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About This Item
經驗公式（希爾表示法）:
C5H6OS
CAS號碼:
分子量：:
114.17
Beilstein:
106404
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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推薦產品
化驗
98%
形狀
liquid
折射率
n20/D 1.532 (lit.)
bp
80-82 °C/65 mmHg (lit.)
密度
1.143 g/mL at 25 °C (lit.)
SMILES 字串
COc1ccsc1
InChI
1S/C5H6OS/c1-6-5-2-3-7-4-5/h2-4H,1H3
InChI 密鑰
RFSKGCVUDQRZSD-UHFFFAOYSA-N
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一般說明
3-Methoxythiophene is a thiophene. The intramolecular and intermolecular geometries of crystals of 3-methoxythiophene were studied.[1] Spectroscopic studies of bipolarons derived from oligomerized 3-methoxythiophene in solution has been reported.[2] The electropolymerization of 3-methoxythiophene on Pt and Fe electrodes in an aqueous micellar medium containing sodium dodecyl sulfate and 10-3M bithiophene has been reported.[3] Thin polymer films of 3-methoxythiophene at the cathode in a direct current discharge have been prepared.[4]
訊號詞
Warning
危險聲明
危險分類
Flam. Liq. 3
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
120.2 °F - closed cup
閃點（°C）
49 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Chirality, 32(12), 1361-1376 (2020-11-17)
Novel optically active oligothiophenes bearing electron-donating chiral side chains have been prepared by synthetic methods suitable to achieve regioregular head-to-tail and head-to-head/tail-to-tail derivatives. In particular, the chiral (S)-(2-methyl)butyl moiety was linked at position 3 of the thiophene ring through heteroatoms
Paolo Bollella et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 21(1), 120-128 (2019-08-14)
Biocatalytic buckypaper electrodes modified with pyrroloquinoline quinone (PQQ)-dependent glucose dehydrogenase and bilirubin oxidase for glucose oxidation and oxygen reduction, respectively, were prepared for their use in a biofuel cell. A small (millimeter-scale; 2×3×2 mm3 ) enzyme-based biofuel cell was tested in
Electrosynthesis and characterization of poly (3-methoxythiophene)-polybithiophene composite films prepared in micellar media on Pt and Fe substrates.
Dieng MaM, et al.
Physical Chemistry Chemical Physics, 1(8), 1731-1734 (1999)
Spectroscopic studies of bipolarons from oligomerized 3-methoxythiophene in solution.
Chang A-C and Miller LL.
Synthetic Metals, 22(1), 71-78 (1987)
Blake et al.
Acta crystallographica. Section B, Structural science, 55(Pt 6), 963-974 (2000-08-06)
The intramolecular and intermolecular geometries of six thiophenes carrying oxygen-containing substituents have been determined. Crystals of 2-methoxythiophene and 3-methoxythiophene were grown in situ on a diffractometer from liquid samples. The 2-methoxy group introduces significant distortions to the thiophene nucleus and
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