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749257

Sigma-Aldrich

2,2′-Bis[4-(trifluoromethyl)phenyl]-5,5′-bithiazole

97%

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About This Item

Empirische Formel (Hill-System):
C20H10F6N2S2
CAS-Nummer:
869896-76-4
Molekulargewicht:
456.43
MDL-Nummer:
MFCD22200513
UNSPSC-Code:
12352103
PubChem Substanz-ID:
329765976
NACRES:
NA.23

Assay

97%

Form

powder or crystals

mp (Schmelzpunkt)

230-235 °C

Halbleitereigenschaften

N-type (mobility=1.83 cm2/V·s)

SMILES String

FC(F)(F)c1ccc(cc1)-c2ncc(s2)-c3cnc(s3)-c4ccc(cc4)C(F)(F)F

InChI

1S/C20H10F6N2S2/c21-19(22,23)13-5-1-11(2-6-13)17-27-9-15(29-17)16-10-28-18(30-16)12-3-7-14(8-4-12)20(24,25)26/h1-10H

InChIKey

YPPDUFZJMJWOLJ-UHFFFAOYSA-N

Anwendung

This material is used as an n-type semiconductor for OFET devices. It forms a closely packed 2-dimensional columnar structure leading to a high performance n-type FET.[1]

Piktogramme

Skull and crossbones
GHS06

Signalwort

Danger

H-Sätze

H301,H319

Gefahreneinstufungen

Acute Tox. 3 Oral - Eye Irrit. 2

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

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Analysenzertifikate (COA)

Lot/Batch Number
MKBJ5137V

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Die Dokumentenbibliothek aufrufen

Shinji Ando et al.
Journal of the American Chemical Society, 127(43), 14996-14997 (2005-10-27)
Novel thiazole oligomers and thiazole/thiophene co-oligomers with trifluoromethylphenyl groups were developed as n-type semiconductors for OFETs. They showed excellent n-type performances with high electron mobilities. A 5,5'-bithiazole with trifluoromethylphenyl groups forms a closely packed two-dimensional columnar structure leading to a

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