H47B2NO4
    5. Molecular Weight: 531
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 406726-92-9.mol
  • Chemical Properties

    1. Melting Point: 168-169℃
    2. Boiling Point: 608.8±48.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.05
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 9-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(406726-92-9)
    11. EPA Substance Registry System: 9-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole(406726-92-9)
  • 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: 406726-92-9(Hazardous Substances Data)

406726-92-9 Usage

Uses

Used in Organic Electronic Materials:
9-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is used as a key component in organic electronic materials for its high thermal stability, good charge transport properties, and tunable energy levels.
Used in Organic Light-Emitting Diodes (OLEDs):
In the OLED industry, 9-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is used as a material for enhancing the performance and efficiency of light-emitting devices due to its desirable electronic properties.
Used in Organic Photovoltaics (OPVs):
9-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is utilized in the development of organic photovoltaics, where it contributes to improving the efficiency and stability of solar cells by leveraging its charge transport characteristics and energy level tunability.

Check Digit Verification of cas no

The CAS Registry Mumber 406726-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,7,2 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 406726-92:
(8*4)+(7*0)+(6*6)+(5*7)+(4*2)+(3*6)+(2*9)+(1*2)=149
149 % 10 = 9
So 406726-92-9 is a valid CAS Registry Number.

406726-92-9 Well-known Company Product Price

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  • TCI America

  • (O0439)  9-n-Octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole  >97.0%(HPLC)(N)

  • 406726-92-9

  • 200mg

  • 1,190.00CNY

  • Detail

406726-92-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-octyl-2,7-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole

1.2 Other means of identification

Product number -
Other names 2,5-DIMETHYL-3-PYRROLINE

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:406726-92-9 SDS

406726-92-9Relevant articles and documents

Organic fluorescent sensing material capable of selectively detecting nerve agent, and preparation method and application thereof

-

Paragraph 0150; 0152, (2018/01/09)

The invention belongs to the field of organic semiconductor nanomaterials, and concretely relates to an organic fluorescent sensing material capable of selectively detecting a nerve agent, and a preparation method and application thereof. The invention prepares the organic fluorescent sensing material capable of selectively detecting the nerve agent. A series of P type organic fluorescent sensing materials based on carbazole molecules synthesize to form a structure of a carbazole derivative with different side chains through changing side chains of the carbazole molecules and a polymerization degree thereof, and a one-dimensional organic semiconductor nanowire is obtained through a self-assembly method, namely the organic fluorescent sensing material capable of selectively detecting the nerve agent. The nanowire provided by the invention has the characteristics of large specific surface area, more surface porosity and the like, the nerve agent to be detected is favorably adsorbed and diffused on the surface of the nanowire, and a detection limit is greatly reduced. Therefore, the organic fluorescent sensing material provided by the invention can be used as a fluorescence sensor with an excellent performance capable of recognizing the nerve agent.

Organic fluorescence sensing composite material with ultrahigh sensitivity response for explosives as well as preparation and application thereof

-

Paragraph 0137; 0139; 0141, (2018/01/04)

The invention relates to an organic fluorescence sensing composite material with ultrahigh sensitivity response for explosives as well as preparation and application thereof. The material is a blended one-dimensional organic semiconductor nanowire obtained by compositing one or more metallorganics complexes based on carbazole molecules and an organic fluorescence sensing material based on a series of carbazole molecules by a self-assembly method; the material has the characteristics of being porous, being large in superficial area, high in fluorescence quantum efficiency, uniform in mixing and the like, is suitable for fluorescence detection for the explosives and is particularly very efficient in detection for trace explosives.

Conjugated ladder-type heteroacenes bearing pyrrole and thiophene ring units: Facile synthesis and characterization

Gao, Peng,Feng, Xinliang,Yang, Xiaoyin,Enkelmann, Volker,Baumgarten, Martin,Muellen, Klaus

scheme or table, p. 9207 - 9213 (2009/04/11)

(Chemical Equation Presented) Ladder-type heteroacenes containing pyrrole and thiophene rings, dibenzo[b,b′]thieno[2,3-f:5,4-f′]-carbazoles (DBTCZ, 1), and diindolo[3,2-b:2′,3′-h]benzo[1],2-b:4,5-b′] bis[1]benzothiophene (DIBBBT, 2), were facilely synthes

Synthesis of diindolocarbazoles by cadogan reaction: Route to ladder oligo(p-aniline)s

Bouchard, Jimmy,Wakim, Salem,Leclerc, Mario

, p. 5705 - 5711 (2007/10/03)

Symmetric and nonsymmetric diindolocarbazoles were successfully synthesized for the first time by a Cadogan ring closure using N-alkyl-2,7-disubstituted carbazole precursors. Cyclization reaction on N-alkyl-2,7-di(2′- nitrophenyl) carbazole derivatives is

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