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Merck
CN

T31801

噻吩

≥99%

别名:

硫代呋喃, 硫杂茂

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关于此项目

经验公式(希尔记法):
C4H4S
化学文摘社编号:
分子量:
84.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-729-4
Beilstein/REAXYS Number:
103222
MDL number:
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产品名称

噻吩, ≥99%

InChI key

YTPLMLYBLZKORZ-UHFFFAOYSA-N

InChI

1S/C4H4S/c1-2-4-5-3-1/h1-4H

SMILES string

c1ccsc1

vapor density

2.9 (vs air)

vapor pressure

40 mmHg ( 12.5 °C)

assay

≥99%

autoignition temp.

743 °F

expl. lim.

12.5 %

refractive index

n20/D 1.529 (lit.)

bp

84 °C (lit.)

mp

−38 °C (lit.)

density

1.051 g/mL at 25 °C (lit.)

Quality Level

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Application

噻吩是合成各种共轭有机硫部分、含硫多环芳烃、大环化合物和药物化合物的重要前体。它已被广泛用于合成聚噻吩和用于有机场效应晶体管(OFET)和有机太阳能电池(OSC)的大量活性材料。

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 2

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

15.8 °F

flash_point_c

-9 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Thiophene-based push-pull chromophores for small molecule organic solar cells (SMOSCs)
Malytskyi V, et al.
Royal Society of Chemistry Advances, 5(1), 354-397 (2015)
Construction of synthetic macrocyclic compounds possessing subheterocyclic rings, specifically pyridine, furan, and thiophene.
Newkome GR, et al.
Chemical Reviews, 77(4), 513-597 (1977)
Solution-processed and high-performance organic solar cells using small molecules with a benzodithiophene unit.
Zhou J, et al.
Journal of the American Chemical Society, 135(23), 8484-8487 (2013)
Sukyoung Hwang et al.
Scientific reports, 5, 11201-11201 (2015-06-19)
The growth kinetics of polymer thin films prepared by plasma-based deposition method were explored using atomic force microscopy. The growth behavior of the first layer of the polythiophene somewhat differs from that of the other layers because the first layer
Sang-Eun Bae et al.
Journal of colloid and interface science, 456, 93-99 (2015-06-24)
A very simple preparation was developed for catalytically active Pd-nanoparticles (Pd-NPs) decorating polythiophene conducting polymer nanospheres by the redox reaction between PdCl4(2-) ion and 2-thiophenemethanol (2-TPM) in an aqueous solution at room temperature. 2-TPM polymerized to form polythiophene nanospheres in

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