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Merck
CN

749257

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

97%

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关于此项目

经验公式(希尔记法):
C20H10F6N2S2
化学文摘社编号:
分子量:
456.43
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
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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

SMILES string

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

InChI key

YPPDUFZJMJWOLJ-UHFFFAOYSA-N

assay

97%

form

powder or crystals

mp

230-235 °C

semiconductor properties

N-type (mobility=1.83 cm2/V·s)

Application

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.

pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2

存储类别

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

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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

商品

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