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196282

3-Thiophenecarboxaldehyde

Name: 3-Thiophenecarboxaldehyde
Brand: ALDRICH

98%

Synonym(s):

3-Formylthiophene, 3-Thienaldehyde, 3-Thienylcarboxaldehyde, 3-Thiophenealdehyde, 3-Thiophenecarbaldehyde, Thiofuran-3-carboxaldehyde, Thiophen-3-aldehyde

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About This Item

Empirical Formula (Hill Notation):

C₅H₄OS

CAS Number:

498-62-4

Molecular Weight:

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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Properties

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

Description

Application

3-Thiophenecarboxaldehyde has been used in the synthesis of:

series of 4-substituted 2-thiophenesulfonamides
acetal and ketal derivatives of 4′-demethylepipodophyllotoxin-β-D-glucoside and epipodophyllotoxin-β-D-glucoside
1,2-di-3-thienyl-2-hydroxyethanone (3,3′-thenoin), 3-thienyl symmetric analog of benzoin

pictograms

GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

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

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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

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

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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Global Trade Item Number

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