196282
3-噻吩甲醛
98%
别名:
3-噻吩甲醛, 3-噻吩醛, 3-甲醛噻吩, 噻吩-3-甲醛, 硫呋喃-3-甲醛
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关于此项目
经验公式（希尔记法）:
C5H4OS
化学文摘社编号:
分子量:
112.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-865-5
Beilstein/REAXYS Number:
105889
MDL number:
产品名称
3-噻吩甲醛, 98%
InChI key
RBIGKSZIQCTIJF-UHFFFAOYSA-N
InChI
1S/C5H4OS/c6-3-5-1-2-7-4-5/h1-4H
SMILES string
[H]C(=O)c1ccsc1
vapor pressure
0.31 mmHg ( 20 °C)
assay
98%
form
liquid
autoignition temp.
>392 °F
refractive index
n20/D 1.583 (lit.)
bp
194-196 °C (lit.)
86-87 °C/20 mmHg (lit.)
density
1.28 g/mL at 25 °C (lit.)
functional group
aldehyde
storage temp.
2-8°C
Quality Level
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Application
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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