Key Documents

View All Documentation

757179

1,2,3,4,5,6,7,8-Octafluoro-9,10-bis[4-(trifluoromethyl)phenyl]anthracene

Name: 1,2,3,4,5,6,7,8-Octafluoro-9,10-bis[4-(trifluoromethyl)phenyl]anthracene
Brand: ALDRICH

97%

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):

C₂₈H₈F₁₄

CAS Number:

1067426-44-1

Molecular Weight:

610.34

NACRES:

NA.23

PubChem Substance ID:

329766653

UNSPSC Code:

12352103

MDL number:

MFCD22200543

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

assay

97%

form

powder

mp

300-310 °C

orbital energy

HOMO 6.02 eV (CV), LUMO 3.14 eV (CV)

SMILES string

Fc1c(F)c(F)c2c(-c3ccc(cc3)C(F)(F)F)c4c(F)c(F)c(F)c(F)c4c(-c5ccc(cc5)C(F)(F)F)c2c1F

InChI

1S/C28H8F14/c29-19-15-13(9-1-5-11(6-2-9)27(37,38)39)16-18(22(32)26(36)24(34)20(16)30)14(17(15)21(31)25(35)23(19)33)10-3-7-12(8-4-10)28(40,41)42/h1-8H

InChI key

FFUQDRYCGMPMRR-UHFFFAOYSA-N

Description

Application

This material is a relatively new candidate as a n-type semiconductor for use in Organic Field Effect Transistor (OFET) devices

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

MKBK1361

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Articles

Development of Small Molecule Donors for Solution-Processed Organic Solar Cells

Solution-processed organic photovoltaic devices (OPVs) have emerged as a promising clean energy generating technology due to their ease of fabrication, potential to enable low-cost manufacturing via printing or coating techniques, and ability to be incorporated onto light weight, flexible substrates.

Organic Transistors for Biomedical Applications

Thin, lightweight, and flexible electronic devices meet widespread demand for scalable, portable, and robust technology.

Soluble Pentacene Precursors

Fabrication procedure of organic field effect transistor device using a soluble pentacene precursor.

9,10-Disubstituted octafluoroanthracene derivatives via palladium-catalyzed cross-coupling.

John F Tannaci et al.

The Journal of organic chemistry, 73(20), 7895-7900 (2008-09-16)

9,10-Dichlorooctafluoroanthracene (1) reacts with aryl boronic acids and terminal alkynes under palladium-catalyzed cross-coupling conditions to afford 9,10-diaryloctafluoroanthracenes (2a-e) and 9,10-dialkynyloctafluoroanthracenes (6a,b), respectively. Optical spectroscopy and cyclic voltammetry indicate that octafluoro-9,10-di(thiophen-2-yl)anthracene (2d) exhibits donor-acceptor character and a LUMO energy level of

Global Trade Item Number

SKU	GTIN
757179-1G	04061826242643