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:
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。
signalword
Danger
hcodes
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
此项目有
Construction of synthetic macrocyclic compounds possessing subheterocyclic rings, specifically pyridine, furan, and thiophene.
Newkome GR, et al.
Chemical Reviews, 77(4), 513-597 (1977)
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)
Thiophene Polymer Semiconductors for Organic Thin-Film Transistors
Ong BS, et al.
Chemistry?A European Journal , 14(16), 4766-4778 (2008)
Thiophene, Benzo [b] thiophene and Dibenzo [b, d] thiophene as Precursors to Highly Conjugated Organosulfur Compounds.
Bianchini, Claudio and Meli, Andrea
Synlett, 1997(06), 643-649 (1997)
Palladium-Catalyzed Decarboxylative C-H Bond Arylation of Thiophenes.
Hu P and Zhang M
Angewandte Chemie (International Edition in English), 124(1), 231-235 (2012)
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