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196282

3-噻吩甲醛

Name: 3-噻吩甲醛
Brand: ALDRICH

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:

498-62-4

分子量:

112.15

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24851749

EC Number:

207-865-5

Beilstein/REAXYS Number:

105889

MDL number:

MFCD00005466

Assay:

98%

Form:

liquid

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属性

vapor pressure

0.31 mmHg ( 20 °C)

Quality Level

100

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

SMILES string

[H]C(=O)c1ccsc1

InChI

1S/C5H4OS/c6-3-5-1-2-7-4-5/h1-4H

InChI key

RBIGKSZIQCTIJF-UHFFFAOYSA-N

说明

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

pictograms

GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

167.0 °F - closed cup

flash_point_c

75 °C - closed cup

ppe

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Synthesis and carbonic anhydrase inhibitory activity of 4-substituted 2-thiophenesulfonamides.

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

Synthesis and structure-activity relationships among glycosidic derivatives of 4'-demethylepipodophyllotoxin and epipodophyllotoxin, showing VM26- and VP16-213-like activities.

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

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)

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全球贸易项目编号

货号	GTIN
196282-1G	04061838096401
196282-10G	04061838762009
196282-5G	04061838089960