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CAS

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628336-85-6

9-(2'-Ethylhexyl)-3-bromocarbazole is a chemical compound with the molecular formula C22H25BrN, derived from carbazole, a heterocyclic aromatic compound. It features a 2'-ethylhexyl group that enhances solubility in organic solvents and a bromine atom that imparts unique reactivity. 9-(2'-Ethylhexyl)-3-bromocarbazole is a crucial building block in the realm of organic electronics, particularly for the development of advanced optoelectronic devices.

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  • 628336-85-6 Structure

  • Basic information

    1. Product Name: 9-(2'-Ethylhexyl)-3-bromocarbazole
    2. Synonyms: 9-(2'-Ethylhexyl)-3-bromocarbazole;3-broMo-9-(2-ethylhexyl)-9H-carbazole
    3. CAS NO:628336-85-6
    4. Molecular Formula: C20H24BrN
    5. Molecular Weight: 358.31526
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 628336-85-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 462.4±27.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.23±0.1 g/cm3(Predicted)
    6. Refractive Index: 1.61
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 9-(2'-Ethylhexyl)-3-bromocarbazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9-(2'-Ethylhexyl)-3-bromocarbazole(628336-85-6)
    11. EPA Substance Registry System: 9-(2'-Ethylhexyl)-3-bromocarbazole(628336-85-6)

  • 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: 628336-85-6(Hazardous Substances Data)

628336-85-6 Usage

Uses

Used in Organic Electronics Industry:
9-(2'-Ethylhexyl)-3-bromocarbazole is used as a key component in the synthesis of organic light-emitting diodes (OLEDs) for its ability to facilitate the creation of efficient and durable light-emitting layers.
Used in Organic Photovoltaic Cells (OPVs) Manufacturing:
In the OPVs industry, 9-(2'-Ethylhexyl)-3-bromocarbazole is utilized as a material in the production of organic photovoltaic cells, contributing to the development of flexible and lightweight solar energy solutions.
Used as a Solvent-Soluble Compound:
Due to its solubility in organic solvents, 9-(2'-Ethylhexyl)-3-bromocarbazole is used as a processable material in thin film applications, allowing for the fabrication of electronic devices with precise layer control.
Used as a Halogenating Agent:
The bromine atom in 9-(2'-Ethylhexyl)-3-bromocarbazole's structure makes it a valuable halogenating agent in various chemical reactions, broadening its applications in synthetic chemistry and material science.

Check Digit Verification of cas no

The CAS Registry Mumber 628336-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,8,3,3 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 628336-85:
(8*6)+(7*2)+(6*8)+(5*3)+(4*3)+(3*6)+(2*8)+(1*5)=176
176 % 10 = 6
So 628336-85-6 is a valid CAS Registry Number.

628336-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-N-(2-ethylhexyl)carbazole

1.2 Other means of identification

Product number -
Other names 9-(2-ethylhexyl)-3-bromocarbazole

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:628336-85-6 SDS

628336-85-6Relevant articles and documents

4H-1,2,6-Thiadiazin-4-one-containing small molecule donors and additive effects on their performance in solution-processed organic solar cells

Hermerschmidt, Felix,Kalogirou, Andreas S.,Min, Jie,Zissimou, Georgia A.,Tuladhar, Sachetan M.,Ameri, Tayebeh,Faber, Hendrik,Itskos, Grigorios,Choulis, Stelios A.,Anthopoulos, Thomas D.,Bradley, Donal D. C.,Nelson, Jenny,Brabec, Christoph J.,Koutentis, Panayiotis A.

, p. 2358 - 2365 (2015/03/18)

The optical, electrochemical, morphological and transport properties of a series of thiadiazinone (acceptor) and (thienyl)carbazoles (donor) containing π-extended donor-acceptor-donors (D-A-D) are presented. Systematic variations in the number of the thienyl units, the choice of branched or straight alkyl side chains and the use of a processing additive demonstrate their use as electron donors in bulk heterojunction solar cells blended with fullerene acceptors. The best power conversion efficiency (PCE) of 2.7% is achieved by adding to the D-A-D 3:fullerene blend a polydimethylsiloxane (PDMS) additive, that improves the morphology and doubles the hole mobility within the D-A-D:fullerene blend.

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