蒸汽压
0.31 mmHg ( 20 °C)
质量水平
检测方案
98%
形式
liquid
自燃温度
>392 °F
折射率
n20/D 1.583 (lit.)
bp
194-196 °C (lit.)
86-87 °C/20 mmHg (lit.)
密度
1.28 g/mL at 25 °C (lit.)
储存温度
2-8°C
SMILES字符串
[H]C(=O)c1ccsc1
InChI
1S/C5H4OS/c6-3-5-1-2-7-4-5/h1-4H
InChI key
RBIGKSZIQCTIJF-UHFFFAOYSA-N
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应用
3-噻吩甲醛已用于合成：
- 一系列 4-取代 2-噻吩磺酰胺
- 4′-去甲基表鬼臼毒素-β-D-葡萄糖苷和表鬼臼毒素-β-D-葡萄糖苷的缩醛和缩酮衍生物
- 1,2-二-3-噻吩基-2-羟基乙酮（3,3′-荆芥），安息香的 3-噻吩基对称类似物
R S Gupta et al.
Anti-cancer drug design, 2(1), 1-12 (1987-08-01)
We have synthesized acetal and ketal derivatives of 4'-demethylepipodophyllotoxin-beta-D-glucoside (DMEPG) and epipodophyllotoxin-beta-D-glucoside (EPG) with a number of different aldehydes (viz. acetaldehyde, propionaldehyde, 2-thiophenecarboxaldehyde, 3-thiophenecarboxaldehyde, 2-furancarboxaldehyde, benzaldehyde, phenylacetaldehyde, hydrocinnamaldehyde) and acetone. The cross resistance of these compounds towards a set of
J M Holmes et al.
Journal of medicinal chemistry, 37(11), 1646-1651 (1994-05-27)
A series of 4-substituted 2-thiophenesulfonamides was prepared from 3-thiophenecarboxaldehyde using metalation chemistry developed for 3-furaldehyde. Several of these compounds inhibit carbonic anhydrase II in vitro at concentrations of less than 10 nM. In addition, none of these compounds exhibit sensitization
1, 2-Di-3-thienyl-2-hydroxyethanone (3, 3′-thenoin).
Crundwell G, et al.
Acta Crystallographica Section E, Structure Reports Online, 58(6), o668-o670 (2002)
Kollur Shiva Prasad et al.
Molecules (Basel, Switzerland), 25(12) (2020-06-26)
Herein we report the synthesis and structural elucidation of two novel imine-based ligands, 2-(1,10-phenanthrolin-5-yl)imino)methyl)-5-bromophenol (PIB) and N-(1,10-phenanthrolin-5-yl)-1-(thiophen-3-yl)methanimine (PTM) ligands. An in vitro cytotoxicity assay of the synthesized molecules was carried out against breast, cervical, colorectal, and prostate cancer cell lines
Kyungsil Yoon et al.
Cells, 8(3) (2019-03-15)
Chicken ovalbumin upstream promoter-transcription factor I (COUP-TFI) is an orphan receptor and member of the nuclear receptor superfamily. Among a series of methylene substituted diindolylmethanes (C-DIMs) containing substituted phenyl and heteroaromatic groups, we identified 1,1-bis(3'-indolyl)-1-(4-pyridyl)-methane (DIM-C-Pyr-4) as an activator of
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